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3D Bioprinting Market Size to Touch Valuation of $1.5 Billion by 2028 | Inkjet Technology Generates More than 38% Revenue of Bioprinting Market -…

Posted: October 13, 2022 at 2:31 am

WASHINGTON, Oct. 09, 2022 (GLOBE NEWSWIRE) -- Global 3D bioprinting market was valued at USD 1.5 Billion in 2021 and is projected to attain a value of USD 3.7 Billion by 2028 during the forecast period, 20222028.

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As the demand for bioprinting continues to increase, so too does the need for 3D bioprinting. 3D bioprinting market uses small droplets of cell-containing material to create 3D objects in vitro It is useful for creating organs, tissues, and other structures from stem cells or other cells. It is also useful for creating customized implants and drugs.

The growing demand for 3D bioprinting has led to the development of new technologies and processes that make it easier and faster to create 3D objects. As the technology opens up new opportunities for the development of novel medical treatments, 3D bioprinting market growth is being driven by the increasing demand for personalized medicine, as well as the increasing need for customized structures and therapies. With each passing year, the technology is also becoming more affordable and accessible, making it an attractive option for clinical applications. This growth in demand will likely continue to accelerate in the future, as further advances in technology are made.

Top Players in Global 3D Bioprinting Market

Bioprinting is booming as a technology for creating tissue and organ replacement parts. The following are three factors driving demand for this innovative technology:

1. Growing aging population: The worlds population is growing older, which means there will be an increasing need for tissue and organ replacements. Bioprinting can help to fill this need by creating replacement tissues and organs from patient-specific cells. Over 1 billion people are above 60 years old and the number is projected to expand to 1.4 billion by 2050.

2. Declining supplies of natural organs and tissues: The availability of natural organs and tissues for transplantation is dwindling in worldwide 3D bioprinting market due to the increasing incidence of diseases such as Alzheimers, heart failure, and cancer. By using bioprinting, hospitals can create replacement tissues or organs specifically tailored to the needs of individual patients.

3. Progress in regenerative medicine: Regenerative medicine utilizes techniques such as cell therapy and 3D printing to restore function to damaged or diseased tissue. By printing tissue components in a controlled environment, regenerative medicine providers are able to engineers complex tissue constructs that would otherwise be extremely difficult or impossible to achieve.

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Increasing Adoption of 3D Bioprinting for Engineering Organs

3D bioprinting market is becoming an increasingly important as it enables the rapid, low-cost fabrication of complex components and structures from a variety of biocompatible materials. Vantage Market Research estimates that global spending on 3D printing services will top $2.3 billion by 2025, with growth rates well above the average for all software categories over the same period.

3D bioprinting market currently has niche applications in large-scale industrial production, but its potential to create low-cost human tissues and organs has drawn considerable interest. This is due in part to the high degree of customization that is possible with 3D bioprinting, which can enable precise control over tissue properties, including shape, size, and composition.

Every year, more than 10,000 Americans are put on waiting list for organ transplantation and over 6,000 of them die due to shortage or inability to get the suitable donor. This represents a huge opportunity for the players active in the global 3D bioprinting market to incentivize this revenue opportunity by engineering organ at scale to meet the demand and supply gap.

In fact, bioprinting is an emerging technology that enables the printing of nearly any type of biological tissue and organ. This technology has already been used to create structures such as heart valves, skin patches, and bone implants. However, there are still many applications for bioprinting that have yet to be explored.

3D printing is revolutionizing the way products are designed, and it is now being used to create organs at scale. By printing organs in a customized manner, we can improve the accuracy, predictability, and efficiency of organ printing.

There are many different types of organs that could benefit from bioprinting. Examples of organs that could be printed using this technology include lungs, liver, kidneys, and hearts. With bioprinting, surgeons could potentially print new organs onsite if they become damaged or diseased.

The applications for 3D bioprinting market are endless, and we are just starting to scratch the surface of what this technology can do. We believe that bioprinting will play a major role in engineering organ at scale in the future.

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As per Vantage Market Research, end-users and scientist have started paying attention to making use of 3D bioprinting on large scale thanks to numerous benefits of using 3D bioprinting for organ engineering. Some of the most important benefits include:

Browse market data Tables and Figures spread through 176 Pages and in-depth TOC on "3d Bioprinting Market by Technology (Inkjet-based, Magnetic Levitation, Syringe-based, Laser-based), by Application (Medical, Dental, Biosensors, Consumer/Personal Product Testing), by Region (North America, Latin America, Europe, Asia Pacific) - Global Industry Assessment (2016 - 2021) & Forecast (2022 - 2028)".

Inkjet Technology Generates More than 38% Revenue of Bioprinting Market

3D bioprinting market is becoming popular due to its versatility and ability to create complex tissue structures. However, one disadvantage of 3D bioprinting is the need for magnetic levitation technology in order to print large objects. Inkjet technology is becoming more popular for 3D bioprinting due to its lower printing costs and the ability to print larger objects. Inject technology uses a syringe filled with liquid bioprinters to create realistic tissue constructs.

Some of the biggest advantages of inkjet technology in the global 3D bioprinting market include its low cost and the ability to print complex tissue constructs. Inkjet printers can also produce large quantities of tissue at once, which makes them ideal for medical applications. Deploying inject printers in hospitals could improve the quality of patient care by allowing for faster production of customized tissue constructs. In addition, inject printers could help to reduce the cost of healthcare by reducing the need for magnetic levitation technology.

As per Vantage Market Research, most of the users in the global 3D bioprinting market prefer inkjet bioprinting technology because the printing can be faster and more accurate than magnetic levitation printing. Second, inkjet printing does not require the use of a cold bed or vacuum chamber both of which can be time-consuming and expensive to set up. Third, inkjet printing is less likely to produce errors due to materials incompatibility than magnetic levitation printing. Inkjet printing is also better at reproducing delicate features and patterns than magnetic levitation printing.

Overall, inkjet technology is becoming more popular for 3D bioprinting due to its speed, accuracy, and versatility.

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3D Bioprinting Market Size to Touch Valuation of $1.5 Billion by 2028 | Inkjet Technology Generates More than 38% Revenue of Bioprinting Market -...

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SANUWAVE’s Energy First Technology to be Featured in 3 Clinical Posters at Upcoming 2022 Fall Symposium on Advanced Wound Care (SAWC) -…

Posted: October 13, 2022 at 2:31 am

EDEN PRAIRIE, MN, Oct. 12, 2022 (GLOBE NEWSWIRE) -- via NewMediaWire SANUWAVE Health, Inc. (OTCPK: SNWV), a leading provider of next-generation wound care products, is excited to announce that three abstracts highlighting the role of the companys dermaPACE system in clinical cases were accepted to the Poster Presentation Hall at the upcoming 2022 Fall Symposium on Advanced Wound Care (SAWC) hosted by HMP Global. The conference is one of wound cares most esteemed events and will take place at Caesars Palace, Las Vegas, Nevada from October 13-16, 2022.

The following clinical cases, which examine the use of dermaPACE in patients with chronic, complex, and challenging wounds, will be presented.

1.) The Use of Non-Invasive Extracorporeal Shockwave Therapy (ESWT) Pulsed Acoustic Cellular Expression (PACE) System In Complex Wounds Related To Erythromelalgia, A Rare Skin Condition.

Dr. Marcelo de Oliveira e Silva, HOSPITAL CAXIAS DOR RIO DE JANEIRO general and plastic surgeon, UNIFESP Medical School Professor, Pontifical Catholic University (PUC) Carlos Chagas Medical Graduate Institute, coordinator, Quinta D'Or Hospital, specialist, evaluator, Brazilian Society of Plastic Surgery (SBCP), preceptor, Ivo Pitanguy Institute.

Dr. Paulo Roberto Castelleti Liborio Da Costa Brazilian Society of Plastic Surgery and Ivo Pitanguy Institute. Practices at Salgado Filho Municipal Hospital (Trauma Surgery,General Surgery) and Duque de Caxias DOr Hospital as Plastic Surgeon

2.) Extracorporeal Shockwave Therapy (ESWT) PACE-Technology: Pilot Trial to Treat Mixed Etiologies Lower Leg Ulcer in a Mobile Setting; When All Else Failed

John David Thomas, MD, FAPWCA Medical Director Solutions Medical Group, PLLC, Houston, TX. DIRECTOR OF WOUND CARE: Signature Home Health Baytown, TX; The Heights of North Houston Spring, TX; Park Manor, The Woodlands The Woodlands, TX; IPR Healthcare Systems Houston, TX; Crimson Heights Humble, TX. SPEAKER: Kerecis Omega3 Fish Skin technology. FORMER-SPEAKER: Acelity / KCI San Antonio, TX; Tissue Regenix Woundcare Inc. San Antonio, TX

3.) Extracorporeal Shockwave Therapy (ESWT) Pace-Technology: A New Approach to an Old Nemesis-Pyoderma Gangrenosum

Dr Perry Mayer; Medical Director of The Mayer Institute (TMI), Center of Excellence Hamilton Ontario Canada

Representatives from SANUWAVE will be available at SAWC booth #619 in the exhibit hall for inquiries on their ENERGY FIRST product portfolio which includes both dermaPACE and UltraMIST. The companys CEO, Kevin Richardson, and CRO, Jack Schlechtweg, will also be in attendance.

If you are attending the event and would like to schedule some time to meet with a team member, please email the companys Marketing contact Sabrina Ruelle at Sabrina.Ruelle@Sanuwave.com so she can help facilitate a meet time.

Additional information regarding SANWUAVEs product portfolio is available through their website at https://sanuwave.com/

About SANUWAVE

SANUWAVE Health is focused on the research, development, and commercialization of its patented, non-invasive and biological response-activating medical systems for the repair and regeneration of skin, musculoskeletal tissue, and vascular structures.

SANUWAVEs end-to-end wound care portfolio of regenerative medicine products and product candidates help restore the bodys normal healing processes. SANUWAVE applies and researches its patented energy transfer technologies in wound healing, orthopedic/spine, aesthetic/cosmetic, and cardiac/endovascular conditions.

Forward-Looking Statements

This press release may contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, such as statements relating to financial results and plans for future business development activities and are thus prospective. Forward-looking statements include all statements that are not statements of historical fact regarding intent, belief or current expectations of the Company, its directors or its officers. Investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, many of which are beyond the Companys ability to control. Actual results may differ materially from those projected in the forward-looking statements. Among the key risks, assumptions and factors that may affect operating results, performance and financial condition are risks associated with the regulatory approval and marketing of the Companys product candidates and products, unproven pre-clinical and clinical development activities, regulatory oversight, the Companys ability to manage its capital resource issues, competition, and the other factors discussed in detail in the Companys periodic filings with the Securities and Exchange Commission. The Company undertakes no obligation to update any forward-looking statement.

INVESTOR RELATIONS CONTACT:Investorrelations@Sanuwave.com

2022 GlobeNewswire, Inc., source Press Releases

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Stem Cell Therapy for Knees – thriveMD Denver & Vail, CO

Posted: October 13, 2022 at 2:30 am

Articular cartilage damage, especially when it affects the knee joint, remains a major clinical problem due to the poor intrinsic ability for this tissue to repair itself. The major function of joint cartilage is to allow for smooth gliding of joint surfaces and to protect the surrounding bone from stress. This sort of movement is key for individuals who participate in sports such as skiing. In a wider context, though, knee cartilage damage can prevent people from running, exercising, or just moving as freely as theyd like. Articular cartilage allows the knee to absorb shock and loads up to 20 times the body weight.

There are many reasons why someone may experience articular knee cartilage damage. Regular wear and tear on the knee over time, involvement in high-stress activities, or accidents and injuries can all contribute to cartilage damage around the knee joint.

Osteoarthritis is a chronic degenerative disorder that ultimately leads to a gradual deterioration of knee joint cartilage. Osteoarthritis may also be the result of a prior injury to the knee joint such as a fracture, tendon damage, or ligament tears.

This may lead to joint instability, which can cause long-term damage to the articular cartilage. Arthritis can affect not only the cartilage but may also lead to damage of the bone beneath the cartilage, the synovial lining to the joint, ligaments, tendons, and muscles.

Adult stem cells are incredibly versatile in a medical sense. They have a potential to reliably differentiate into cartilage, bone, fat, or soft tissue. Because of this, the injection of progenitor cells, especially mesenchymal stem cells (special stem cells from adipose tissue or bone marrow), have been shown to be a better strategy to repair degenerative cartilage than implantation of differentiated cells such as articular cartilage.

In other words, when adult stem cells are injected into a knee with damaged cartilage, they can act to repair damaged tissue and build new cartilage.

Adult stem cells also display the ability to specifically address areas of inflammation and degeneration and to modify immune system activity, which can favorably influence the surrounding cartilage in areas of damage.

Encouragingly, results of pre-clinical and clinical trials have provided initial evidence of efficacy and safety in the therapeutic use of mesenchymal stem cell therapies for the treatment of knee cartilage damage and osteoarthritis. Cell-based therapy has become a key priority of tissue engineering research focused on functional replacement of cartilage and meniscus regeneration.

A year long animal study has provided research that demonstrates that stem cell treatments provide structural regeneration with mechanical properties comparable with the native cartilage.

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Stem cell therapy and autism | Raising Children Network

Posted: October 13, 2022 at 2:30 am

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Cellectis Presents Data on Two TALEN-based Gene Therapy Preclinical Programs for Patients with … – The Bakersfield Californian

Posted: October 13, 2022 at 2:30 am

NEW YORK, Oct. 11, 2022 (GLOBE NEWSWIRE) -- Cellectis (the Company) (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies, announced today that the Company will present both an oral and poster at the European Society of Gene and Cell Therapys (ESGCT) 29th Congress, to be held in Edinburgh from October 11-14, 2022.

Arianna Moiani, Ph.D., Senior Scientist & Team Leader Innovation Gene Therapy, will give an oral presentation on encouraging pre-clinical data that leverages TALEN gene editing technology to develop a hematopoietic stem and progenitor cell (HSPCs)-based gene therapy to treat sickle cell disease.

Eduardo Seclen, Ph.D., Senior Scientist & Team Leader, Gene Editing, will present a poster illustrating a TALEN-based gene editing approach that reprograms HSPCs to secrete alpha-L-iduronidase (IDUA), a therapeutic enzyme missing in Mucopolysaccharidosis type I (MPS-I).

The pre-clinical data presented at ESGCT further demonstrate our ability to leverage TALEN gene editing technology to potentially address genetic diseases, namely, sickle cell disease and lysosomal storage diseases. By correcting a faulty mutation or inserting a corrected gene at the HSPC level, we aim to provide a lifelong supply of healthy cells in a single intervention, said Philippe Duchateau, Ph.D., Chief Scientific Officer at Cellectis. These new milestones bring us one step closer to our goal: providing a cure to patients that have failed to respond to standard therapy.

Presentation details

Pre-clinical data presentation on a non-viral DNA delivery associated with TALEN gene editing that leads to highly efficient correction of sickle cell mutation in long-term repopulating hematopoietic stem cells

Sickle cell disease stems from a single point mutation in the HBB gene which results in sickle hemoglobin.

Cellectis leveraged its TALEN technology to develop a gene editing process that leads to highly efficient HBB gene correction via homology directed repair, while mitigating potential risks associated to HBB gene knock-out.

Overall, these results show that non-viral DNA delivery associated with TALEN gene editing reduces the toxicity usually observed with viral DNA delivery and allows high levels of HBB gene correction in long-term repopulating hematopoietic stem cells.

The oral presentation titled Non-viral DNA delivery associated to TALEN gene editing leads to highly efficient correction of sickle cell mutation in long-term repopulating hematopoietic stem cells, will be made on Thursday, October 13th, 8:30AM-10:45AM BST by Arianna Moiani, Ph.D., Senior Scientist & Team Leader Innovation Gene Therapy. The presentation can be found on the Cellectis website on the day of the presentation.

Presentation details

Pre-clinical data presentation on TALEN-mediated engineering of HSPC that enables systemic delivery of IDUA

Mucopolysaccharidosis type I (MPS-I) is caused by deficiencies in the alpha-L-iduronidase (IDUA) gene and it is associated with severe morbidity representing a significant unmet medical need.

Cellectis established a TALEN-based ex vivo gene editing protocol to insert an IDUA-expression cassette into a specific locus of HSPC.

Editing rates in vivo were 6-9% sixteen weeks after injection, depending on the tissue analyzed (blood, spleen, bone marrow). Lastly, 8.3% of human cells were edited in the brain compartment.

Cellectis established a safe TALEN-based gene editing protocol procuring IDUA-edited HSPCs able to engraft, differentiate into multiple lineages and reach multiple tissues, including the brain.

The poster presentation titled TALEN-mediated engineering of HSPC enables systemic delivery of IDUA, will be made on Thursday, October 13th, 5:30PM - 7:15PM BST by Eduardo Seclen, Ph.D., Senior Scientist & Team Leader, Gene Editing, and can be found on Cellectis website.

About Cellectis

Cellectis is a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies. Cellectis utilizes an allogeneic approach for CAR-T immunotherapies in oncology, pioneering the concept of off-the-shelf and ready-to-use gene-edited CAR T-cells to treat cancer patients, and a platform to make therapeutic gene editing in hemopoietic stem cells for various diseases. As a clinical-stage biopharmaceutical company with over 22 years of experience and expertise in gene editing, Cellectis is developing life-changing product candidates utilizing TALEN, its gene editing technology, and PulseAgile, its pioneering electroporation system to harness the power of the immune system in order to treat diseases with unmet medical needs. Cellectis headquarters are in Paris, France, with locations in New York, New York and Raleigh, North Carolina. Cellectis is listed on the Nasdaq Global Market (ticker: CLLS) and on Euronext Growth (ticker: ALCLS).

For more information, visit http://www.cellectis.com. Follow Cellectis on social media: @cellectis, LinkedIn and YouTube.

For further information, please contact:

Media contacts:

Pascalyne Wilson,Director,Communications,+33 (0)7 76 99 14 33, media@cellectis.com

Margaret Gandolfo, Senior Manager, Communications, +1 (646) 628 0300

Investor Relation contact:

Arthur Stril, Chief Business Officer, +1 (347) 809 5980, investors@cellectis.com

Ashley R. Robinson, LifeSci Advisors, +1 617430 7577

Forward-looking Statements

This press release contains forward-looking statements within the meaning of applicable securities laws, including the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by words such as anticipate, believe, intend, expect, plan, scheduled, could, may and will, or the negative of these and similar expressions. These forward-looking statements, which are based on our managements current expectations and assumptions and on information currently available to management. Forward-looking statements include statements about the potential of our preclinical programs and product candidates. These forward-looking statements are made in light of information currently available to us and are subject to numerous risks and uncertainties, including with respect to the numerous risks associated with biopharmaceutical product candidate development. With respect to our cash runway, our operating plans, including product development plans, may change as a result of various factors, including factors currently unknown to us. Furthermore, many other important factors, including those described in our Annual Report on Form 20-F and the financial report (including the management report) for the year ended December 31, 2021 and subsequent filings Cellectis makes with the Securities Exchange Commission from time to time, as well as other known and unknown risks and uncertainties may adversely affect such forward-looking statements and cause our actual results, performance or achievements to be materially different from those expressed or implied by the forward-looking statements. Except as required by law, we assume no obligation to update these forward-looking statements publicly, or to update the reasons why actual results could differ materially from those anticipated in the forward-looking statements, even if new information becomes available in the future.

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Global Nerve Repair and Regeneration Devices Market to Reach $12.9 Billion by 2027 – Yahoo Finance

Posted: October 13, 2022 at 2:30 am

ReportLinker

Abstract: Whats New for 2022?? Global competitiveness and key competitor percentage market shares. Market presence across multiple geographies - Strong/Active/Niche/Trivial.

New York, Oct. 11, 2022 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Global Nerve Repair and Regeneration Devices Industry" - https://www.reportlinker.com/p05957490/?utm_source=GNW

Online interactive peer-to-peer collaborative bespoke updates

Access to our digital archives and MarketGlass Research Platform

Complimentary updates for one yearGlobal Nerve Repair and Regeneration Devices Market to Reach $12.9 Billion by 2027- In the changed post COVID-19 business landscape, the global market for Nerve Repair and Regeneration Devices estimated at US$6.6 Billion in the year 2020, is projected to reach a revised size of US$12.9 Billion by 2027, growing at aCAGR of 10% over the period 2020-2027. Neurostimulation & Neuromodulation Devices, one of the segments analyzed in the report, is projected to record 9.7% CAGR and reach US$10.9 Billion by the end of the analysis period. Taking into account the ongoing post pandemic recovery, growth in the Biomaterials segment is readjusted to a revised 11.7% CAGR for the next 7-year period.- The U.S. Market is Estimated at $2 Billion, While China is Forecast to Grow at 13% CAGR- The Nerve Repair and Regeneration Devices market in the U.S. is estimated at US$2 Billion in the year 2020. China, the world`s second largest economy, is forecast to reach a projected market size of US$2 Billion by the year 2027 trailing a CAGR of 13% over the analysis period 2020 to 2027. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at 7.7% and 8.8% respectively over the 2020-2027 period. Within Europe, Germany is forecast to grow at approximately 9.2% CAGR.

Select Competitors (Total 61 Featured)Abbott Laboratories, Inc.AxoGen, Inc.Boston Scientific CorporationIntegra LifeSciences CorporationLivaNova, PLCMedtronic plcNeuroPace, Inc.Nevro Corporation.Orthomed S.A.S.Polyganics B.V.Stryker CorporationSynapse Biomedical Inc.Synovis Micro Companies Alliance, Inc.

Read the full report: https://www.reportlinker.com/p05957490/?utm_source=GNW

I. METHODOLOGY

II. EXECUTIVE SUMMARY1. GLOBAL MARKET OVERVIEWImpact of Covid-19 and a Looming Global Recession2020 Marked as a Year of Disruption & TransformationWorld Economic Growth Projections (Real GDP, Annual % Change)for 2019 to 2022Global Nerve Repair & Regeneration Market Buckles under COVID-19 StrainCovid-19 Patients in Prone Position Suffering Nerve DamageBodes Well for Market GrowthNerve Repair and Regeneration Market Set for a Robust GrowthNeurostimulation & Neuromodulation Devices Hold Commanding Slotin Nerve Repair & Regeneration MarketBiomaterials to Exhibit Rapid GrowthNerve Repair and Regeneration Market by ApplicationUS and Europe Dominate the MarketAsia-Pacific and other Emerging Regions Display ImpressiveGrowth PotentialRecent Market Activity

2. FOCUS ON SELECT PLAYERS

3. MARKET TRENDS & DRIVERSHigh Incidence of Neurological Disorders: A Key Market DriverAnnual Incidence of Adult-Onset Neurologic Disorders in the USEffects of COVID-19 on the Nervous System Sheds Focus onNeuromodulation ApplicationsIncreasing Cases of Peripheral Nerve Injuries Drive the NerveRepair and Regeneration MarketGrowing Number of Vehicular Accidents Drive the PeripheralNerve injuries Repair MarketRising Geriatric Population and Subsequent Growth in PrevalenceOf Neurological DisordersGlobal Population Statistics for the 65+ Age Group in Millionby Geographic Region for the Years 2019, 2025, 2035 and 2050Growing Incidence of Neurodegenerative Diseases Propels theMarket for Deep Brain Stimulation DevicesGlobal Alzheimers Prevalence by Age GroupDiagnosed Prevalence Cases of Parkinson?s Disease Across SelectCountriesGlobal DBS Market by Leading Player (2020E): Market ShareBreakdown of Revenues for Medtronic, Boston Scientific, andAbbottSelect Available Deep Brain Stimulation Devices Available inthe MarketIntensified Research Activity Across Various Neural DisciplinesInduces Additional OptimismStem Cell Therapy: A Promising Avenue for Nerve Repair andRegenerationIncreasing Cases of Epilepsy Drives the Demand for Vagus NerveStimulation DevicesEpilepsy Incidence by Type (2019): Percentage Share Breakdownfor Idiopathic and Symptomatic EpilepsySymptomatic Epilepsy Incidence by Type (2019): Percentage ShareBreakdown of Congenital, Degenerative, Infective, Neoplastic,Trauma, and Vascular EpilepsySpinal Cord Injuries Propel the Demand for Spinal CordStimulation DevicesRecent Developments in Spinal Cord Injury TreatmentBiomaterials (Nerve Conduits and Nerve Wraps) to Witness RapidGrowthNew Biomaterials Pave the Way for Innovative NeurodegenerationTherapiesRole of Nerve Conduits in the Treatment of Peripheral Nerve InjuryInnovative Nerve Conduits from StrykerTENS (Transcutaneous electrical nerve stimulation devices)Market Witnesses Rapid GrowthNon-Invasiveness of TMS (Transcranial Magnetic Stimulation)Propelling the adoption of TMS devicesNerve Grafts for Bridging Larger Nerve GapsRole of Nerve Grafting in Treatment of Peripheral Nerve InjuriesFDA-approved Nerve Tubes for Peripheral Nerve Repair

4. GLOBAL MARKET PERSPECTIVETable 1: World Recent Past, Current & Future Analysis for NerveRepair and Regeneration Devices by Geographic Region - USA,Canada, Japan, China, Europe, Asia-Pacific, Latin America,Middle East and Africa Markets - Independent Analysis of AnnualSales in US$ Thousand for Years 2020 through 2027 and % CAGR

Table 2: World Historic Review for Nerve Repair andRegeneration Devices by Geographic Region - USA, Canada, Japan,China, Europe, Asia-Pacific, Latin America, Middle East andAfrica Markets - Independent Analysis of Annual Sales in US$Thousand for Years 2012 through 2019 and % CAGR

Table 3: World 15-Year Perspective for Nerve Repair andRegeneration Devices by Geographic Region - PercentageBreakdown of Value Sales for USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa Markets forYears 2012, 2021 & 2027

Table 4: World Recent Past, Current & Future Analysis forNeurostimulation & Neuromodulation Devices by Geographic Region -USA, Canada, Japan, China, Europe, Asia-Pacific, LatinAmerica, Middle East and Africa Markets - Independent Analysisof Annual Sales in US$ Thousand for Years 2020 through 2027and % CAGR

Table 5: World Historic Review for Neurostimulation &Neuromodulation Devices by Geographic Region - USA, Canada,Japan, China, Europe, Asia-Pacific, Latin America, Middle Eastand Africa Markets - Independent Analysis of Annual Sales inUS$ Thousand for Years 2012 through 2019 and % CAGR

Table 6: World 15-Year Perspective for Neurostimulation &Neuromodulation Devices by Geographic Region - PercentageBreakdown of Value Sales for USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa for Years2012, 2021 & 2027

Table 7: World Recent Past, Current & Future Analysis forBiomaterials by Geographic Region - USA, Canada, Japan, China,Europe, Asia-Pacific, Latin America, Middle East and AfricaMarkets - Independent Analysis of Annual Sales in US$ Thousandfor Years 2020 through 2027 and % CAGR

Table 8: World Historic Review for Biomaterials by GeographicRegion - USA, Canada, Japan, China, Europe, Asia-Pacific, LatinAmerica, Middle East and Africa Markets - Independent Analysisof Annual Sales in US$ Thousand for Years 2012 through 2019and % CAGR

Table 9: World 15-Year Perspective for Biomaterials byGeographic Region - Percentage Breakdown of Value Sales forUSA, Canada, Japan, China, Europe, Asia-Pacific, Latin America,Middle East and Africa for Years 2012, 2021 & 2027

Table 10: World Recent Past, Current & Future Analysis forNeurostimulation & Neuromodulation Surgeries by GeographicRegion - USA, Canada, Japan, China, Europe, Asia-Pacific, LatinAmerica, Middle East and Africa Markets - Independent Analysisof Annual Sales in US$ Thousand for Years 2020 through 2027and % CAGR

Table 11: World Historic Review for Neurostimulation &Neuromodulation Surgeries by Geographic Region - USA, Canada,Japan, China, Europe, Asia-Pacific, Latin America, Middle Eastand Africa Markets - Independent Analysis of Annual Sales inUS$ Thousand for Years 2012 through 2019 and % CAGR

Table 12: World 15-Year Perspective for Neurostimulation &Neuromodulation Surgeries by Geographic Region - PercentageBreakdown of Value Sales for USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa for Years2012, 2021 & 2027

Table 13: World Recent Past, Current & Future Analysis forNeurorrhaphy by Geographic Region - USA, Canada, Japan, China,Europe, Asia-Pacific, Latin America, Middle East and AfricaMarkets - Independent Analysis of Annual Sales in US$ Thousandfor Years 2020 through 2027 and % CAGR

Table 14: World Historic Review for Neurorrhaphy by GeographicRegion - USA, Canada, Japan, China, Europe, Asia-Pacific, LatinAmerica, Middle East and Africa Markets - Independent Analysisof Annual Sales in US$ Thousand for Years 2012 through 2019and % CAGR

Table 15: World 15-Year Perspective for Neurorrhaphy byGeographic Region - Percentage Breakdown of Value Sales forUSA, Canada, Japan, China, Europe, Asia-Pacific, Latin America,Middle East and Africa for Years 2012, 2021 & 2027

Table 16: World Recent Past, Current & Future Analysis forNerve Grafting by Geographic Region - USA, Canada, Japan,China, Europe, Asia-Pacific, Latin America, Middle East andAfrica Markets - Independent Analysis of Annual Sales in US$Thousand for Years 2020 through 2027 and % CAGR

Table 17: World Historic Review for Nerve Grafting byGeographic Region - USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa Markets -Independent Analysis of Annual Sales in US$ Thousand for Years2012 through 2019 and % CAGR

Table 18: World 15-Year Perspective for Nerve Grafting byGeographic Region - Percentage Breakdown of Value Sales forUSA, Canada, Japan, China, Europe, Asia-Pacific, Latin America,Middle East and Africa for Years 2012, 2021 & 2027

Table 19: World Recent Past, Current & Future Analysis for StemCell Therapy by Geographic Region - USA, Canada, Japan, China,Europe, Asia-Pacific, Latin America, Middle East and AfricaMarkets - Independent Analysis of Annual Sales in US$ Thousandfor Years 2020 through 2027 and % CAGR

Table 20: World Historic Review for Stem Cell Therapy byGeographic Region - USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa Markets -Independent Analysis of Annual Sales in US$ Thousand for Years2012 through 2019 and % CAGR

Table 21: World 15-Year Perspective for Stem Cell Therapy byGeographic Region - Percentage Breakdown of Value Sales forUSA, Canada, Japan, China, Europe, Asia-Pacific, Latin America,Middle East and Africa for Years 2012, 2021 & 2027

Table 22: World Recent Past, Current & Future Analysis forHospitals & Clinics by Geographic Region - USA, Canada, Japan,China, Europe, Asia-Pacific, Latin America, Middle East andAfrica Markets - Independent Analysis of Annual Sales in US$Thousand for Years 2020 through 2027 and % CAGR

Table 23: World Historic Review for Hospitals & Clinics byGeographic Region - USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa Markets -Independent Analysis of Annual Sales in US$ Thousand for Years2012 through 2019 and % CAGR

Table 24: World 15-Year Perspective for Hospitals & Clinics byGeographic Region - Percentage Breakdown of Value Sales forUSA, Canada, Japan, China, Europe, Asia-Pacific, Latin America,Middle East and Africa for Years 2012, 2021 & 2027

Table 25: World Recent Past, Current & Future Analysis forAmbulatory Surgery Centers by Geographic Region - USA, Canada,Japan, China, Europe, Asia-Pacific, Latin America, Middle Eastand Africa Markets - Independent Analysis of Annual Sales inUS$ Thousand for Years 2020 through 2027 and % CAGR

Table 26: World Historic Review for Ambulatory Surgery Centersby Geographic Region - USA, Canada, Japan, China, Europe,Asia-Pacific, Latin America, Middle East and Africa Markets -Independent Analysis of Annual Sales in US$ Thousand for Years2012 through 2019 and % CAGR

Table 27: World 15-Year Perspective for Ambulatory SurgeryCenters by Geographic Region - Percentage Breakdown of ValueSales for USA, Canada, Japan, China, Europe, Asia-Pacific,Latin America, Middle East and Africa for Years 2012, 2021 &2027Impact of Covid-19 and a Looming Global Recession

III. MARKET ANALYSIS

UNITED STATESNerve Repair and Regeneration Devices Market Presence - Strong/Active/Niche/Trivial - Key Competitors in the United Statesfor 2022 (E)Table 28: USA Recent Past, Current & Future Analysis for NerveRepair and Regeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 29: USA Historic Review for Nerve Repair and RegenerationDevices by Product - Neurostimulation & Neuromodulation Devicesand Biomaterials Markets - Independent Analysis of Annual Salesin US$ Thousand for Years 2012 through 2019 and % CAGR

Table 30: USA 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

Table 31: USA Recent Past, Current & Future Analysis for NerveRepair and Regeneration Devices by Application -Neurostimulation & Neuromodulation Surgeries, Neurorrhaphy,Nerve Grafting and Stem Cell Therapy - Independent Analysis ofAnnual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 32: USA Historic Review for Nerve Repair and RegenerationDevices by Application - Neurostimulation & NeuromodulationSurgeries, Neurorrhaphy, Nerve Grafting and Stem Cell TherapyMarkets - Independent Analysis of Annual Sales in US$ Thousandfor Years 2012 through 2019 and % CAGR

Table 33: USA 15-Year Perspective for Nerve Repair andRegeneration Devices by Application - Percentage Breakdown ofValue Sales for Neurostimulation & Neuromodulation Surgeries,Neurorrhaphy, Nerve Grafting and Stem Cell Therapy for theYears 2012, 2021 & 2027

Table 34: USA Recent Past, Current & Future Analysis for NerveRepair and Regeneration Devices by End-Use - Hospitals &Clinics and Ambulatory Surgery Centers - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 35: USA Historic Review for Nerve Repair and RegenerationDevices by End-Use - Hospitals & Clinics and Ambulatory SurgeryCenters Markets - Independent Analysis of Annual Sales in US$Thousand for Years 2012 through 2019 and % CAGR

Table 36: USA 15-Year Perspective for Nerve Repair andRegeneration Devices by End-Use - Percentage Breakdown of ValueSales for Hospitals & Clinics and Ambulatory Surgery Centersfor the Years 2012, 2021 & 2027

CANADATable 37: Canada Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Product -Neurostimulation & Neuromodulation Devices and Biomaterials -Independent Analysis of Annual Sales in US$ Thousand for theYears 2020 through 2027 and % CAGR

Table 38: Canada Historic Review for Nerve Repair andRegeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials Markets - IndependentAnalysis of Annual Sales in US$ Thousand for Years 2012 through2019 and % CAGR

Table 39: Canada 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

Table 40: Canada Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Application -Neurostimulation & Neuromodulation Surgeries, Neurorrhaphy,Nerve Grafting and Stem Cell Therapy - Independent Analysis ofAnnual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 41: Canada Historic Review for Nerve Repair andRegeneration Devices by Application - Neurostimulation &Neuromodulation Surgeries, Neurorrhaphy, Nerve Grafting andStem Cell Therapy Markets - Independent Analysis of AnnualSales in US$ Thousand for Years 2012 through 2019 and % CAGR

Table 42: Canada 15-Year Perspective for Nerve Repair andRegeneration Devices by Application - Percentage Breakdown ofValue Sales for Neurostimulation & Neuromodulation Surgeries,Neurorrhaphy, Nerve Grafting and Stem Cell Therapy for theYears 2012, 2021 & 2027

Table 43: Canada Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by End-Use - Hospitals &Clinics and Ambulatory Surgery Centers - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 44: Canada Historic Review for Nerve Repair andRegeneration Devices by End-Use - Hospitals & Clinics andAmbulatory Surgery Centers Markets - Independent Analysis ofAnnual Sales in US$ Thousand for Years 2012 through 2019 and %CAGR

Table 45: Canada 15-Year Perspective for Nerve Repair andRegeneration Devices by End-Use - Percentage Breakdown of ValueSales for Hospitals & Clinics and Ambulatory Surgery Centersfor the Years 2012, 2021 & 2027

JAPANNerve Repair and Regeneration Devices Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Japan for 2022 (E)Table 46: Japan Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Product -Neurostimulation & Neuromodulation Devices and Biomaterials -Independent Analysis of Annual Sales in US$ Thousand for theYears 2020 through 2027 and % CAGR

Table 47: Japan Historic Review for Nerve Repair andRegeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials Markets - IndependentAnalysis of Annual Sales in US$ Thousand for Years 2012 through2019 and % CAGR

Table 48: Japan 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

Table 49: Japan Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Application -Neurostimulation & Neuromodulation Surgeries, Neurorrhaphy,Nerve Grafting and Stem Cell Therapy - Independent Analysis ofAnnual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 50: Japan Historic Review for Nerve Repair andRegeneration Devices by Application - Neurostimulation &Neuromodulation Surgeries, Neurorrhaphy, Nerve Grafting andStem Cell Therapy Markets - Independent Analysis of AnnualSales in US$ Thousand for Years 2012 through 2019 and % CAGR

Table 51: Japan 15-Year Perspective for Nerve Repair andRegeneration Devices by Application - Percentage Breakdown ofValue Sales for Neurostimulation & Neuromodulation Surgeries,Neurorrhaphy, Nerve Grafting and Stem Cell Therapy for theYears 2012, 2021 & 2027

Table 52: Japan Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by End-Use - Hospitals &Clinics and Ambulatory Surgery Centers - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 53: Japan Historic Review for Nerve Repair andRegeneration Devices by End-Use - Hospitals & Clinics andAmbulatory Surgery Centers Markets - Independent Analysis ofAnnual Sales in US$ Thousand for Years 2012 through 2019 and %CAGR

Table 54: Japan 15-Year Perspective for Nerve Repair andRegeneration Devices by End-Use - Percentage Breakdown of ValueSales for Hospitals & Clinics and Ambulatory Surgery Centersfor the Years 2012, 2021 & 2027

CHINANerve Repair and Regeneration Devices Market Presence - Strong/Active/Niche/Trivial - Key Competitors in China for 2022 (E)Table 55: China Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Product -Neurostimulation & Neuromodulation Devices and Biomaterials -Independent Analysis of Annual Sales in US$ Thousand for theYears 2020 through 2027 and % CAGR

Table 56: China Historic Review for Nerve Repair andRegeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials Markets - IndependentAnalysis of Annual Sales in US$ Thousand for Years 2012 through2019 and % CAGR

Table 57: China 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

Table 58: China Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Application -Neurostimulation & Neuromodulation Surgeries, Neurorrhaphy,Nerve Grafting and Stem Cell Therapy - Independent Analysis ofAnnual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 59: China Historic Review for Nerve Repair andRegeneration Devices by Application - Neurostimulation &Neuromodulation Surgeries, Neurorrhaphy, Nerve Grafting andStem Cell Therapy Markets - Independent Analysis of AnnualSales in US$ Thousand for Years 2012 through 2019 and % CAGR

Table 60: China 15-Year Perspective for Nerve Repair andRegeneration Devices by Application - Percentage Breakdown ofValue Sales for Neurostimulation & Neuromodulation Surgeries,Neurorrhaphy, Nerve Grafting and Stem Cell Therapy for theYears 2012, 2021 & 2027

Table 61: China Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by End-Use - Hospitals &Clinics and Ambulatory Surgery Centers - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 62: China Historic Review for Nerve Repair andRegeneration Devices by End-Use - Hospitals & Clinics andAmbulatory Surgery Centers Markets - Independent Analysis ofAnnual Sales in US$ Thousand for Years 2012 through 2019 and %CAGR

Table 63: China 15-Year Perspective for Nerve Repair andRegeneration Devices by End-Use - Percentage Breakdown of ValueSales for Hospitals & Clinics and Ambulatory Surgery Centersfor the Years 2012, 2021 & 2027

EUROPENerve Repair and Regeneration Devices Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Europe for 2022 (E)Table 64: Europe Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Geographic Region -France, Germany, Italy, UK, Spain, Russia and Rest of EuropeMarkets - Independent Analysis of Annual Sales in US$ Thousandfor Years 2020 through 2027 and % CAGR

Table 65: Europe Historic Review for Nerve Repair andRegeneration Devices by Geographic Region - France, Germany,Italy, UK, Spain, Russia and Rest of Europe Markets -Independent Analysis of Annual Sales in US$ Thousand for Years2012 through 2019 and % CAGR

Table 66: Europe 15-Year Perspective for Nerve Repair andRegeneration Devices by Geographic Region - PercentageBreakdown of Value Sales for France, Germany, Italy, UK, Spain,Russia and Rest of Europe Markets for Years 2012, 2021 & 2027

Table 67: Europe Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Product -Neurostimulation & Neuromodulation Devices and Biomaterials -Independent Analysis of Annual Sales in US$ Thousand for theYears 2020 through 2027 and % CAGR

Table 68: Europe Historic Review for Nerve Repair andRegeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials Markets - IndependentAnalysis of Annual Sales in US$ Thousand for Years 2012 through2019 and % CAGR

Table 69: Europe 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

Table 70: Europe Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Application -Neurostimulation & Neuromodulation Surgeries, Neurorrhaphy,Nerve Grafting and Stem Cell Therapy - Independent Analysis ofAnnual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 71: Europe Historic Review for Nerve Repair andRegeneration Devices by Application - Neurostimulation &Neuromodulation Surgeries, Neurorrhaphy, Nerve Grafting andStem Cell Therapy Markets - Independent Analysis of AnnualSales in US$ Thousand for Years 2012 through 2019 and % CAGR

Table 72: Europe 15-Year Perspective for Nerve Repair andRegeneration Devices by Application - Percentage Breakdown ofValue Sales for Neurostimulation & Neuromodulation Surgeries,Neurorrhaphy, Nerve Grafting and Stem Cell Therapy for theYears 2012, 2021 & 2027

Table 73: Europe Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by End-Use - Hospitals &Clinics and Ambulatory Surgery Centers - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 74: Europe Historic Review for Nerve Repair andRegeneration Devices by End-Use - Hospitals & Clinics andAmbulatory Surgery Centers Markets - Independent Analysis ofAnnual Sales in US$ Thousand for Years 2012 through 2019 and %CAGR

Table 75: Europe 15-Year Perspective for Nerve Repair andRegeneration Devices by End-Use - Percentage Breakdown of ValueSales for Hospitals & Clinics and Ambulatory Surgery Centersfor the Years 2012, 2021 & 2027

FRANCENerve Repair and Regeneration Devices Market Presence - Strong/Active/Niche/Trivial - Key Competitors in France for 2022 (E)Table 76: France Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Product -Neurostimulation & Neuromodulation Devices and Biomaterials -Independent Analysis of Annual Sales in US$ Thousand for theYears 2020 through 2027 and % CAGR

Table 77: France Historic Review for Nerve Repair andRegeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials Markets - IndependentAnalysis of Annual Sales in US$ Thousand for Years 2012 through2019 and % CAGR

Table 78: France 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

Table 79: France Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Application -Neurostimulation & Neuromodulation Surgeries, Neurorrhaphy,Nerve Grafting and Stem Cell Therapy - Independent Analysis ofAnnual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 80: France Historic Review for Nerve Repair andRegeneration Devices by Application - Neurostimulation &Neuromodulation Surgeries, Neurorrhaphy, Nerve Grafting andStem Cell Therapy Markets - Independent Analysis of AnnualSales in US$ Thousand for Years 2012 through 2019 and % CAGR

Table 81: France 15-Year Perspective for Nerve Repair andRegeneration Devices by Application - Percentage Breakdown ofValue Sales for Neurostimulation & Neuromodulation Surgeries,Neurorrhaphy, Nerve Grafting and Stem Cell Therapy for theYears 2012, 2021 & 2027

Table 82: France Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by End-Use - Hospitals &Clinics and Ambulatory Surgery Centers - Independent Analysisof Annual Sales in US$ Thousand for the Years 2020 through 2027and % CAGR

Table 83: France Historic Review for Nerve Repair andRegeneration Devices by End-Use - Hospitals & Clinics andAmbulatory Surgery Centers Markets - Independent Analysis ofAnnual Sales in US$ Thousand for Years 2012 through 2019 and %CAGR

Table 84: France 15-Year Perspective for Nerve Repair andRegeneration Devices by End-Use - Percentage Breakdown of ValueSales for Hospitals & Clinics and Ambulatory Surgery Centersfor the Years 2012, 2021 & 2027

GERMANYNerve Repair and Regeneration Devices Market Presence - Strong/Active/Niche/Trivial - Key Competitors in Germany for 2022:(E)Table 85: Germany Recent Past, Current & Future Analysis forNerve Repair and Regeneration Devices by Product -Neurostimulation & Neuromodulation Devices and Biomaterials -Independent Analysis of Annual Sales in US$ Thousand for theYears 2020 through 2027 and % CAGR

Table 86: Germany Historic Review for Nerve Repair andRegeneration Devices by Product - Neurostimulation &Neuromodulation Devices and Biomaterials Markets - IndependentAnalysis of Annual Sales in US$ Thousand for Years 2012 through2019 and % CAGR

Table 87: Germany 15-Year Perspective for Nerve Repair andRegeneration Devices by Product - Percentage Breakdown of ValueSales for Neurostimulation & Neuromodulation Devices andBiomaterials for the Years 2012, 2021 & 2027

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Global Nerve Repair and Regeneration Devices Market to Reach $12.9 Billion by 2027 - Yahoo Finance

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2023 to be highly lucrative for drug developers across therapeutic areas: Report – BSI bureau

Posted: October 13, 2022 at 2:30 am

Citeline shares insights on a longer-term outlook at some key late-stage drugs projected to hit the market in 2023

Citeline(formerly Informa Pharma Intelligence) has recently published the Key Potential Drug Launches in 2023 report sharing insights on a longer-term outlook of some key late-stage drugs projected to hit the market in 2023.

Chronic Heart Failure (CHF) remains a key area of attention for drug makers. In this scenario, Furoscix is a reformulation of the diuretic furosemide which has been developed for the treatment of decompensated heart failure and designed to be self-administered in the outpatient setting through a subcutaneous infusion via a wearable, on-body drug delivery system. Currently, the Prescription Drug User Fee Act (PDUFA) date for Furoscix is set at October 8 2022 following a resubmission of an NDA in April 2022 which included data from the Phase III FREEDOM HF trial, where the overall and heart failure-related costs of treating congestion in patients with CHF were investigated.

Simultaneously, Omecamtiv Mecarbil is another soon-to-be-launched drug, which will provide additional means of improving outcomes on top of the standard of care for those patients with more advanced stages of CHF.

In the Oncology space, for Bone Marrow Transplant and Stem Cell Transplant, Gamida Cells omidubicel is a nicotinamide (NAM)-enabled stem cell therapy being studied for use in allogeneic hematopoietic (bone marrow) stem cell transplants for patients with hematologic malignancies like acute lymphocytic leukemia.

In June 2022, Gamida Cell completed its submission to the FDA for omidubicels biologics license application, with a final decision expected in June 2023 if there are no delays.

Breyanzi has demonstrated encouraging results in the Phase I/II TRANSCEND-CLL-004 trial, reporting higher observed overall response rates compared to other investigational CD 19-directed CAR-T therapies, such as Kymriah. Breyanzi looks set to emerge as a revolutionary option for this last-line treatment setting, pending its supplemental approval in 2023.

For Haematology, Vertex had announced that global regulatory filings for exa-cel (CTX001) in transfusion-dependent beta-thalassemia (TDT) and sickle cell disease are expected by the end of 2022 which if successful, could in 2023 make it the first CRISPR/Cas 9 based product ever approved, an important boost for the gene editing technology.

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2023 to be highly lucrative for drug developers across therapeutic areas: Report - BSI bureau

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Pluristyx, panCELLa, and Implant Therapeutics Announce Definitive Merger Agreement – Business Wire

Posted: October 13, 2022 at 2:28 am

SEATTLE--(BUSINESS WIRE)--Today, Pluristyx, panCELLa, and Implant Therapeutics management are excited to announce their corporate merger, pending shareholder approval. The merged company will combine complementary portfolios to offer end-to-end customer support and provide increased access to a wide range of induced pluripotent stem cell (iPSC)-related products and services. The integrated technological and service offerings will greatly accelerate the development and delivery of revolutionary cell therapies to patients.

This merger announcement follows their successful partnership in January 2022 which enables streamlined access to the next generation of safe, universal, cost-effective, off-the-shelf" iPSCs. Pluristyx/panCELLas iPSCs are generated through a proprietary mRNA-based technology and are conveniently available in a try-before-you-buy research evaluation model requiring low up-front licensing fees. Packaged in Pluristyxs Ready-to-Differentiate format, iPSCs containing panCELLas FailSafe and hypoimmunogenic technologies offer customers, at any stage of product development, the ability to rapidly assess and select lines for further development and manufacturing. Since Plurisytx/panCELLa iPSCs are sourced from clinical-grade material, commercial partners can readily transition from development to therapeutic manufacturing.

Regarding this merger, Mahendra Rao, Co-Chairman of the Board at panCELLa and CEO of Implant Therapeutics, commented, We are extremely excited to be joining forces with Pluristyx. From the start of our collaboration, it was clear that the expertise and strong track record in cell therapy development within the Pluristyx team was the perfect fit to maximize the customer benefit from our technologies. By coming together, we can offer clients an industry-leading suite of technologies and services for the next generation of cell therapies.

Benjamin Fryer, Chief Executive Officer, Pluristyx said: In discussions with customers, it became evident that panCELLas hypoimmune and FailSafe technologies are seen as industry gold-standards. This merger takes us one step farther in our journey to become the leading provider of iPSC and cell therapy solutions for research, diagnostic, and clinical applications. Together with the expertise and technology portfolio of panCELLa, we can now provide a full suite of tools and provide the fastest path to gene-edited iPSC-based therapies.

The merged companies will retain the Pluristyx name with panCELLa becoming a wholly owned subsidiary of Pluristyx. Benjamin Fryer will continue as the Chief Executive Officer and Mahendra Rao will take on the role of Chief Science Officer. Current Pluristyx and panCELLa executives will be Jason Carstens as the Chief Operating Officer, Brian Hawkins as the Chief Technology Officer, Kaye Reiter as General Counsel, Jake Krembil as VP of Business Development/Toronto Site Lead, and James Laing as VP of Finance.

About Pluristyx

Pluristyx is a privately held biotechnology company based in Seattle, WA that offers consulting, wet-lab and GMP banking services, and pluripotent stem cell products to support novel therapeutic developers. Pluristyx helps industry and academic researchers solve manufacturing and analytical challenges in cryopreservation, drug development, regenerative medicine, and cell and gene therapy. The Pluristyx team has decades of experience supporting every stage of cell therapy product development, from cell banking to drug product manufacturing including analytical testing and release of clinical grade cell therapy products. To learn more, visit http://www.pluristyx.com or email info@pluristyx.com.

About panCELLa

Co-founded in 2015 by Dr. Andras Nagy, PhD, stem cell biologist and Dr. Armand Keating, MD, PhD, clinical scientist, and hematologist, panCELLa is a privately held early-stage biotechnology firm based on the innovative technology developed in Dr. Andras Nagys lab at the Sinai Health System (SHS) in Toronto, Canada. panCELLa has created platforms that allow for the development of safe, universal, cost-effective, off-the-shelf therapeutic cell products for medicine. panCELLa has secured partnerships with several biotechnology partners to enhance its patent position and provide expanded access to its exclusive FailSafe and Cloaked Cells/iACT cells. panCELLa continues its internal R&D efforts to develop additional novel uses of its platform technologies in areas such as bio-production, cancer vaccination and tolerization. To learn more, visit https://pancella.com.

About Implant Therapeutics

A subsidiary of panCELLa, Implant is a biotechnology company based in Maryland, United States. As a developer of genetically engineered stem cells, Implant combines the advantages of iPSC-MSC with panCELLas exclusive safety platforms to deliver the ultimate therapeutic MSC products. To learn more, visit: http://www.implant-rx.com

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Pluristyx, panCELLa, and Implant Therapeutics Announce Definitive Merger Agreement - Business Wire

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Louise Bourgeois – Wikipedia

Posted: October 13, 2022 at 2:27 am

French-American artist (19112010)

Louise Josphine Bourgeois (French:[lwiz buwa] (listen); 25 December 1911 31 May 2010)[1] was a French-American artist. Although she is best known for her large-scale sculpture and installation art, Bourgeois was also a prolific painter and printmaker. She explored a variety of themes over the course of her long career including domesticity and the family, sexuality and the body, as well as death and the unconscious.[2] These themes connect to events from her childhood which she considered to be a therapeutic process. Although Bourgeois exhibited with the Abstract Expressionists and her work has much in common with Surrealism and Feminist art, she was not formally affiliated with a particular artistic movement.

Bourgeois was born on 25 December 1911 in Paris, France.[3] She was the middle child of three born to parents Josphine Fauriaux and Louis Bourgeois.[4] Her parents owned a gallery that dealt primarily in antique tapestries. A few years after her birth, her family moved out of Paris and set up a workshop for tapestry restoration below their apartment in Choisy-le-Roi, for which Bourgeois filled in the designs where they had become worn.[3][5] The lower part of the tapestries were always damaged which was usually a result of the characters' feet and animals' paws.

In 1930, Bourgeois entered the Sorbonne to study mathematics and geometry, subjects that she valued for their stability,[6][7] saying "I got peace of mind, only through the study of rules nobody could change."[7]

Her mother died in 1932, while Bourgeois was studying mathematics. Her mother's death inspired her to abandon mathematics and to begin studying art. She continued to study art by joining classes where translators were needed for English-speaking students, especially because translators were not charged tuition. In one such class, Fernand Lger saw her work and told her she was a sculptor, not a painter.[6] Bourgeois took a job as a docent, leading tours at the Muse du Louvre.[8]

Bourgeois graduated from the Sorbonne in 1935. She began studying art in Paris, first at the cole des Beaux-Arts and cole du Louvre, and after 1932 in the independent academies of Montparnasse and Montmartre such as Acadmie Colarossi, Acadmie Ranson, Acadmie Julian, Acadmie de la Grande Chaumire and with Andr Lhote, Fernand Lger, Paul Colin and Cassandre.[9] Bourgeois had a desire for first-hand experience and frequently visited studios in Paris, learning techniques from the artists and assisting with exhibitions.[10]

In 1938, she opened her own gallery in a space next door to her father's tapestry gallery where she showed the work of artists such as Eugne Delacroix, Henri Matisse and Suzanne Valadon,[11] and where she met visiting American art professor Robert Goldwater as a customer. They married and moved to the United States (where he taught at New York University). They had three sons; one was adopted. The marriage lasted until Goldwater's death in 1973.[6]

Bourgeois settled in New York City with her husband in 1938. She continued her education at the Art Students League of New York, studying painting under Vaclav Vytlacil, and also producing sculptures and prints.[7] "The first painting had a grid: the grid is a very peaceful thing because nothing can go wrong ... everything is complete. There is no room for anxiety ... everything has a place, everything is welcome."[12]

Bourgeois incorporated those autobiographical references to her sculpture Quarantania I, on display in the Cullen Sculpture Garden at the Museum of Fine Arts, Houston.[13]

For Bourgeois, the early 1940s represented the difficulties of a transition to a new country and the struggle to enter the exhibition world of New York City. Her work during this time was constructed from junkyard scraps and driftwood which she used to carve upright wood sculptures. The impurities of the wood were then camouflaged with paint, after which nails were employed to invent holes and scratches in the endeavor to portray some emotion. The Sleeping Figure is one such example which depicts a war figure that is unable to face the real world due to vulnerability. Throughout her life, Bourgeois's work was created from revisiting her own troubled past as she found inspiration and temporary catharsis from her childhood years and the abuse she suffered from her father. Slowly she developed more artistic confidence, although her middle years are more opaque, which might be due to the fact that she received very little attention from the art world despite having her first solo show in 1945.[14] In 1951, her father died and she became an American citizen.[15]

In 1954, Bourgeois joined the American Abstract Artists Group, with several contemporaries, among them Barnett Newman and Ad Reinhardt. At this time she also befriended the artists Willem de Kooning, Mark Rothko, and Jackson Pollock.[10]As part of the American Abstract Artists Group, Bourgeois made the transition from wood and upright structures to marble, plaster, and bronze as she investigated concerns like fear, vulnerability, and loss of control. This transition was a turning point. She referred to her art as a series or sequence closely related to days and circumstances, describing her early work as the fear of falling which later transformed into the art of falling and the final evolution as the art of hanging in there. Her conflicts in real life empowered her to authenticate her experiences and struggles through a unique art form. In 1958, Bourgeois and her husband moved into a terraced house at West 20th Street, in Chelsea, Manhattan, where she lived and worked for the rest of her life.[6]

Despite the fact that she rejected the idea that her art was feminist, Bourgeois's subject was the feminine. Works such as Femme Maison (19461947), Torso self-portrait (19631964), and Arch of Hysteria (1993), all depict the feminine body. In the late 1960s, her imagery became more explicitly sexual as she explored the relationship between men and women and the emotional impact of her troubled childhood. Sexually explicit sculptures such as Janus Fleuri (1968) show she was not afraid to use the female form in new ways.[16] She stated, "My work deals with problems that are pre-gender," she wrote. "For example, jealousy is not male or female."[17] With the rise of feminism, her work found a wider audience. Despite this assertion, in 1976 Femme Maison was featured on the cover of Lucy Lippard's book From the Center: Feminist Essays on Women's Art and became an icon of the feminist art movement.[1]

In 1973, Bourgeois started teaching at the Pratt Institute, Cooper Union, Brooklyn College and the New York Studio School of Drawing, Painting and Sculpture. From 1974 until 1977, Bourgeois worked at the School of Visual Arts in New York where she taught printmaking and sculpture.[1] She also taught for many years in the public schools in Great Neck, Long Island.

In the early 1970s, Bourgeois held gatherings called "Sunday, bloody Sundays" at her home in Chelsea. These salons would be filled with young artists and students whose work would be critiqued by Bourgeois. Bourgeois's ruthlessness in critique and her dry sense of humor led to the naming of these meetings. Bourgeois inspired many young students to make art that was feminist in nature.[18] However, Louise's long-time friend and assistant, Jerry Gorovoy, has stated that Louise considered her own work "pre-gender."[19]

Bourgeois aligned herself with activists and became a member of the Fight Censorship Group, a feminist anti-censorship collective founded by fellow artist Anita Steckel. In the 1970s, the group defended the use of sexual imagery in artwork.[20] Steckel argued, "If the erect penis is not wholesome enough to go into museums, it should not be considered wholesome enough to go into women."[21]

In 1978 Bourgeois was commissioned by the General Services Administration to create Facets of the Sun, her first public sculpture.[1] The work was installed outside of a federal building in Manchester, New Hampshire.[1]Bourgeois received her first retrospective in 1982, by the Museum of Modern Art in New York City. Until then, she had been a peripheral figure in art whose work was more admired than acclaimed. In an interview with Artforum, timed to coincide with the opening of her retrospective, she revealed that the imagery in her sculptures was wholly autobiographical. She shared with the world that she obsessively relived through her art the trauma of discovering, as a child, that her English governess was also her father's mistress.[22][23]

In 1989, Bourgeois made a drypoint etching, Mud Lane, of the home she maintained in Stapleton, Staten Island, which she treated as a sculptural environment rather than a living space.[24]

Bourgeois had another retrospective in 1989 at Documenta 9 in Kassel, Germany.[14] In 1993, when the Royal Academy of Arts staged its comprehensive survey of American art in the 20th century, the organizers did not consider Bourgeois's work of significant importance to include in the survey.[22] However, this survey was criticized for many omissions, with one critic writing that "whole sections of the best American art have been wiped out" and pointing out that very few women were included.[25] In 2000 her works were selected to be shown at the opening of the Tate Modern in London.[14]In 2001, she showed at the Hermitage Museum.[26]

In 2010, the last year of her life, Bourgeois used her art to speak up for Lesbian, Gay, Bisexual and Transgender (LGBT) equality. She created the piece I Do, depicting two flowers growing from one stem, to benefit the nonprofit organization Freedom to Marry. Bourgeois has said "Everyone should have the right to marry. To make a commitment to love someone forever is a beautiful thing."[27] Bourgeois had a history of activism on behalf of LGBT equality, having created artwork for the AIDS activist organization ACT UP in 1993.[28]

Bourgeois died of heart failure on 31 May 2010, at the Beth Israel Medical Center in Manhattan.[29][30] Wendy Williams, the managing director of the Louise Bourgeois Studio, announced her death.[30] She had continued to create artwork until her death, her last pieces being finished the week before.[31]

The New York Times said that her work "shared a set of repeated themes, centered on the human body and its need for nurture and protection in a frightening world."[32]

Her husband, Robert Goldwater, died in 1973. She was survived by two sons, Alain Bourgeois and Jean-Louis Bourgeois. Her first son, Michel, died in 1990.[33]

Femme Maison (194647) is a series of paintings in which Bourgeois explores the relationship of a woman and the home. In the works, women's heads have been replaced with houses, isolating their bodies from the outside world and keeping their minds domestic. This theme goes along with the dehumanization of modern art.[34]

Destruction of the Father (1974) is a biographical and a psychological exploration of the power dominance of father and his offspring. The piece is a flesh-toned installation in a soft and womb-like room. Made of plaster, latex, wood, fabric, and red light, Destruction of the Father was the first piece in which she used soft materials on a large scale. Upon entering the installation, the viewer stands in the aftermath of a crime. Set in a stylized dining room (with the dual impact of a bedroom), the abstract blob-like children of an overbearing father have rebelled, murdered, and eaten him.[35]

... telling the captive audience how great he is, all the wonderful things he did, all the bad people he put down today. But this goes on day after day. There is tragedy in the air. Once too often he has said his piece. He is unbearably dominating although probably he does not realize it himself. A kind of resentment grows and one day my brother and I decided, 'the time has come!' We grabbed him, laid him on the table and with our knives dissected him. We took him apart and dismembered him, we cut off his penis. And he became food. We ate him up ... he was liquidated the same way he liquidated the children.[36][failed verification]

In 1982, The Museum of Modern Art in New York City featured unknown artist, Louise Bourgeois' work. She was 70 years old and a mixed media artist who worked on paper and with metal, marble and animal skeletal bones. Childhood family traumas "bred an exorcism in art", and she desperately attempted to purge her unrest through her work. She felt she could get in touch with issues of female identity, the body, and the fractured family long before the art world and society considered them as subjects to be expressed in art. This was Bourgeous' way to find her center and stabilize her emotional unrest. The New York Times said at the time that "her work is charged with tenderness and violence, acceptance and defiance, ambivalence and conviction."[37]

While in her eighties, Bourgeois produced two series of enclosed installation works she referred to as Cells. Many are small enclosures into which the viewer is prompted to peer inward at arrangements of symbolic objects; others are small rooms into which the viewer is invited to enter. In the cell pieces, Bourgeois uses earlier sculptural forms, found objects as well as personal items that carried strong personal emotional charge for the artist.

The cells enclose psychological and intellectual states, primarily feelings of fear and pain. Bourgeois stated that the Cells represent "different types of pain; physical, emotional and psychological, mental and intellectual ... Each Cell deals with a fear. Fear is pain ... Each Cell deals with the pleasure of the voyeur, the thrill of looking and being looked at."[38]

In the late 1990s, Bourgeois began using the spider as a central image in her art. Maman, which stands more than nine metres high, is a steel and marble sculpture from which an edition of six bronzes were subsequently cast. It first made an appearance as part of Bourgeois's commission for The Unilever Series for Tate Modern's Turbine Hall in 2000, and recently, the sculpture was installed at the Qatar National Convention Centre in Doha, Qatar.[39] Her largest spider sculpture titled Maman stands at over 30 feet (9.1m) and has been installed in numerous locations around the world.[40]It is the largest Spider sculpture ever made by Bourgeois.[36]Moreover, Maman alludes to the strength of her mother, with metaphors of spinning, weaving, nurture and protection.[36] The prevalence of the spider motif in her work has given rise to her nickname as Spiderwoman.[41]

The Spider is an ode to my mother. She was my best friend. Like a spider, my mother was a weaver. My family was in the business of tapestry restoration, and my mother was in charge of the workshop. Like spiders, my mother was very clever. Spiders are friendly presences that eat mosquitoes. We know that mosquitoes spread diseases and are therefore unwanted. So, spiders are helpful and protective, just like my mother.

Bourgeois's Maisons fragiles / Empty Houses sculptures are parallel, high metallic structures supporting a simple tray. One must see them in person to feel their impact. They are not threatening or protecting, but bring out the depths of anxiety within you. Bachelard's findings from psychologists' tests show that an anxious child will draw a tall narrow house with no base. Bourgeois had a rocky/traumatic childhood and this could support the reason behind why these pieces were constructed.[12]

Bourgeois's printmaking flourished during the early and late phases of her career: in the 1930s and 1940s, when she first came to New York from Paris, and then again starting in the 1980s, when her work began to receive wide recognition. Early on, she made prints at home on a small press, or at the renowned workshop Atelier 17. That period was followed by a long hiatus, as Bourgeois turned her attention fully to sculpture. It was not until she was in her seventies that she began to make prints again, encouraged first by print publishers. She set up her old press, and added a second, while also working closely with printers who came to her house to collaborate. A very active phase of printmaking followed, lasting until the artist's death. Over the course of her life, Bourgeois created approximately 1,500 printed compositions.

In 1990, Bourgeois decided to donate the complete archive of her printed work to The Museum of Modern Art. In 2013, The Museum launched the online catalogue raisonn, "Louise Bourgeois: The Complete Prints & Books." The site focuses on the artist's creative process and places Bourgeois's prints and illustrated books within the context of her overall production by including related works in other mediums that deal with the same themes and imagery.

One theme of Bourgeois's work is that of childhood trauma and hidden emotion.[42] After Louise's mother became sick with influenza Louise's father began having affairs with other women, most notably with Sadie, Louise's English tutor. He would bring mistresses back home and be unfaithful in front of his whole family.[43] Louise was extremely watchful and aware of the situation. This was the beginning of the artist's engagement with double standards related to gender and sexuality, which was expressed in much of her work. She recalls her father saying "I love you" repeatedly to her mother, despite infidelity. "He was the wolf, and she was the rational hare, forgiving and accepting him as he was."[44] Her 1993 work Cell: You Better Grow Up, part of her Cell series, speaks directly to Louise's childhood trauma and the insecurity that surrounded her. 2002's Give or Take is defined by hidden emotion, representing the intense dilemma that people face throughout their lives as they attempt to balance the actions of giving and taking. This dilemma is not only represented by the shape of the sculpture, but also the heaviness of the material this piece is made of.[original research?]

Motherhood is another recurrent theme of Bourgeois's work. It was her mother who encouraged Bourgeois to draw and who involved her in the tapestry business. Bourgeois considered her mother to be intellectual and methodical; the continued motif of the spider in her work often represents her mother. The notion of a spider that spins and weaves its web is a direct reference to her parents' tapestry business and can also be seen as a metaphor for her mother, who repairs things.[11]

Bourgeois has explored the concept of feminity through challenging the patriarchal standards and making artwork about motherhood rather than showing women as muses or ideals.[42] She has been described as the 'reluctant hero of feminist art'.[45] Louise Bourgeois had a feminist approach to her work similar to fellow artists such as Agnes Martin and Eva Hesse, less driven by the political but rather made work that drew on their experiences of gender and sexuality, naturally engaging with women's issues.[11]

Architecture and memory are important components of Bourgeois's work.[46] Bourgeois's work are very organic, biological, reproductive feel to them; they draw attention to the work itself.[43] Louise describes architecture as a visual expression of memory, or memory as a type of architecture. The memory which is featured in much of her work is an invented memory about the death or exorcism of her father. The imagined memory is interwoven with her real memories including living across from a slaughterhouse and her father's affair. To Louise her father represented injury and war, aggrandizement of himself and belittlement of others and most importantly a man who represented betrayal.[44] Her 1993 work Cell (Three White Marble Spheres) speaks to fear and captivity. The mirrors within the present an altered and distorted reality.[original research?]

Sexuality is undoubtedly one of the most important themes in the work of Louise Bourgeois. The link between sexuality and fragility or insecurity is also powerful. It has been argued that this stems from her childhood memories and her father's affairs. 1952's Spiral Woman combines Louise's focus on female sexuality and torture. The flexing leg and arm muscles indicate that the Spiral Woman is still above though she is being suffocated and hung. 1995's In and Out uses cold metal materials to link sexuality with anger and perhaps even captivity.[original research?]

The spiral in her work demonstrates the dangerous search for precarious equilibrium, accident-free permanent change, disarray, vertigo, whirlwind. There lies the simultaneously positive and negative, both future and past, breakup and return, hope and vanity, plan and memory.[original research?]

Louise Bourgeois's work is powered by confessions, self-portraits, memories, fantasies of a restless being who is seeking through her sculpture a peace and an order which were missing throughout her childhood.[12]

This collaboration took place over a span of two years with British artist Tracey Emin. The work was exhibited in London months after Bourgeois's death in 2010. The subject matter consists of male and female images. Although they appear sexual, it portrays a tiny female figure paying homage to a giant male figure, like a God. Louise Bourgeois did the water colors and Tracey Emin did the drawing on top. It took Emin two years to decide how to figure out what she would contribute in the collaboration. When she knew what to do, she finished all of the drawings in a day and believes every single one worked out perfectly. I Lost You is about losing children, losing life. Bourgeois had to bury her son as a parent. Abandonment for her is not only about losing her mother but her son as well. Despite the age gap between the two artists and differences in their work, the collaboration worked out gently and easily.[47][according to whom?]

Major holdings of her work include the following.

Throughout her career, Bourgeois knew many of her core collectors, such as Ginny Williams, Agnes Gund, Ydessa Hendeles and Ursula Hauser.[86] Other private collections with notable Bourgeois pieces include the Goetz Collection in Munich.[86]

Bourgeois started working with gallerist Paule Anglim in San Francisco in 1987, Karsten Greve in Paris in 1990, and Hauser & Wirth in 1997. Hauser & Wirth has been the principal gallery for her estate. Others, such as Kukje Gallery in Seoul and Xavier Hufkens in Brussels continue to deal in her work.[86]

In 2011 one of Bourgeois's works, titled Spider, sold for $10.7 million, a new record price for the artist at auction,[87] and the highest price paid for a work by a woman at the time.[88] In late 2015, the piece sold at another Christie's auction for $28.2 million.[89]

Louise Bourgeois in The Museum of Fine Arts, Houston: https://www.mfah.org/blogs/inside-mfah/a-confessional-sculpture-by-louise-bourgeois

Awards for Louise Bourgeois

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SciSparc Ltd. Announces Receipt of Nasdaq Minimum Bid Price Notification

Posted: October 13, 2022 at 2:26 am

TEL AVIV, Israel, Oct. 12, 2022 (GLOBE NEWSWIRE) -- SciSparc Ltd. (Nasdaq: SPRC), a specialty clinical-stage pharmaceutical company focusing on the development of therapies to treat disorders of the central nervous system (the “Company” or “SciSparc”), today announced it has received a written notice (the “Notice”) from Nasdaq Stock Market LLC (“Nasdaq”) indicating that the Company is not in compliance with the minimum bid price requirement for continued listing set forth in Nasdaq Listing Rule 5550(a)(2), which requires listed securities to maintain a minimum bid price of $1.00 per share. Under Nasdaq Listing Rule 5810(c)(3)(A), the Company has been granted a period of 180 calendar days to regain compliance with the minimum bid price requirement. The Notice has no immediate effect on the Company’s Nasdaq listing or the trading of its ordinary shares, and during the grace period, as may be extended, the Company’s ordinary shares will continue to trade on Nasdaq under the symbol “SPRC”.

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