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Advancements in Biotechnology to Boost Uptake of Ampoules Worldwide – TMR Research Blog (press release) (blog)

Posted: June 20, 2017 at 6:45 pm

San Francisco, California, June 20, 2017: The flourishing growth of the pharmaceutical packaging industry worldwide is the primary growth stimulant of the global ampoules market worldwide. The advent of novel injectable therapies due to research and advancements in the field of biotechnology is also augmenting the market. A report by TMR Research, titled Ampoules Market Global Industry Analysis, Size, Share, Trends, Analysis, Growth, and Forecast 20172025, extensively covers all the vital parameters of the market, including vendor landscape and regional segmentation.

Stringent government regulatory framework and industry standards for pharmaceutical packaging are stoking the growth of the global ampoules market. Strict standards and regulations are compelling manufacturers to elevate their packaging practices such that there is no compromise in terms of efficacy and quality of drugs. The spiraling demand for safer transportation of reactive liquids is also providing a significant push to the global market. Besides this, the increasing usage of ampoules in the food and beverage industry is working in favor of the global market.

On the flip side, dumping of ampoules still remains a major concern among governments and pharmaceutical organizations worldwide. Plastics and glasses are non-degradable and therefore, have impact the environment negatively. The rising environmental concerns are, thus, limiting the market from realizing its utmost potential. Nevertheless, the rising incorporation of sustainable materials such as biodegradable plastics or green plastics in the manufacturing of ampoules is likely to provide a significant momentum to the market in the near future. Furthermore, market participants are increasingly focusing towards product extensions and technological innovations, which is expected to bode well for the growth of the market.

On the basis of geography, the market can be fragmented into Europe, Latin America, North America, Asia Pacific, and the Middle East and Africa. North America and Europe are anticipated to account for a substantial cumulative share in the global ampoules market. Rapid advancements in the biotechnology in these regions are augmenting the applications of ampoules. While developed countries will be major revenue contributors, developing regions will emerge as a strong contender during the review period. Asia Pacific is estimated to witness healthy growth, owing to the robust growth of the pharmaceutical and packaging industry.

Some of the key companies operating in the global market for ampoules are Truking Technology Limited, Bausch-Stroebel, Hunan China Sun Pharmaceutical Machinery Co. Ltd., Shanghai Far-East Pharmaceutical Machinery CO. Ltd., Nipro Glass, SCHOTT, Gujarat Fabricators, Essco Glass, Kishore Group, Ciron Group of Companies, James Alexander Corporation, Kapoor Glass Pvt. Ltd, A. H. Industries, Global Pharmatech, Claris Lifesciences Ltd., and Lifespan Biotech Private Ltd.

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3D Cell Culture Tech Advances Medical Research and Treatments – GlobeNewswire (press release)

Posted: June 20, 2017 at 6:45 pm

June 20, 2017 05:00 ET | Source: BCC Research

Wellesley, Mass., June 20, 2017 (GLOBE NEWSWIRE) --

Fast-moving developments in 3D cell culture tools and technology are accelerating cancer research and clinical applications, along with other medical research and safety applications. A new report by BCC Research forecasts that some segments could see CAGR as high as 44% in products for pharmaceuticals development through 2021. In another example, neurological safety testing could grow from a $5 million segment in 2015 to $95 million by 2021, according to 3D Cell Cultures: Technologies and Global Markets.

New cell culture products and applications are proliferating even faster than a prior BCC Research report predicted in 2015. Companies such as ThermoFisher, GEHealthcare, MerckMillipore and a range of start-ups and spinouts are pursuing diverse market segments, from cosmetics and skin care to cardiac toxicology and metabolic reactions to new drugs. The new 3D technology allows for groundbreaking visibility into tissue and cancer behaviors in the body, compared with animal testing or more general, 2D in vitro technologies.

Bioreactors with microcarriers are another 3D application seeing rapid market growth. Skin and artificial skin substitutes have been in use for years. Now some of the knowledge behind those advancements are being applied to internal medicine from liver function and metabolic disease and other adjacent fields. These new applications promise not only improved medical safety in determining dosages and tailoring treatments to a patients condition and situation, but also breakthroughs in basic research, drug discovery and development.

Research Highlights

"The standards and best practices emerging in precision cancer care, and the new findings in CNS research could certainly speed up patient-centric care. Some call it personalized medicine, or precision medicine, and it really is a revolution compared with developing mass-market drugs. We are already seeing stem cells and other tools having an impact thanks to 3D Cell Culture technology, says Robert G. Hunter, senior healthcare editor at BCC Research.

About BCC Research

BCC Research is a publisher of market research reports that provide organizations with intelligence to drive smart business decisions. By partnering with industry experts worldwide, BCC Research provides unbiased measurements and assessments of global markets covering major industrial and technology sectors, including emerging markets. For more information, please visit bccresearch.com. Follow BCC Research on Twitter at @BCCResearch.

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3D Cell Culture Tech Advances Medical Research and Treatments - GlobeNewswire (press release)

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Cell Medica Acquires Catapult Therapy for Lead WT1-TCR T-Cell Therapy – Genetic Engineering & Biotechnology News (blog)

Posted: June 20, 2017 at 6:45 pm

Cell Medica is buying Catapult Therapy TCR and the firm's gene-modified WT1-TCR (Wilms' tumor 1 proteinT-cell receptor) T-cell therapy candidate. The treatment is currently in Phase I/II development for the potential treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS).

Catapult Therapy TCR is a special purpose vehicle established by The Cell and Gene Therapy Catapult (CGT Catapult), UCL Business (UCLB), and Imperial lnnovations to develop the WT1-TCR T-cell therapy, which was originally discovered by researchers at University College London (UCL) and Imperial College London. Financial details of the acquisition were not disclosed.

Cell Medical says it plans to apply its Dominant TCR platform to generate a more effective WT1-TCR product that could also feasibly be used to treat challenging solid tumors, including mesothelioma and ovarian cancer. The firm acquired the Dominant TCR technology from UCLB in 2016.

London, U.K.-based Cell Medica and CGT Catapult will carry out further development of the next generation of T cells, and manufacturing process, at the latters recently built large-scale cell and gene therapy manufacturing center at the Stevenage BioScience Catalyst, U.K.A Phase I/II study with the enhanced Dominant WT1-TCR candidate is projected to start during late 2018.

The acquisition of the WT1-TCR cell therapy leverages the investment we made in 2016 for exclusive rights to the Dominant TCR technology, said Gregg Sando, CEO of Cell Medica. Our objective is to show how we can enhance any existing TCR cell therapy with the Dominant TCR technology to create a more effective treatment for patients with solid tumors who otherwise have a very poor prognosis. We are also looking forward to an important collaboration with CGT Catapult to initiate manufacturing at the Stevenage GMP facility, where we will work together on scale-up strategies for commercial production.

With support from Innovate UK, CGT Catapult operates as a Centre of Excellence for Innovation to help drive growth of the U.K.s cell and gene therapy industry and translate early-stage research into new therapies. "We are pleased that Cell Medica has acquired the WT1 T-cell immunotherapy," added Keith Thompson, CEO at CGT Catapult. "With their complementary technologies, they will take over the development of this exciting new therapy. The next-generation product developed in our manufacturing center underlines our ability to support the localization of cell manufacturing processes in the U.K.

Cell Medica is exploiting its proprietary activated T-cell chimeric antigen receptor (CAR) and engineered TCR platforms to develop cellular immunotherapies targeting cancer. Lead product CMD-003 (baltaleucel-T) is being evaluated in the Phase II CITADEL study as a treatment for advanced lymphomas associated with the oncogenic Epstein-Barr virus.In March, Cell Medica raised 60 million (approximately $76 million) in a Series C investment roundto support development of its pipeline.

The firm has an ongoing CAR development partnership with Baylor College of Medicine and is working with UCL to leverage the Dominant TCR technology. Cell Medicas acquisition of Delenex Therapeutics in mid-2016 gave the firm an antibody fragment platform for use in developing anticancer CAR-NKT (natural killer T cells) products, and additional immune cell engineering expertise.

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He broke ground in stem-cell research. Now he’s running for Congress. – Washington Post

Posted: June 20, 2017 at 6:45 pm

The small pack of scientists running for political office has grown by one.

Stem-cell researcher Hans Keirstead, 50, announced last week that he will try to unseat Californias Rep. Dana Rohrabacher (R). Keirstead, a Democrat with a PhD in neuroscience from the University of British Columbia, was a professor at the University of California at Irvinebefore launching and selling several biotech companies.

Rohrabacher, who represents the 48th District in Southern California, has been in Congress since 1988. Democrats there see 2018 asa vulnerable year for the incumbent. Although Republicans outnumber Democrats in thedistrict, Hillary Clinton swung it in the 2016 election. And Rohrabacher has come under scrutiny for his support of acloser relationship with Russia. In May, the chair of Orange County Democrats toldThe Washington Post that challengers were coming out the woodwork to oppose him. Five candidatesbesides Keirstead have declared they are running for the seat.

Keirstead emerged from academic and entrepreneurial fields. Hepioneered a technique to purify stem cells You cant go putting toenails into the spinal cord, he said and applied this method to spinal-cord injuries and diseases such ascancer and amyotrophic lateral sclerosis, or ALS. In 2014,he sold a stem-cell company in a deal reportedly worth more than $100 million. (He will not fundhis own campaign, he told the Los Angeles Times.) Keirstead has thesupportof314 Action, a nonprofit group that encourages scientists to seek public office.

The Post spoke by phone with the first-time candidate. The following is lightly edited for space and clarity.

TWP: Your opponent, who is a member of the House Science Committee, told Science magazine in 2012 that he loved science. How would you compare your approaches to science?

Keirstead:Im delighted that Dana Rohrabacher loves science. Thats fabulous. But Im also very convinced that he doesnt understand science. Theres a real big difference. If you love science, thats one thing. If you dont understand it, you cant effect change, and you make wrong decisions.

Dana Rohrabacher does not understand global warming. He actually attributed it to the flatulence of dinosaurs, in a serious manner, a while back. [Rohrabacher hassaid this wasa joketo make fun of scientists who study cow methane.]

His inaction and lack of understanding has tremendous detriment on the scientific community. Likewise is the funding to health care and how to fix the health-care system that [former president Barack] Obama put in place. That was not a perfect system by any means; its got problems.But it has also bettered our system. It needs to be worked with in order to further better our system.

TWP: Has your career in stem-cell research influenced your politics?

Keirstead:I was front and center in the national and international debate on stem cells. I was the first scientist in the world to have developed a treatment for spinal-cord injury using stem cells. The dramatic nature of the recovery we saw in rodents, going from paralyzed to walking, drew a great deal of attention and really put me at the center of this issue as it was just coming to light in the public forums.

I did a lot of advising of senators and congressmen all throughout those years and periodically since that time. . . . I was one of the key scientific advisers to Proposition 71 that turned into the $3 billion California Institute of Regenerative Medicine, a not-for-profit that distributes $300 million every year for regenerative medicine in a broad sense.

That was a very good example of how medical breakthroughs and discoveries and advancement are not at odds with economic development. You do not have to cut medical budgets to stimulate the economy. Any scientist and medical doctor will tell you: Give me some time, and I will generate a treatment. And most of the time they are right. What happens with that treatment is small companies are born, people stop dying, quality of life improves.

I see what the governments doing right now as very much opposite that. Frankly, when I look at the deficits of Congress, I see why. When I look at who is in the administration, the types of individuals that we have in Congress, I see very hard-working people doing what they feel is a terrific job. But there is just not the broad and deep field experience in the medical and health-care sectors.

TWP: Was it this perceived deficit that motivated you to run for Congress?

Keirstead:First and foremost, I see it as a continuation of my lifelong pursuits of trying to help people.

I see Congress as a larger stage to effect positive change. If I could have some positive influence in Congress, I could aid [those] that are trying to do good in the world but are having difficulty.

Let me give you an example: Im now expanding into brain cancer. Im running a Phase 2clinical trial with my team.I will not be able to do that if these policy changes of Trumps are instituted and a small company like mine is faced with double user fees. Its not in the budget. I cant ask an investor for another half of a million dollars for an administrative fee.

I see the administration putting insurmountable challenges in front of small businesses. Im about generating treatments to help people, putting medicines in peoples homes. And Im looking to the future and seeing that tap shut off.

Read more:

As scientists erupt in protest, a volcanologist runs for Congress

This group wants to fight anti-science rhetoric by getting scientists to run for office

Tens of thousands marched for science. Now what?

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Cell Medica buys clinical-phase WT1-TCR cell therapy – FierceBiotech

Posted: June 20, 2017 at 6:44 pm

Cell Medica has bought Catapult Therapy TCR for its clinical-phase WT1 T-cell receptor (TCR) cell therapy. Catapult Therapy TCR developed the therapy as a treatment for blood cancers, but Cell Medica thinks it can retool it to take out solid tumors.

Production of the cell therapy entails modifying a patients own T cells to identify and destroy cells that express the WT1 protein, which is associated with mesothelioma and ovarian cancer. But early development of the WT1-TCR cell therapy has eschewed these solid tumors in favor of going after acute myeloid leukemia and myelodysplastic syndrome.

That is set to change under the ownership of Cell Medica. The British biotech plans to apply the Dominant TCR technology it licensed from UCL last year to the cell therapy to equip it to treat solid tumors. The technology is designed to increase the efficacy of engineered T cells by dialing up the expression of TCRs.

Our objective is to show how we can enhance any existing TCR cell therapy with the Dominant TCR technology to create a more effective treatment for patients with solid tumors who otherwise have a very poor prognosis, Cell Medica CEO Gregg Sando said in a statement.

Cell Medica plans to work on the therapy over the next year or so with a view to starting a phase 1/2 trial late in 2018. Catapult Therapy TCR has already tested the cell therapy in a small number of patients. But those studies looked at the unenhanced version of the candidate in blood cancers.

The earlier trials were sponsored by the Cell and Gene Therapy Catapult, which set up Catapult Therapy TCR in collaboration with UCL Business and Imperial Innovationsnow called Touchstone Innovationsin 2014. CGT Catapult committed 10 million to the subsidiary. Financial details of the takeover by Cell Medica werent disclosed.

CGT Catapult will remain involved in advancing the cell therapy. Cell Medica is setting up a cell therapy manufacturing operation at CGT Catapults site in Stevenage. That operation will produce the WT1-TCR cell therapy and potentially other candidates. Cell Medica plans to transfer the WT1-TCR cell therapy to the site over the next 12 months while working with CGT Catapult to develop a commercial-scale production process.

The agreement continues a busy period for Cell Medica. Over the past 12 months the biotech has built out its technology base through the UCL licensing pact, agreements with Baylor College of Medicine and the acquisition of Delenex Therapeutics. Cell Medica followed up on these deals by raising 60 million to expand its clinical-phase pipeline.

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Apollo Hospitals bring innovative cell therapy to treat joint pain … – Hindustan Times

Posted: June 20, 2017 at 6:44 pm

Making uses of the advances in cell therapy, Apollo Hospitals on Tuesday announced partnership with RMS REGROW, to offer new regenerative medicine cell therapy products that will be a boon for patients suffering from bone and cartilage damage.

The two products- Ossron and Chondron, will address unmet clinical needs in the orthopaedic market with respect to sports injuries, accidents and alternate to hip replacements and knee replacements for a young arthritic knee.

In an exclusive tie up between Apollo Hospitals and RMS Regrow, the treatment therapy will be made available across all Apollo Hospitals, Apollo Spectra Hospitals and Apollo clinics in India.

Through several clinical trials and evaluation studies that spanned around 8 years, the company has achieved the market authorization for the two cell therapy products.

Doctors will be trained in using the products by conducting live surgical workshops and conferences etc. both nationally and internationally.

Apollo Group wants to encourage research and innovation within India for the people of India. Our association with RMS Regrow is a step to inspire talent in India to further the advancement in developing innovative healthcare treatments to reduce the growing disease burden in India, said Dr Prathap C Reddy, founder-chairman, Apollo Hospitals.

Yash Sanghavi, founder and CEO- RMS REGROW, said, It has taken 8 years of dedicated effort and innovative research to develop the two revolutionary products that will change the modalities for bone and cartilage treatment in India.

Since last 70 years, only a handful of New Chemical Entities (NCE) have been developed in India, which demonstrates a dearth of innovator drugs and new medical technologies to address a large market of bone and joint disorders.

In India, more than 15 lakh orthopaedic procedures are performed each year and Regenerative Cell Therapy is a revolutionary treatment methodology which has immense potential to liberate consumers from Joint pain.

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Swedish Biotech publishes Long-Term Data on a Dendritic Cell Therapy for Cancer – Labiotech.eu (blog)

Posted: June 20, 2017 at 6:44 pm

Immunicum has reported new data on long-term follow-up of patients treated with ilixadencel, a unique dendritic cell therapy against cancer.

Immunicum is a Swedish biotech developing a cell-based therapy against cancer. The company has just published detailed results of aPhase I/II trial evaluating its lead candidate ilixadencel, which is currently in Phase II to treat metastatic renal cell carcinoma (mRCC),for which no effective treatments are available.

The experimental therapy was administered in combination with Pfizers sunitinib, approved for the treatment of RCC, and Immunicum has kept monitoring the 11 patients after officially completing the study in 2014. As of 2017, five patients are still alive and the mean overall survival has reached 48 months, which is a huge improvement when compared to the approximately 15 months expected with standard therapies.

CT scans of the brain of a patient that showed a complete disappearance of all brain and liver metastases (a) before and (b) 6 months aftercompleting the treatment

Ilixadencel, previously known as Intuvax, is composed ofactivated dendritic cellsderived from healthy donors that are injected into the tumor, where theyrecruit the patients own immune system. Its an off-the-shelf cell therapyobtained from healthy donors, which would result in easier manufacturing and lower costs as compared to patient-derived cells.

In theory, this strategy could be applied toany injectable solid tumor,whichis particularly exciting given that targetingsolid tumors is still a huge challenge. We believe that the future of cancer treatment lies in the rapidly evolving landscape of combination therapies and ilixadencel is uniquely positioned to become an integral part of modern combination regimens, saidAlex Karlsson-Parra, CSO of Immunicum, in a statement.

According to Carlos de Sousa, CEO of the company, the effort to publish the results is part of the companys strategy to communicate its data and build validation for its technology. As he commented during an oncology panel at Labiotech Refresh, the regulatory authorities in Europe are struggling to keep up with the rapid advances in the field.

Immunicum is not the only developing cell-based therapies for cancer. The French PDC*line Pharma is also focusing on dendritic cells, while many others compete to bring the promising CAR-T cell technology to the market.Ensuring the data is available is a great initiative to help build laws that will adequately regulate these novel technologies.

Images via xrender / Shutterstock;Laurell et al., Journal for ImmunoTherapy of Cancer 2017 5:52

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This Infographic Is Like the 10 Commandments of Diabetes – Reader’s Digest

Posted: June 20, 2017 at 6:43 pm

Science is increasingly uncovering new ways toreversediabetes, achronic condition that affects the way the body processes blood sugar, and which has more than doubled in prevalence over the past 20 years, according to the Centers for Disease Control and Prevention. Scientists arealso increasingly aware of whos most at risk for the disease: According to a new study looking at the demographics of diabetes in this country, the highest risk can be found among racial and ethnic minorities, people with low incomes or lower educational levels, and people living in rural areas. In one scary finding, the research, which was published in theInternational Journal of Environmental Research and Public Health,showedthat across the country, women with diabetes were at a higher risk of foregoing medical care.

Ifyoure among the more than 29 million Americans or8.5percent of the global population withthe disease, you absolutely can live a healthy, happy lifeif you take care of yourself and follow certain diabetes guidelines.

Whether youve just been diagnosed or have been managing the disease your whole life, this handy infographic from Vitality spells out the absolute must-dos for optimum diabetes care. Follow it exactly tominimizediabetes complications and achieveyour best quality oflife. And dont miss these simple tricks for living well with diabetesfrom people who have it.

Courtesy Tips for Living Well from Vitality

Source:Tips for Living Well from Vitality

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This Infographic Is Like the 10 Commandments of Diabetes - Reader's Digest

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Sansum Diabetes Program Takes Global Stage – Noozhawk

Posted: June 20, 2017 at 6:43 pm

Posted on June 20, 2017 | 10:43 a.m.

Ocho Pasos program targets nutrition, treatment, exercise, monitoring, stress management

Jenifer Swartzentruber, l, Wendy Bevier, Mary Conneely, Ellen Goodstein of William Sansum Diabetes Center. (William Sansum Diabetes Center)

The William Sansum Diabetes Center'sOcho Pasos a la Buena Salud (Eight Steps to Better Health) was selected to be showcased in a moderated poster discussion at the recent American Diabetes Associations 77th Scientific Sessions in San Diego.

The presentation, led by WSDC diabetes educator Mary Conneely, was part of the ADA tour titled Community Strategies to Improve Care Delivery.

More than 15,000 physicians, scientists and health care professionals from around the world convene annually at the ADAs Scientific Sessions to unveil cutting-edge research, treatment recommendations and advances toward a cure for diabetes.

It was a great experience for me personally and it was just overwhelming with how much information there was at the conference, said Conneely who attended the conference for the first time this year.

During the conference Conneely said she experienced an impressive example of just how far reaching WSDCs Ocho Pasos education is across the globe.

Conneely, who is from Bolivia, met two conference attendees, also from Bolivia. When she told them about the WSDCs presentation they said they'd already downloaded WSDCs Ocho Pasos program, even before they met Conneely that day.

More than anything, it was so amazing to show other people what we are doing at William Sansum Diabetes Center and what works to better the lives of the community, Conneely said.

The moderated poster presentation detailed how Ocho Pasos is a culturally-relevant diabetes education program designed for low-income, monolingual Latino participants with or at risk for type 2 diabetes.

The eight weekly sessions focus on nutrition, treatment, monitoring, exercise and stress management. The results of Ocho Pasos were on display, highlighting the dramatic A1C reduction by taking the class.

It is incredibly empowering, energizing and awe inspiring to be around the nearly 15,000 talented and dedicated physicians, researchers, engineers, educators and others all making incredible progress in the fight against this dreadful disease," said Ellen Goodstein, WSDC executive director.

"To hear the progress being made in so many areas of diabetes research gave me genuine hope for the future. We will beat this disease, she said.

Dr. David Kerr, who attended the event, said, "The ADA showcases the best and the brightest for diabetes research and innovation, and this year the center was especially prominent because of the cutting-edge work we are involved with right now."

Diabetes affects nearly 30 million children and adults in the United States and contributes to the deaths of more than 230,000 Americans each year.

The American Diabetes Association estimates the total cost of diagnosed diabetes in the U.S. is more than $177 billion.

Published studies suggest that when additional costs for gestational diabetes, prediabetes and undiagnosed diabetes are included, the total diabetes-related costs in the U.S. exceeds $322 billion annually.

William Sansum Diabetes Center attendees included: Goodstein, Conneely, Ceara Axelrod, Wendy Bevier, Jenifer Swartzentruber, Kerr, Dr. Jordan Pinsker, Laura Lindsey and Mei Mei Church.

Regina Ruiz for William Sansum Diabetes Center.

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For diabetes drugs, lowering blood sugar may no longer be enough to stay competitive – Medical Marketing and Media

Posted: June 20, 2017 at 6:43 pm

June 19, 2017

An FDA advisory committee will meet today to discuss the results of an outcomes trial for Novo Nordisk's Victoza, an add-on treatment for diabetes, and whether the drug's label should include that it reduces the risk of death from heart attack and stroke.

The agency's meeting is part of a larger trend in diabetes, in which drugmakers are working to demonstrate that their drugs can reduce, or at least not raise, the risk of cardiovascular disease, which affects a disproportionate amount of diabetes patients. Lowering blood sugar is no longer enough.

The case for the health system is clear: adults with diabetes are twice as likely to die from heart attack or stroke compared to those without, according to the Centers for Disease Control and Prevention.

See also:BI and Lilly face a new challenge: how to market a diabetes drug to cardiologists

Drugmakers' pursuit of labels touting positive outcomes is unsurprising, given the shift towards outcomes-based contracts between drugmakers and health plans. A recent study from Avalere Health found that one in four health plans now have at least one outcomes-based contract with a drugmaker. Under these agreements, drugmakers are often paid based on the quality of care received from a product rather than its mere use.

The FDA will convene to discuss if the results from Victoza's LEADER trial change the risk-benefit profile of the drug, whether the data establish that Victoza does not increase the risk of cardiovascular disease, and if the drug proved that it reduces the risk of a heart attack or stroke in patients with existing cardiovascular disease. The trial's results were initially reported last year, revealing that Victoza cut the risk of those cardiovascular events by 13% versus placebo. Novo Nordisk filed an application in October to include the data on Victoza's label.

Positive outcomes data is not just a requirement for GLP-1 agonists like Victoza, either. At the American Diabetes Association's annual meeting last week, drugmakers unveiled new outcomes data for SGLT-2 inhibitors Farxiga (AstraZeneca) and Invokana (Johnson & Johnson).

See also:When it comes to diabetes, will marketers break with tradition?

J&J's Invokana showed the exact same benefit 14% fewer patients saw a heart attack or stroke compared to placebo in its CANVAS trial compared to fellow SGLT-2 inhibitor, Eli Lilly's Jardiance. That result should boost the entire SGLT-2 class, Credit Suisse analyst Vamil Divan wrote in an investor note. That boost, though, will likely come at Merck's expense, he added, explaining that the new data may entice doctors to use SGLT-2 inhibitors earlier in treatment and displace Merck's DPP-4 inhibitor, Januvia.

We expect the enthusiastic response to the efficacy data driving use of the SGLT-2 class earlier in the course of treatment, while concurrently pushing the DPP-4's further back, Divan wrote.

Nonetheless, Lilly's Jardiance may be the big winner in any overall boost to the SGLT-2 class due to Invokana's safety issues. The FDA slapped Invokana with a box warning in May for an increased risk of foot and leg amputations. Jardiance also has a leg up in terms of timing: last December, it became the first diabetes drug approved by the FDA to reduce cardiovascular death.

See also:Two new therapies made by Sanofi and Novo Nordisk to compete in crowded diabetes market

Invokana saw sales of $284 million in the first three months of 2017, a 12% drop from the year-ago period. Jardiance generated sales of $74 million during the same three-month period.

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