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Category Archives: Global News Feed
Organogenesis Reports Positive Interim Analysis of Second Phase 3 Clinical Trial of ReNu for Knee Osteoarthritis
Posted: November 12, 2024 at 2:47 am
CANTON, Mass., Nov. 11, 2024 (GLOBE NEWSWIRE) -- Organogenesis Holdings Inc. (Nasdaq: ORGO), a leading regenerative medicine company focused on the development, manufacture, and commercialization of product solutions for the Advanced Wound Care and Surgical and Sports Medicine markets, today announced the favorable outcome of the interim analysis of its second Phase 3 randomized control trial of ReNu, a cryopreserved amniotic suspension allograft (ASA), for the management of symptoms associated with knee osteoarthritis (OA).
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23andMe Announces Business Restructuring to Streamline Operations, Reduce Costs and Position Company for the Future
Posted: November 12, 2024 at 2:47 am
Reduces workforce by roughly 40%; expects annualized cost savings of more than $35 million
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23andMe Announces Business Restructuring to Streamline Operations, Reduce Costs and Position Company for the Future
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MediciNova Given Notice of Monetary Damages Due Under Patent Settlement of Sanofi-Novartis
Posted: November 12, 2024 at 2:47 am
LA JOLLA, Calif., Nov. 11, 2024 (GLOBE NEWSWIRE) -- MediciNova, Inc., a biopharmaceutical company traded on the NASDAQ Global Market (NASDAQ: MNOV) and the Standard Market of the Tokyo Stock Exchange (Code Number: 4875), today announced that it was notified by Sanofi that the Sanofi/Novartis litigation was settled. Accordingly, MediciNova is entitled to receive a certain amount of monetary damages through this settlement. Further details will be provided as they become available.
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MediciNova Given Notice of Monetary Damages Due Under Patent Settlement of Sanofi-Novartis
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Santhera Enters into Exclusive Supply Agreement for AGAMREE® (Vamorolone) with Ali Al Suwaidi Trading Establishment (ASTE) in Qatar
Posted: November 12, 2024 at 2:47 am
Pratteln, Switzerland, November 12, 2024 – Santhera Pharmaceuticals (SIX: SANN) announces the signing of an exclusive supply agreement with Ali Al Suwaidi Trading Est. (ASTE) for the treatment of patients with Duchenne muscular dystrophy (DMD) with AGAMREE under a Named Patient Program.
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Belite Bio Reports Third Quarter 2024 Financial Results and Provides a Corporate Update
Posted: November 12, 2024 at 2:47 am
SAN DIEGO, Nov. 12, 2024 (GLOBE NEWSWIRE) -- Belite Bio, Inc (NASDAQ: BLTE) (“Belite” or the “Company”), a clinical-stage biopharmaceutical drug development company focused on advancing novel therapeutics targeting degenerative retinal diseases that have significant unmet medical needs, today announced its financial results for the third quarter ended September 30, 2024, and provided a general business update.
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Belite Bio Reports Third Quarter 2024 Financial Results and Provides a Corporate Update
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Valneva to Present and Hold Investor Meetings at Upcoming U.S. and European Healthcare Conferences
Posted: November 12, 2024 at 2:47 am
Saint-Herblain (France), November 12, 2024 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announced that its senior management will present and participate in 1-on-1 meetings with institutional investors at upcoming investor conferences in the United States and Europe.
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Valneva to Present and Hold Investor Meetings at Upcoming U.S. and European Healthcare Conferences
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NANOBIOTIX Provides Third Quarter 2024 Update and Progress on Nanotherapeutics Platforms
Posted: November 12, 2024 at 2:47 am
PARIS and CAMBRIDGE, Mass., Nov. 12, 2024 (GLOBE NEWSWIRE) -- NANOBIOTIX (Euronext: NANO - NASDAQ: NBTX - the “Company”), a late-clinical stage biotechnology company pioneering nanoparticle-based approaches to expand treatment possibilities for patients with cancer and other major diseases, provided an update on operational progress and reported financial results for the third quarter of 2024.
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NANOBIOTIX Provides Third Quarter 2024 Update and Progress on Nanotherapeutics Platforms
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Novartis Scemblix® FDA approved in newly diagnosed CML, offering superior efficacy, and favorable safety and tolerability profile
Posted: October 30, 2024 at 2:42 am
Ad hoc announcement pursuant to Art. 53 LR
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Novartis Scemblix® FDA approved in newly diagnosed CML, offering superior efficacy, and favorable safety and tolerability profile
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Cognition Therapeutics Announces Results of Pre-specified Analysis of SHINE Study Data Presented at CTAD
Posted: October 30, 2024 at 2:42 am
- Results show CT1812 dramatically slowed cognitive decline in patients with lower levels of plasma p-tau217, an important biomarker of Alzheimer’s disease pathology -
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