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MilliporeSigma Opens First M Lab Collaboration Center in Europe
MilliporeSigma officially opened its new M Lab Collaboration Center in Molsheim, France. The center is MilliporeSigma's first in Europe and ninth worldwide, providing biopharmaceutical…
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Merck To Collaborate with GenScript to Accelerate Cell and Gene Therapy Industrialization in China
Merck announced the signing of a non-binding Memorandum of Understanding with Chinese biotech company GenScript for a strategic alliance focusing on plasmid and viral vector…
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FDA approves Roche’s Tecentriq in combination with chemotherapy for the initial treatment of adults…
Roche announced that the U.S. Food and Drug Administration (FDA) approved Tecentriq (atezolizumab), in combination with carboplatin and etoposide (chemotherapy), for the initial…
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Data from GARNET study indicates robust activity of dostarlimab in patients with advanced or…
TESARO, an oncology-focused business acquired by GlaxoSmithKline plc, announced the presentation of data from the Phase 1/2 GARNET study evaluating dostarlimab in women with recurrent…
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Boehringer Ingelheim announces FDA and EMA regulatory submission for nintedanib in systemic…
Boehringer Ingelheim has filed for regulatory approval of nintedanib in patients with systemic sclerosis associated interstitial lung disease (SSc-ILD) with the FDA and EMA. Nintedanib…
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Iktos Announces Collaboration with Merck for Use of Iktos AI Technology across Three Drug Discovery…
Iktos announced a collaboration agreement with Merck KGaA, Darmstadt, Germany where Iktos generative modelling artificial intelligence (AI) technology will be used to facilitate the…
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Existing drug found to dampen chemo side effects in breast cancer — in a dish
Patients with HER2-positive breast cancer face something of a predicament: The most effective drug to treat the cancer is also the most toxic.
Trastuzumab, sold under the brand name…
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European Commission approves Roche’s MabThera (rituximab) for a rare autoimmune disease
Roche announced that the European Commission has approved MabThera® (rituximab) for the treatment of adults with moderate to severe pemphigus vulgaris (PV), a rare condition…
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EC approves Roche’s Hemlibra for people with severe haemophilia A without factor VIII inhibitors
Roche announced that the European Commission has approved Hemlibra (emicizumab) for routine prophylaxis of bleeding episodes in people with severe haemophilia A (congenital factor VIII…
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Seres Therapeutics Announces Microbiome Immuno-Oncology Focused Collaboration with AstraZeneca
Seres Therapeutics announced a three-year research collaboration with AstraZeneca. The collaboration will focus on advancing mechanistic understanding of the microbiome in augmenting…
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FDA Approves Pfizer’s Oncology Biosimilar TRAZIMERA (trastuzumab-qyyp), a Biosimilar to Herceptin 1
Pfizer Inc. announced the United States (U.S.) Food and Drug Administration (FDA) has approved TRAZIMERA (trastuzumab-qyyp), a biosimilar to Herceptin (trastuzumab), for the treatment…
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Gilead Announces Data From Two Studies Supporting Further Development of GS-6207, a Novel,…
Gilead Sciences, Inc. announced findings from two studies that support the further development of GS-6207, a novel, selective, first-in-class inhibitor of HIV-1 capsid function, for…
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Lynparza significantly delayed disease progression as 1st-line maintenance treatment in germline…
AstraZeneca and MSD Inc., Kenilworth, N.J., US (MSD: known as Merck & Co., Inc. inside the US and Canada) announced positive results from the Phase III POLO trial.
Results from…
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AbbVie and Voyager Announce Collaboration to Develop Vectorized Antibodies to Treat…
AbbVie and Voyager Therapeutics announced an exclusive, global strategic collaboration and option agreement to develop and commercialize vectorized antibodies directed at pathological…
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Abbott and Novo Nordisk enter partnership to provide integrated digital solution to people with…
Abbott and Novo Nordisk announced a non-exclusive partnership that will integrate insulin dose data from Novo Nordisk pre-filled and durable connected pens directly into the digital…
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Novo Nordisk receives FDA approval of ESPEROCT (turoctocog alfa pegol, N8-GP)
Novo Nordisk announced that the US Food and Drug Administration (FDA) has approved the Biologics License Application for ESPEROCT for the treatment of adults and children with…
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Boehringer and Lilly’s CAROLINA cardiovascular outcome trial for Trajenta meets primary endpoint of…
Boehringer Ingelheim and Eli Lilly and Company announced CAROLINA (CARdiovascular Outcome study of LINAgliptin versus glimepiride in patients with type 2 diabetes) met its primary…
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Merck Increases Focus on Advanced Prostate Cancer, Expanding Immuno-Oncology Program with Three New…
Merck, known as MSD outside the United States and Canada, announced the presentation of interim data from the Phase 1b/2 KEYNOTE-365 umbrella trial investigating KEYTRUDA, Merck’s…
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Novartis receives FDA approval for Egaten for the treatment of fascioliasis, a neglected tropical…
Novartis announced that the US Food and Drug Administration (FDA) has approved Egaten (triclabendazole) for the treatment of fascioliasis in patients six years of age and older. This…
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AbbVie and Teneobio Announce a Strategic Transaction to Develop a New Treatment for Multiple Myeloma
AbbVie, Teneobio, Inc. and its affiliate TeneoOne, Inc. announced that they have entered a global strategic transaction to develop and commercialize TNB-383B, a BCMA-targeting…
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