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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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UCB and Epilepsy Society announce pioneering UK Genomics R&D collaboration
The Epilepsy Society and UCB, a global biopharmaceutical company headquartered in Belgium, with a significant UK R&D hub in Slough, UK, have announced an exciting new collaboration…
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GSK signs $4.2bn immunotherapy deal with the Merck group
GlaxoSmithKline plc and Merck KGaA, Darmstadt, Germany announced that they have entered into a global strategic alliance to jointly develop and commercialise M7824 (bintrafusp alfa).…
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FDA grants Breakthrough Therapy Designation for potential next-generation RSV medicine MEDI8897
AstraZeneca and its global biologics research and development arm, MedImmune, announced that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD)…
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BioNTech to Acquire Antibody Generation Unit of MAB Discovery
BioNTech AG, a rapidly growing biotechnology company developing precise and individualized immunotherapies for the treatment of cancer and the prevention of infectious diseases, and MAB…
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FDA advisory committee votes on Zynquista (sotagliflozin) as treatment for adults with type 1…
The Endocrinologic and Metabolic Drugs Advisory Committee of the U.S. Food and Drug Administration (FDA) today voted eight to eight on the question of whether the overall benefits of…
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SCHOTT to invest 300 million euros in pharmaceutical packaging business
The SCHOTT technology group is set to invest around 300 million euros in the next three years in the expansion of its core business of glass tubing as the starting material for…
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Phoenix Molecular Designs Announces Collaboration To Develop Diagnostic for Triple-Negative Breast…
Phoenix Molecular Designs announced that it has entered into a collaboration with Roche to develop a diagnostic (CDx) in triple-negative breast cancer (TNBC). The Roche CDx identifies…
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