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Daiichi Sankyo and Merck Enter into Global Development and Commercialization Agreement for MK-6070

Aug 7, 2024
Daiichi Sankyo and Merck, known as MSD outside of the United States and Canada, have expanded their existing global co-development and co-commercialization agreement for three…
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Servier’s VORANIGO (vorasidenib) Tablets Receives FDA Approval as First Targeted Therapy for…

Aug 7, 2024
Servier announced that the U.S. Food and Drug Administration (FDA) has approved VORANIGO, an isocitrate dehydrogenase-1 (IDH1) and isocitrate dehydrogenase-2 (IDH2) inhibitor, indicated…
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Sangamo Therapeutics Announces Global Epigenetic Regulation and Capsid Delivery License Agreement…

Aug 7, 2024
Sangamo Therapeutics, Inc., a genomic medicine company, announced it has entered into a license agreement with Genentech, a member of the Roche Group, to develop intravenously…
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SK pharmteco and Rznomics Explore Collaboration for RNA-based Gene Therapy Development and…

Aug 6, 2024
SK pharmteco, a global contract development, manufacturing, and analytical testing organization serving both the small molecule and cell & gene therapy industry, and Rznomics Inc.,…
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European Commission approves Roche’s Vabysmo for treatment of retinal vein occlusion (RVO)

Jul 30, 2024
Roche announced that the European Commission (EC) has approved Vabysmo (faricimab) for the treatment of visual impairment due to macular edema secondary to retinal vein occlusion (RVO,…
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Roche closes acquisition of LumiraDx’s Point of Care technology to expand access to diagnostic…

Jul 30, 2024
Roche announced the completion of the acquisition of LumiraDx’s Point of Care technology, following the receipt of all required antitrust and regulatory clearances. Roche will now…
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Boehringer Ingelheim secures novel immune checkpoint inhibitor with acquisition of Nerio…

Jul 29, 2024
Today marks a significant step for Boehringer Ingelheim’s immuno-oncology pipeline as the company is adding an innovative preclinical program with the acquisition of Nerio…
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Novartis Scemblix granted FDA Priority Review for the treatment of adults with newly diagnosed CML

Jul 29, 2024
Novartis announced that Scemblix (asciminib) has been granted Priority Review status by the US Food and Drug Administration (FDA) for treatment of newly diagnosed adult patients with…
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Sandoz launches biosimilar Pyzchiva (ustekinumab) across Europe, to treat chronic inflammatory…

Jul 26, 2024
Sandoz, the global leader in generic and biosimilar medicines, announces the launch of Pyzchiva®* (ustekinumab) across Europe, starting today. Pyzchiva®, developed and registered by…
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AC Immune’s ACI-35.030 (now “JNJ-2056”) Granted FDA Fast Track Designation for Alzheimer’s Disease

Jul 26, 2024
AC Immune SA, a clinical-stage biopharmaceutical company pioneering precision medicine for neurodegenerative diseases, announced that its active-immunotherapy candidate, ACI-35.030 (now…
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