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Novartis Reports Positive Phase III Results for Remibrutinib in MS

Sep 3, 2026
Novartis has reported positive topline results from its Phase III REMODEL-1 and REMODEL-2 trials evaluating remibrutinib in adults with relapsing multiple sclerosis (RMS). The oral…
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Biocytogen Licenses VHH Antibody to Qilu for Neuroscience Research

Sep 3, 2026
Biocytogen Pharmaceuticals has entered into a non-exclusive licensing agreement with Qilu Pharmaceutical to support the research and development of a fully human VHH antibody for…
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Typewriter Therapeutics Launches With $56 Million Series A

Sep 3, 2026
Typewriter Therapeutics has emerged from stealth with $56 million in Series A financing to develop genetic medicines for cancer, autoimmune diseases, and severe genetic disorders.…
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World ADC Awards 2026 Shortlist Announced, Recognizing Excellence Across the ADC Industry

Sep 1, 2026
The World ADC Awards 2026 shortlist has been announced, recognizing the organizations, teams, technologies, and individuals driving innovation and advancing the field of antibody-drug…
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Cipla Licenses HER2 Cancer Drug TQB2102 Across Emerging Markets

Sep 1, 2026
Cipla Limited and Sino Biopharmaceutical’s subsidiary Chia Tai Tianqing Pharmaceutical Group (CTTQ) have entered into an exclusive licensing and supply agreement for TQB2102, an…
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FDA Approves BESREMi for Essential Thrombocythemia After 30 Years

Sep 1, 2026
The U.S. Food and Drug Administration (FDA) has approved PharmaEssentia’s BESREMi (ropeginterferon alfa-2b-njft) for the treatment of adults with essential thrombocythemia (ET), making…
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Teva Discusses Lower Medicaid Drug Prices With Trump Administration

Sep 1, 2026
Teva Pharmaceuticals, the U.S. affiliate of Teva Pharmaceutical Industries Ltd., has announced a shared commitment with the Trump Administration to explore ways to lower the cost of…
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Kazia Therapeutics Raises $40 Million to Advance Paxalisib Trials

Sep 1, 2026
Kazia Therapeutics Limited has closed an oversubscribed public offering that generated approximately $40 million in upfront gross proceeds, providing additional funding for the clinical…
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SK Biopharmaceuticals to In-License Opakalim for Epilepsy Treatment

Aug 31, 2026
SK Biopharmaceuticals has agreed to in-license opakalim, an investigational anti-seizure medicine from Biohaven, in a deal that could reach $795 million and could help the South Korean…
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FDA Accepts Kowa’s K-911 Glaucoma Drug Application for Review

Aug 31, 2026
The U.S. Food and Drug Administration (FDA) has accepted Kowa Pharmaceuticals America’s New Drug Application (NDA) for K-911, an investigational eye drop being developed to reduce…
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