RegulationApprovals September 22, 2022 Lilly’s Retevmo receives FDA approval to treat solid tumours By PBR Staff Writer Retevmo (selpercatinib, 40 mg & 80 mg capsules) is indicated to treat locally advanced or metastatic solid tumours in adult patients with a rearranged during transfection (RET) gene
Drug DiscoveryResearch & Development September 21, 2022 NETRIS Pharma, Orano and CLB partner to develop new radio-conjugates By PBR Staff Writer As part of the partnership deal, the entities will initially plan to conduct a preclinical proof-of-concept efficacy study with the new radio-conjugate targeting Netrin-1, combining Netris’ NP137 with
Research & Development September 20, 2022 FDA accepts for priority review Seagen’s sNDA for colorectal cancer medicine By PBR Staff Writer The company is seeking approval for tukysa and trastuzumab combination for the treatment of HER2-positive colorectal cancer in adult patients who have received at least one treatment regimen
RegulationApprovals September 19, 2022 Kite’ Yescarta gets CHMP positive opinion to treat large B-cell lymphoma By PBR Staff Writer Yescarta is a chimeric antigen receptor (CAR) T-cell therapy that is indicated to treat diffuse large B-cell lymphoma (DLBCL) and high-grade B-cell lymphoma (HGBL) in adult patients whose
Drug DiscoveryResearch & Development September 16, 2022 NeuroBo signs license deal with Dong-A ST to develop two drug candidates By PBR Staff Writer Under the deal terms, NeuroBo will undertake the development, regulatory and commercial works for the two therapies across the world excluding certain Asian-Pacific areas. Dong-A will be responsible
Research & Development September 15, 2022 Coave, IMN partner to develop gene therapy for neurodegenerative disorders By PBR Staff Writer Established in January 2011, IMN is a joint research unit of the University of Bordeaux and the French National Centre of Scientific Research (CNRS). The collaboration will focus
Research & Development September 14, 2022 Novome raises funds to advance microbes’ pipeline By PBR Staff Writer Led by Tencent, the financing round has seen participation of new investors including Touchdown Ventures, Colorcon Ventures, Navian Investments, and University of Minnesota. Additionally, Alexandria Venture Investments, 5AM
RegulationApprovals September 13, 2022 AnHeart, NewG Lab receive orphan drug designation in Korea for NSCLC therapy By PBR Staff Writer The Ministry of Food and Drug Safety (MFDS) in Republic of Korea granted the designation to taletrectinib to treat NSCLC)in adult patients. Taletrectinib has been designed for effectively
Drug Manufacturing September 12, 2022 Celregen signs license deal with Cellusion for bullous keratopathy therapy By PBR Staff Writer Under the deal terms, Celregen will gain the exclusive right for the development, production, and commercialisation of CLS001 to treat bullous keratopathy in the Greater China region, including
RegulationApprovals September 9, 2022 US FDA approves Revance’s Daxxify for injection to treat frown lines By PBR Staff Writer Daxxify for injection is a neuromuscular blocking agent and an acetylcholine release inhibitor, which is indicated to temporarily improve moderate to severe glabellar lines’ appearance related to corrugator