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QIAGEN and Myriad Genetics Team Up to Create Global HRD Test for Research and Companion Diagnostics
Friday, May 31, 2024QIAGEN and Myriad Genetics have announced a partnership to create a globally distributable kitbased test for analyzing Homologous Recombination Deficiency status This nextgeneration sequencing test aims
Dupilumab (Dupixent) Recommended for COPD Treatment Approval by EU CHMP
Friday, May 31, 2024Regeneron Pharmaceuticals Inc and Sanofi have jointly announced that the European Medicines Agencys Committee for Medicinal Products for Human Use has issued a favorable opinion recommending the approval of Dupixent in the European Union
Larimar Therapeutics Receives FDA Nod to Join START Pilot Program for Nomlabofusp in Friedreich’s Ataxia
Friday, May 31, 2024Larimar Therapeutics Inc a company in the biotechnology sector focusing on rare diseases has announced that the FDA has selected nomlabofusp to participate in the Support for Clinical Trials Advancing Rare
BioNTech and CEPI Partner to Enhance Africa's mRNA Vaccine Ecosystem
Thursday, May 30, 2024BioNTech SE and the Coalition for Epidemic Preparedness Innovations are expanding their strategic partnership to establish a robust and sustainable vaccine manufacturing ecosystem in Africa CEPI will provide up to million to support BioNTech in sett...
Fusion Pharmaceuticals Acquisition by AstraZeneca Gets Shareholder Approval
Thursday, May 30, 2024Fusion Pharmaceuticals Inc a company in the field of oncology focusing on the development of advanced radio conjugates as targeted therapies made an announcement today regarding the results of a special virtual meeting of its shareholders At this me...
Roche's Inavolisib Receives FDA Priority Review for Advanced Hormone Receptor-Positive, HER2-Negative Breast Cancer with PIK3CA Mutation
Thursday, May 30, 2024Roche announced today that the US Food and Drug Administration has accepted its New Drug Application and granted Priority Review to inavolisib an investigational oral therapy in combination with palbociclib
Aprea Therapeutics' Safety Review Committee Approves 800 mg Dosing of ATRN-119 in ABOYA-119 Trial
Wednesday, May 29, 2024Aprea Therapeutics Inc a clinicalstage biopharmaceutical company focused on precision oncology through synthetic lethality announced that the Safety Review Committee
Cytek® Biosciences Gains Approval for 1-Laser and 2-Laser 6-Color TBNK Reagents for Clinical Use in China
Wednesday, May 29, 2024Cytek Biosciences Inc has announced that its laser and laser color TBNK reagent cocktails have received approval from the China National Medical Products Administration for clinical diagnostic use on the Cytek
FDA Approves Initial Interchangeable Biosimilar for Two Rare Conditions
Wednesday, May 29, 2024Today the US Food and Drug Administration authorized Bkemv as the inaugural interchangeable biosimilar to Soliris for treating specific rare diseases Bkemv has been endorsed for treating the following indications which are presently also approved for...
FDA Prioritizes Review of Sarclisa for Newly Diagnosed Multiple Myeloma Patients Excluded from Transplant Eligibility
Tuesday, May 28, 2024The US Food and Drug Administration has given priority review status to the Supplemental Biologics License Application for Sarclisa in combination with bortezomib lenalidomide and dexamethasone
