FDA has approved pembrolizumab marketed as Keytruda by Merck in combination with pemetrexed and platinum chemotherapy as a first-line treatment for adult patients with unresectable advanced or metastatic malignant pleural mesothelioma (MPM). The approval of pembrolizumab + chemotherapy was based on data from the KEYNOTE-483 trial, offering hope for MPM patients without prior systemic therapy. […]...
FDA Approves Atezolizumab-Hyaluronidase-tqjs for NSCLC,...
FDA has approved atezolizumab and hyaluronidase-tqjs developed by, Genentech, for…
FDA Grants ODD to Actuate’s...
FDA has granted Orphan Drug Designation (ODD) to Actuate Therapeutics…
FDA Approves TruSight’ Comprehensive Assay...
FDA has approved Illumina for its TruSight Oncology Comprehensive Assay,…