News

FDA has approved perioperative pembrolizumab for resectable head and neck squamous cell carcinoma, but do patients need ...
Pembrolizumab, an immune checkpoint inhibitor, has been approved by the U.S. Food and Drug Administration (FDA) for the ...
Pembrolizumab, an immune checkpoint inhibitor, has been approved by the U.S. Food and Drug Administration (FDA) for the ...
The FDA has granted approval to pembrolizumab for the treatment of adult patients with resectable, locally advanced HNSCC ...
MSD has received US Food and Drug Administration (FDA) approval for its anti-programmed death receptor-1 (PD-1) therapy, ...
Interim results reveal promising efficacy and safety of sacituzumab govitecan and pembrolizumab for muscle-invasive bladder ...
The Phase 1 dose escalation has been completed, and results show encouraging early signs of clinical activity in solid tumors ...
Sacituzumab govitecan plus pembrolizumab improves outcomes vs chemotherapy plus pembrolizumab in patients with previously ...
"These long-term results continue to support [pembrolizumab's] use as a standard of care for patients at increased risk of recurrence," says Naomi B. Haas, MD.
Teva Pharmaceutical ( NYSE: TEVA) and Shanghai Fosun Pharmaceutical announced a collaboration on Monday to develop TEV-56278, a new therapy aimed at treating various cancers through an anti-PD1-IL2 ...
Pembrolizumab significantly reduced the risk of event free survival events by 30% compared with standard of care.