Bovie Medical wins FDA clearance for Seer tissue resection device
The Seer device uses conductive sintered steel as an electrode for radio frequency (RF) for cutting and coagulation. The process involves delivery of RF current and sterile saline
Daiichi Sankyo and Merck & Co (MSD) have voluntarily withdrawn their biologics license application (BLA) for ifinatamab deruxtecan, aimed at treating adult patients with extensive-stage small cell lung cancer (ES-SCLC) following disease progression after platinum-based chemotherapy.
The study achieved statistical and clinical significance in its primary efficacy endpoint. Patients receiving the combination of twice-daily mitiglinide and metformin experienced a statistically significant additional reduction in
The multi-center, randomized, double-blinded, placebo-controlled study evaluated the safety and efficacy of the company’s 3% diclofenac diethanolamine NanoEmulsion cream in 104 patients with chronic pain due to osteoarthritis