FDA approves Takeda and Orexigen’s Contrave for chronic weight management
The approval allows the tablets for use in chronic weight management in adults with an initial body mass index (BMI) of 30 kg/m2 or greater (obese), or 27
Bristol Myers Squibb (BMS) is set to merge its separate research and development (R&D) departments into a single entity, effective from 1 January 2027.
The Company will use the information generated to advance one or more candidates into formal development studies in the coming months. Prosonix’ MCP Technology allows the combination of
These grants support a global intellectual property estate broadly covering the Company’s biochemistry and delivery technologies with over 100 issued or allowed patents and over 90 pending U.S.
The supplement features a discussion on available clinical evidence from trials conducted in patients with diabetic foot ulcers (DFUs). The authors, Dr. Lawrence Lavery, Professor of Surgery, University
Paul DiTullio, Vice President, Product Development remarked, "The major advantages of the Company’s nanoRNA technology over other antisense, gene-silencing and RNAi technologies is a proprietary chemistry that overcomes
The Phase III PIONEER I trial showed that Humira is effective in reducing common clinical signs and symptoms in moderate-to-severe HS, specifically the number of abscesses and inflammatory