TRIANA Biomedicines doses first patient in groundbreaking ALK+ lung cancer trial
The global, first-in-human, open-label trial will assess the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity of TRI-611
The global, first-in-human, open-label trial will assess the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity of TRI-611
The facility supports drug discovery, biomolecular research, and the development of next-generation diagnostics
The initiative provides clearer regulatory guidance and a defined path from research in space to patient access on Earth
Starting January 1, 2027, Lilly’s Zepbound (tirzepatide), Mounjaro (tirzepatide), and orforglipron, if approved, will be available through participating Medicare Part D plans
Asahi Kasei Pharma receives worldwide exclusive rights for the research, development, manufacturing, and marketing of the active ingredients
The recommendation is based on new data from continuous safety monitoring of medicines in the EU
PreemieFort Enteral Solution's approval marks the first time a nutritional product derived from human milk has been recognized as a prescription medicine anywhere in the world
The upcoming Phase I trial will test the safety, tolerability, and pharmacokinetics of ISM8969 in healthy volunteers and determine the optimal dosing for future studies
EMA recommended 30 veterinary medicines for marketing authorisation in 2025
Subscribe To Our Newsletter & Stay Updated