LEO outlays $435m for rights to Tanabe’s rare disease drug for sun-induced pain
Tanabe’s dersimelagon is already under FDA review having achieved positive Phase III results earlier this year.
Tanabe’s dersimelagon is already under FDA review having achieved positive Phase III results earlier this year.
With regulatory conditions tightening around climate impact and environmental persistence of medical propellants, HFA-152a is a practical route to maintain clinical performance, patient outcomes and supply continuity of inhalers. However,...
The pharmaceutical industry continues to be a hotbed of patent innovation. Activity is driven by the evolution of treatment paradigms,...
Bristol Myers, NVIDIA join forces to build life science’s ‘most powerful’ AI factory
Turning AI skeptics into AI advocates through high-integrity data
Keeping pace with generative AI in pharmaceutical and healthcare organisations
Pharma Meets AI Conference 2026: Key barriers to scaling AI in drug development