Tanabe Pharma on March 30 reported the global PIII results for its investigational oral therapy dersimelagon in erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP), supporting its plans to pursue regulatory filings with the US FDA and, later, in Japan. The…
To read the full story
Related Article
BUSINESS
- Lunsumio Combo Hits PIII Goal in Follicular Lymphoma: Roche
September 18, 2026
- Padcev-Keytruda Gets CHMP Nod for Expanded MIBC Use
September 18, 2026
- SanBio Eyes October Start for Akuugo Treatment
September 18, 2026
- Toho Unit to Launch Pharma-Wholesaler Payment Service
September 18, 2026
- Astellas Names Marino General Counsel, Compliance Chief
September 18, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





