C4’s Cemsidomide Data Supports Best-in-Class Myeloma Drug
C4 Therapeutics reported a 50% overall response rate at 100 µg and 40% at 75 µg for cemsidomide plus...
C4 Therapeutics reported a 50% overall response rate at 100 µg and 40% at 75 µg for cemsidomide plus...
No serious adverse events, no discontinuations due to adverse events, and no neuropsychiatric safety signals were observed in a...
In a Phase 2 sub-analysis of HPV16-positive first-line recurrent or metastatic head and neck squamous cell carcinoma with low...
Enrollment in Intellia’s global Phase 3 HAELO trial for lonvoguran ziclomeran (lonvo-z; NTLA-2002) is complete nine months after first...
FDA granted Fast Track designation to Minovia’s autologous mitochondrial cell therapy MNV-201 for myelodysplastic syndromes, adding a second expedited...
In a 268‑patient Phase 3 trial spanning the U.S., Europe, Japan, and Brazil, efzofitimod did not meet its primary...
Mapi Pharma has enrolled the first patient in a multinational Phase I/II study of its once-monthly injectable cariprazine for...
The UK’s MHRA has granted Clinical Trial Authorisation for NVG-222, clearing a first-in-human, Phase I/II adaptive basket study in...
Phase 1 data for TNX-4800 (mAb 2217LS) showed safety and tolerability with a linear pharmacokinetic:pharmacodynamic: efficacy relationship, supporting dose...
No efficacy or safety data were released. Kalaris has begun enrolling a Phase 1b/2 multiple ascending dose study of...