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...
Kensana Health secured a share subscription facility of up to $120 million with GEM Global Yield, available for 36...
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...
No new efficacy or safety figures were released, but NKGen Biotech plans to present recent clinical data on its...
All 27 patients completed treatment with no serious adverse events in Lipella’s Phase 2a study of LP-10 for oral...
In healthy volunteers, GT-02287 increased glucocerebrosidase (GCase) activity by more than 50% at clinically relevant doses, with plasma and...
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...
Telitacicept delivered a placebo‑adjusted 4.83‑point improvement on MG‑ADL at 24 weeks in a Phase 3 study of generalized myasthenia...