Innocare IND Approval For New VAV1 Degrader Trial In China
InnoCare Pharma has received CDE approval from China’s NMPA to begin clinical trials of ICP-538, an oral VAV1-directed molecular...
InnoCare Pharma has received CDE approval from China’s NMPA to begin clinical trials of ICP-538, an oral VAV1-directed molecular...
Enrollment targets are modest but specific: 50–100 anonymous survey responses and 10–20 confidential interviews, backed by Columbia University IRB...
Interim data from Dogwood Therapeutics’ ongoing Phase 2b HALT-CINP study point to a favorable operational and clinical signal: a...
In early clinical testing, a single inhaled dose of mosliciguat reduced pulmonary vascular resistance by up to 38% and...
Feasibility data published in 2025 reported immediate, sustained increases in blood pressure with implant-based spinal cord stimulation in people...
One-year overall survival exceeded 80% across all mismatch levels in the prospective, 268-patient ACCESS trial of mismatched unrelated donor...
Dewpoint Therapeutics has dosed the first patient in a Phase 1a/2a study of DPTX3186, a first-in-class small molecule that...
Congress’s 2026 appropriations package for HHS embeds a clear directive: FDA and NIDA are to collaborate on alternative clinical...
Treatment-naïve infants with SMA receiving Biogen’s higher-dose nusinersen regimen achieved a 26.19-point advantage on CHOP-INTEND versus a prespecified matched...
Global Phase 3 data for 177Lu‑PSMA‑I&T have met the primary endpoint with statistically significant, clinically meaningful benefit in metastatic...