Camp4’s Pioneering SYNGAP-1 Drug Enters Toxicology Studies
CAMP4 Therapeutics has begun GLP toxicology studies for CMP-SYNGAP-01, an intrathecally delivered antisense oligonucleotide designed to upregulate SYNGAP1 expression...
CAMP4 Therapeutics has begun GLP toxicology studies for CMP-SYNGAP-01, an intrathecally delivered antisense oligonucleotide designed to upregulate SYNGAP1 expression...
After completing the initial 30 mCi cohort with acceptable safety, pharmacokinetics, and biodistribution, the Phase 1 HEAT study of...
Kura Oncology and Kyowa Kirin have dosed the first patient in a new cohort of the Phase 1b KOMET-007...
A 20-patient, single-site U.S. pilot has begun enrolling at Johns Hopkins under an FDA IDE to evaluate the safety...
Topline: In a multicenter registry of 91 critically ill pediatric patients treated with the Aquadex ultrafiltration system, 92% survived...
Silexion reported new preclinical data showing its RNAi candidate SIL204 inhibited proliferation by 83.5% to 99.7% across 11 human...
Vivex Biologics has dosed the first patient in Restore, a randomized, double‑blind, sham‑controlled U.S. trial of VIA Disc NP...
In an interim readout from the Phase 1b CLOVER-2 study in relapsed/refractory pediatric high-grade glioma (pHGG), patients receiving at...
Reunion Neuroscience’s RECONNECT Phase 2 trial in postpartum depression met its primary endpoint with a clinically meaningful reduction in...
Phase 1 data for KYN-5356 showed an acceptable safety and tolerability profile, adequate CNS penetration, dose-dependent reductions of kynurenic...