Navepegritide Trial Results for Children with Achondroplasia
TransCon CNP (navepegritide) met the primary endpoint in the 52-week, randomized, double-blind ApproaCH trial, delivering a statistically significant increase...
TransCon CNP (navepegritide) met the primary endpoint in the 52-week, randomized, double-blind ApproaCH trial, delivering a statistically significant increase...
Protara TherapeuticsProtara Therapeutics will present interim safety and efficacy data from 31 BCG‑naïve patients in Cohort A of the...
Phase 1 data for sabirnetug (ACU193) showed a favorable safety profile with low overall rates of ARIA-E and evidence...
Across two double-blind Phase 3 studies in nearly 1,000 adults with fibromyalgia (RELIEF, n=503; RESILIENT, n=457), TONMYA (cyclobenzaprine HCl...
Topline efficacy from ORIC’s Phase 1b mCRPC study shows a 55% PSA50 response rate (11/20) with 40% confirmed (8/20),...
Reported accuracy came in at 95% to 99% across measured parameters in Inspira Technologies’ clinical study and ongoing lab...
Enrollment is complete at 540 participants in START, a randomized, placebo-controlled Phase 2 trial of zervimesine (CT1812) in mild...
An earlier study reported that when combined with PSA, Trinity Biotech’s EpiCapture correctly identified all high-grade prostate cancers in...
Interim results from the CAMPAIGN randomized controlled trial reported a 98.5% posterior probability that lyophilized human amnion/chorion membrane (EPIEFFECT)...
Bioxodes reported encouraging Phase 2a signals for BIOX-101 in intracerebral hemorrhage, including a reduction in hematoma among all treated...