Vima’s Hope: First Dystonia Patient Dosed in Phase 2 Study
Phase 1 data for VIM0423 showed the oral agent was safe and well tolerated through 28 days in healthy...
Phase 1 data for VIM0423 showed the oral agent was safe and well tolerated through 28 days in healthy...
SELLAS’ CDK9 inhibitor SLS009 (tambiciclib) previously delivered a 33% overall response rate across evaluable relapsed/refractory AML patients, rising to...
Aplagon has dosed the first patient in HEALING, a Phase 2a study of APAC in chronic limb-threatening ischemia secondary...
Cbio has received regulatory clearance to initiate a first‑in‑human Phase I/IIa study of novoleucel in persistent or recurrent cervical...
Prior data on alpibectir-ethionamide (AlpE) showed a 7-day early bactericidal activity signal comparable to isoniazid and a generally acceptable...
In the PIK3CA wild-type cohort of the Phase 3 VIKTORIA-1 trial in HR+/HER2- advanced breast cancer post-CDK4/6 inhibitor, gedatolisib...
FDA has cleared the first dental‑dedicated MRI system in the U.S., the MAGNETOM Free.Max Dental Edition, following a clinical...
No efficacy or safety figures were disclosed. Profound Medical will present the first clinical outcomes from CAPTAIN, a Level...
A 7-day Phase 2a early bactericidal activity study in pulmonary tuberculosis established clinical proof of concept for alpibectir plus...
Regimen failure through 48 weeks was 22.8% with long-acting cabotegravir plus rilpivirine versus 41.2% with continued daily oral ART...