Rein Therapeutics Doses First Patient in Phase 2 IPF Trial
Rein Therapeutics has dosed the first patient in a randomized, double-blind, placebo-controlled Phase 2 trial of LTI-03 in idiopathic...
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Rein Therapeutics has dosed the first patient in a randomized, double-blind, placebo-controlled Phase 2 trial of LTI-03 in idiopathic...
FDA accepted physiologically based pharmacokinetic (PBPK) predictions generated with Certara’s Simcyp platform in lieu of at least ten dedicated...
Arcutis has enrolled the first participant in ARQ-234-131, a Phase 1a/1b, double-blind, randomized, placebo-controlled, first-in-human study of ARQ-234, a...
Near-100% source-to-EDC data accuracy, roughly 90% faster data entry at sites, and adoption across more than 2,500 research sites...
No serious adverse events were reported and overall tolerability remained favorable in Clearmind Medicine’s second cohort of its Phase...
No quantitative efficacy data were disclosed, but AIM ImmunoTech reports positive progression-free survival, overall survival, and safety signals from...
No efficacy or safety outcomes have been reported yet. The development moves into humans with MHRA approval for a...
In real-world data from the Innovations in Genicular Outcomes Registry, patients who received liposomal bupivacaine during total knee arthroplasty...
FDA has lifted the clinical hold on Intellia’s Phase 3 MAGNITUDE trial of nexiguran ziclumeran in ATTR-CM after a...
EyePoint has begun dosing in two global Phase 3 trials, COMO and CAPRI, evaluating DURAVYU (vorolanib intravitreal insert) in...