The aim of our study was to compare the time to conversion and the conversion rate within 90 min in patients with recent-onset atrial fibrillation treated with vernakalant or ibutilide.
Cardiome Pharma has announced the publication of results from an open label, single-center, randomized controlled study conducted by independent researchers...
Cardiome Pharma Corp. announced that it has received a response from the FDA regarding the regulatory path for Brinavess (vernakalant...
Correvio Pharma has resubmitted a New Drug Application (NDA) to the US FDA seeking approval for Brinavess (vernakalant hydrochloride, IV),...
This study evaluates the efficacy and safety of dupilumab in patients with severe chronic rhinosinusitis with nasal polyps (CRSwNP). It demonstrates significant improvements in nasal polyp size, sinus opacification, and symptom severity.
Merck & Co has returned the global marketing and development rights to Cardiome Pharma Corporation for both the intravenous and...
Novartis announced new late-breaking data from the head-to-head CLEAR study, demonstrating that Cosentyx (secukinumab) remains superior to Stelara (ustekinumab) in...
New data confirms RoActemra/Actemra (tocilizumab), from Genetech/Roche, is superior to Humira (adalimumab) in achieving disease remission in Rheumatoid Arthritis patients...
FDA issues complete response letter for Cardamyst nasal spray for PSVT conversion. Milestone Pharma's update.
UCB announced positive results from the Phase IIIb BE RADIANT study, a direct comparison of the investigational IL-17A and IL-17F inhibitor, bimekizumab, to the IL-17A inhibitor, Cosentyx (secukinumab) in the treatment of adult patients with moderate-to-severe plaque psoriasis.