ResMed launches sleep apnea study in heart failure patients
The international Serve-HF study will focus specifically on the impact of treatment of central sleep apnea (CSA) in patients with heart failure. According to the company, up to
The US Food and Drug Administration (FDA) has expanded the approved indication for Bristol Myers Squibb’s (BMS) Camzyos (mavacamten) to treat symptomatic obstructive hypertrophic cardiomyopathy (oHCM) in adults and paediatric patients weighing at least 30kg (66lb).
Riociguat demonstrated significantly improved exercise capacity in a Phase II study in patients with chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension (PAH) as compared to baseline
Following the recommendation for regulatory approval under the European decentralized procedure, Toctino (alitretinoin) received national regulatory approval in Germany. Marketing applications for the use of alitretinoin in the