Roivant Sciences (Nasdaq: ROIV) today announced its previously undisclosed pipeline program mosliciguat, a potential first-in-class, inhaled, once-daily sGC activator with targeted delivery to the lungs via dry powder inhaler, at Pulmovant.
Pulmovant presented data from the proof-of-concept Phase Ib ATMOS study during the ERS Congress in Vienna, Austria.
In the Phase Ib ATMOS study, presented today is a single dose of inhaled mosliciguat in pulmonary hypertension (PH) patients (N=38) led to sustained, clinically-meaningful mean-max reductions in pulmonary vascular resistance (PVR) of up to ~38%, one of the highest reductions seen in PH trials to date.
Once-daily dosing via dry powder inhaler (DPI) was generally well-tolerated, with low rates of treatment-emergent adverse events (TEAEs).
The global Phase II “PHocus” study of mosliciguat in ~120 patients with PH-ILD is expected to begin imminently.
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