Roivant’s mosliciguat cut pulmonary vascular resistance 56% in 16-week Phase 2 study
Topic: healthRegion: globalUpdated: i2 outletsSources: 5Spectrum: Mostly CenterFiltered: Global (0/5)· Clear⏱ 2 min read📡 Wire pickup⚠ 3d+ old
Story Summary
SITUATION
Roivant said mosliciguat reduced pulmonary vascular resistance by 56% versus placebo in a 16-week Phase 2 study. The trial also met key secondary endpoints — a 35-meter placebo-adjusted six-minute walk improvement and a 53% NT-proBNP reduction — which Roivant said could advance treatment and strengthen its finances.
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KEY FACTS
- Roivant reported that mosliciguat achieved a 56% reduction versus placebo in pulmonary vascular resistance in a 16-week Phase 2 study.
- The study duration was 16 weeks and is described as a Phase 2 (mid-stage) trial.
- Roivant characterized the statistically significant results as a potential new treatment approach for pulmonary hypertension and said they could bolster the company’s financial health.
HISTORICAL CONTEXT
Brief
Roivant said its experimental drug mosliciguat achieved the goals of a 16-week Phase 2 study, including a 56% placebo-adjusted reduction in pulmonary vascular resistance. The company said the statistically significant results could open a new treatment approach for pulmonary hypertension and bolster Roivant’s finances.
Sources
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