Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Idrevloride (VX-371) is an investigational, inhaled small-molecule inhibitor of the epithelial sodium channel (ENaC), developed by Parion Sciences in collaboration with Vertex Pharmaceuticals. It is primarily being developed for the treatment of primary ciliary dyskinesia (PCD), a genetic disorder characterized by impaired mucociliary clearance. By blocking ENaC on the airway surface, idrevloride prevents the excessive absorption of sodium and water, thereby increasing the volume of airway surface liquid. This hydration of the mucus layer facilitates easier clearance of secretions. In clinical studies, such as the Phase 2 CLEAN-PCD trial, idrevloride has been evaluated as a nebulized solution, often in conjunction with hypertonic saline, showing significant improvements in lung function.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on idrevloride.