Corvia Atrial Shunt
Phase 3- Indications
- Heart failure with preserved ejection fraction, Heart failure with mildly reduced ejection fraction
Company intelligence / Profile preview
Corvia Medical has developed the world’s first transcatheter atrial shunt device for treating HFpEF/HFmrEF. The REDUCE LAP-HF II pivotal study did not meet its primary endpoint overall but showed benefit in a narrower patient population. The ongoing RESPONDER-HF confirmatory trial aims to support FDA approval. Over three years of clinical data show favorable long-term effects on cardiac structure and function, and more than 675 patients have received the device across at least 18 countries.
Beyond the preview
Explore clinical development, deal activity, and the competitive landscape with Gosset’s full data platform.
Follow clinical development from trial design and recruitment through results.
Explore licensing agreements, acquisitions, and the assets behind each deal.
Trace financing activity and the investors behind a company’s development.
Compare peer pipelines by target, modality, and therapeutic area.
Explore technology platforms and the patent landscape around relevant assets.
Connect company news and source material to the questions you’re investigating.
See how Gosset can support your research on Corvia Medical.