VenoValve
Phase 3- Indications
- Chronic Venous Insufficiency
Company intelligence / Profile preview
The company’s lead product, VenoValve®, has completed patient enrollment in its U.S. pivotal SAVVE® trial for severe deep venous CVI and has reported positive topline efficacy data at six months, showing significant clinical improvement and meaningful benefit. The device awaits FDA premarket approval submission. A second program, enVVe™, a non-surgical transcatheter valve system, is preparing for first-in-human trials. Both products are investigational and not yet approved or cleared for any indication.
1 more asset in the full pipeline.
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