Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Enoximone is a selective phosphodiesterase type 3 (PDE3) inhibitor with positive inotropic and vasodilator properties, used primarily for the short-term treatment of congestive heart failure. It increases cardiac contractility and dilates blood vessels without significantly increasing myocardial oxygen consumption. The drug acts by inhibiting PDE3, leading to increased intracellular cyclic AMP levels, which enhances calcium flux in cardiac muscle cells and promotes vascular smooth muscle relaxation. Enoximone is administered intravenously or orally, has a bioavailability of about 50%, is metabolized hepatically, and has an elimination half-life of approximately 4–10 hours. While development was discontinued in the U.S., it remains approved for use in several countries including the UK[1][2][4][5][6].
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 enoximone.