Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Milrinone is a small molecule, non-digitalis, non-catecholamine inotropic agent and vasodilator used primarily for the short-term intravenous treatment of acute decompensated heart failure. It acts as a selective phosphodiesterase 3 (PDE3) inhibitor, increasing intracellular cyclic adenosine monophosphate (cAMP) levels in cardiac and vascular smooth muscle cells. This leads to enhanced myocardial contractility (positive inotropy), improved ventricular relaxation (lusitropy), and vasodilation by reducing both preload and afterload. Milrinone is structurally related to amrinone but is more potent with fewer side effects such as thrombocytopenia. Its onset of action is rapid when administered intravenously, with effects peaking within hours and lasting several hours due to its short half-life[1][5][6][7][8].
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 milrinone.