Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The phrase "dobutamine or milrinone" refers to the selection of intravenous inotropic agents used for the management of patients with severe, decompensated congestive heart failure, particularly those awaiting cardiac transplantation (UNOS Status 1B). Dobutamine is a synthetic catecholamine and a potent beta-1 adrenergic receptor agonist that increases myocardial contractility and cardiac output. Milrinone is a bipyridine phosphodiesterase 3 (PDE3) inhibitor that increases intracellular cyclic adenosine monophosphate (cAMP), leading to enhanced contractility and systemic vasodilation (inodilator effect). In clinical trial contexts, such as the TMAC study for nesiritide, these drugs are used as continuous infusions to provide hemodynamic support as part of standard care.
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 dobutamine or milrinone (Eli Lilly and Company).