Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Potassium canrenoate is a water-soluble, small molecule mineralocorticoid receptor antagonist (MRA) and the primary active metabolite of spironolactone. It functions by competitively inhibiting the mineralocorticoid receptor, thereby blocking the effects of aldosterone and preventing sodium and water retention. In the context of the MINIMISE-STEMI Phase 3 trial led by University College, London, it was investigated as an intravenous pretreatment administered prior to primary percutaneous coronary intervention (PPCI) in patients with ST-elevation myocardial infarction (STEMI). The goal was to reduce myocardial infarct size and prevent adverse left ventricular remodeling. While the trial did not meet its primary endpoint of reducing infarct size, it suggested benefits in preserving cardiac structure. It is clinically available in several European countries but is not FDA-approved.
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 potassium canrenoate.