WHO ICTRP trial
A study to investigate the safety and efficacy of a six month oral treatment…
EUCTR2016-002167-33-ES · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2016-002167-33-ES |
|---|---|
| Public title | A study to investigate the safety and efficacy of a six month oral treatment with a twice daily dose of BAY 1142524 in comparison to placebo in patients with reduced left-ventricular ejection fraction after acute myocardial infarction |
| Scientific title | A randomized, double-blind multicenter study to assess the safety and efficacy of a six month oral treatment with the chymase inhibitor BAY 1142524 at a dose of 25 mg BID in comparison to placebo on top of standard of care in patients with reduced left-ventricular ejection fraction (LVEF = 45%)… |
| Primary sponsor | Bayer AG |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no |
| Countries | Czech Republic;Spain;Israel;Germany;Italy |
| Conditions | Left-ventricular dysfunction after acute myocardial infarction;Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14] |
| Interventions | Product Name: BAY1142524 25mg tablets Product Code: BAY1142524 Pharmaceutical Form: Film-coated tablet INN or Proposed INN: not yet assigned Current Sponsor code: BAY 1142524 Other descriptive name: BAY 1142524 Concentration unit: mg… |
| Registration date | Sep 9, 2016 |
| Target size | 140 |
| Secondary IDs | BAY1142524/16673;2016-002167-33-CZ |
| Registry page | clinicaltrialsregister.eu |
At a glance
- No Results available
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: