CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 48 enrolled
Drug / intervention
Selatogrel 8 mg +1 moredrug
Likely dose
Selatogrel 8 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03487445
NCT03487445Phase 2Completed

A Multi-center, Open-label, Randomized, Study to Assess the Onset of Platelet Aggregation Inhibition After a Single Subcutaneous Injection of ACT-246475 in Adults With Acute Myocardial Infarction

Viatris Innovation GmbH·interventional·Posted Apr 4, 2018·Updated Jul 9, 2025

In Brief

A Phase 2 clinical trial evaluating Selatogrel 8 mg and Selatogrel 16 mg for Acute Myocardial Infarction. Completed, enrolled 48 participants across 6 sites in 3 countries.

Detailed Summary

The goal of this study is to find out how fast a drug called selatogrel (ACT-246475) can prevent platelets from binding together. This study will also help to find out more about the safety of this new drug. The drug selatogrel (ACT-246475) will be used in 2 different doses (8 mg or 16 mg) and will be administered in the thigh.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, Israel, Switzerland
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedApr 4, 2018
Enrollment StartJul 10, 2018
Primary CompletionNov 10, 2018
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 8.2 years ago

Interventions

Selatogrel 8 mgdrug

Selatogrel is a reversible P2Y12 receptor antagonist for subcutaneous administration. It is supplied in sealed glass vials at a strength of 20 mg. The vials with ACT-246475A (hydrochloride salt of ACT-246475) will be reconstituted with 1 mL of water and further diluted with 1 mL sodium chloride (NaCl) 0.9%.

Selatogrel 16 mgdrug

Selatogrel is a reversible P2Y12 receptor antagonist for subcutaneous administration. It is supplied in sealed glass vials at a strength of 20 mg. The vials with ACT-246475A (hydrochloride salt of ACT-246475) will be reconstituted with 1 mL of water for injection.