A Phase 2 Open Label Study to Assess the PK/PD Properties of RUC-4 in Patients With a ST-elevation Myocardial Infarction

PHASE2CompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

June 2, 2020

Primary Completion Date

November 8, 2020

Study Completion Date

December 14, 2020

Conditions
Coronary DiseaseMyocardial InfarctionHeart DiseasesVascular DiseasesSTEMI - ST Elevation Myocardial Infarction
Interventions
DRUG

RUC-4 Compound

All patients will receive a single subcutaneous dose of RUC-4 in the Cardiac Catheterization Lab (CCL) before coronary angiography/percutaneous coronary intervention.

Trial Locations (1)

3435

St. Antonius hospital, Nieuwegein

Sponsors
All Listed Sponsors
collaborator

St. Antonius Hospital

OTHER

collaborator

Diagram B.V.

OTHER

lead

CeleCor Therapeutics

INDUSTRY

NCT04284995 - A Phase 2 Open Label Study to Assess the PK/PD Properties of RUC-4 in Patients With a ST-elevation Myocardial Infarction | Biotech Hunter | Biotech Hunter