drugset / Trial / NCT02183259

Bioavailability, Pharmacokinetics and Safety of ESR 1150 CL in Healthy Adult Male Volunteers

NCT02183259 ↗

Phase 1 Completed 18 enrolled Boehringer Ingelheim
Non-randomizedCrossoverOpen-labelTreatment

Summary

To investigate the bioavailability of ESR 1150 CL by the time course determination of plasma concentration (pharmacokinetics) of no-transformed ESR 1150 after single administration to healthy adult male volunteers. Secondary objective is to investigate the safety of ESR 1150 CL.

Timeline

Start
1998-11
Primary completion
1998-12
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject ESR 1150 CL Unknown 0.015 mg Oral
Subject ESR 1150 CL Unknown 1 mg Oral

Indications

No indication recorded.