drugset / Trial / NCT02209688

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ESR 1150 CL in Healthy Subjects

NCT02209688 ↗

Phase 1 Terminated 39 enrolled Boehringer Ingelheim
RandomizedCrossoverOpen-labelTreatment

Summary

The objective of this study was to obtain safety and tolerability data and first pharmacokinetic and pharmacodynamic data of escalating doses of ESR 1150 CL.

Timeline

Start
2000-02
Primary completion
2000-03
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject ESR 1150 CL Unknown 0.5 mg —
Subject ESR 1150 CL Unknown 1 mg —
Subject ESR 1150 CL Unknown 2 mg —
Subject ESR 1150 CL Unknown 4 mg —
Subject ESR 1150 CL Unknown 8 mg —

Indications

No indication recorded.