drugset / Trial / NCT02106247

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Oral Doses of BI 1181181 in Healthy Male Volunteers

NCT02106247 ↗

Phase 1 Completed 36 enrolled Boehringer Ingelheim
RandomizedSingle-groupDouble-blindTreatment

Summary

To assess the reduction of ß-amyloid levels in cerebrospinal fluid and plasma and to evaluate pharmacokinetics, safety and tolerability following single oral doses of BI 1181181.

Timeline

Start
2014-04
Primary completion
2014-06
Completion
2014-06

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1181181 Unknown — Oral

Indications

No indication recorded.