drugset / Trial / NCT01650155

Single Rising Dose Study With Intravenous Infusion and Subcutaneous Injection of BI 1005273 in Healthy Male Volunteers.

NCT01650155 ↗

Phase 1 Completed 88 enrolled Boehringer Ingelheim
RandomizedSingle-groupSingle-blindTreatment

Summary

To investigate the safety and tolerability of BI 1005273 in healthy male volunteers following intravenous (i.v.) infusion of single rising doses and subcutaneous (s.c.) injection. Secondary objectives are the exploration of the pharmacokinetics and early pharmacodynamics of BI 1005273.

Timeline

Start
2012-07
Primary completion
2014-09
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1005273 Unknown — Subcutaneous
Subject BI 1005273 Unknown — Intravenous

Indications

No indication recorded.