drugset / Trial / NCT00543946

Single Ascending Dose of GAP-134 as a 24-hour IV Infusion in Healthy Japanese Males

NCT00543946 ↗

Phase 1 Completed 56 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedSingle-groupSingle-blindPrevention

Summary

This is a study of GAP-134, an antiarrhythmic di-peptide. This study will provide an initial assessment of the safety, tolerability, and pharmacokinetics (PK) of GAP-134 after administration of ascending single intravenous (IV) doses to healthy Japanese male subjects.

Timeline

Start
2007-10
Primary completion
2008-03
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Danegaptide Peptide — Intravenous