drugset / Trial / NCT01791049

TD-1607 SAD Study in Healthy Subjects

NCT01791049 ↗

Phase 1 Completed 64 enrolled Theravance Biopharma
RandomizedSingle-groupTriple-blindTreatment

Summary

TD-1607, administered intravenously as single doses, will be investigated in healthy subjects to assess its tolerability, safety, and pharmacokinetics.

Timeline

Start
2013-04
Primary completion
2013-08
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject TD-1607 Other / unclassified — Intravenous