drugset / Trial / NCT01949103

TD-1607 MAD Study in Healthy Subjects

NCT01949103 ↗

Phase 1 Completed 48 enrolled Theravance Biopharma
RandomizedSingle-groupQuadruple-blindTreatment

Summary

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

Timeline

Start
2013-10
Primary completion
2014-06
Completion
2014-07

Drugs

EvaluationDrugModalityDoseRoute
Subject TD-1607 Other / unclassified — Intravenous