drugset / Trial / NCT02125435

A Dose Escalation Study to Assess the Safety, Tolerability, and Pharmacokinetics of ASP2408 Following Single Intravenous Doses in Healthy Subjects

NCT02125435 ↗

Phase 1 Completed 65 enrolled Astellas Pharma Global Development, Inc.
RandomizedParallel-groupDouble-blindBasic science

Summary

The objective of this study is to assess the safety, tolerability, and pharmacokinetics (PK) of single ascending intravenous (IV) doses of ASP2408 in non-elderly, healthy male and female subjects and to evaluate the pharmacodynamics of ASP2408.

Timeline

Start
2011-01
Primary completion
2012-05
Completion
2012-05

Drugs

EvaluationDrugModalityDoseRoute
Subject ASP2408 Unknown — Intravenous

Indications

No indication recorded.