drugset / Trial / NCT02314793

A Study to Assess the Safety, Tolerability and Pharmacokinetics of ASP2205 in Healthy Young Males and Females and Elderly Females and to Evaluate the Effect of Food on the Pharmacokinetics of a Single Dose of of ASP2205

NCT02314793 ↗

Phase 1 Terminated 93 enrolled Astellas Pharma Europe B.V.
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of this study is to evaluate the safety and tolerability of single ascending oral doses of ASP2205 in healthy young male and female subjects. This study will also evaluate the safety and tolerability of multiple ascending oral doses of ASP2205 in healthy young and elderly female subjects.

Timeline

Start
2014-11
Primary completion
2015-10
Completion
2015-10

Outcome

Outcome not reported

Stopped: “The study has been terminated because of operational reasons.”

Drugs

EvaluationDrugModalityDoseRoute
Subject ASP2205 Small molecule — Oral

Indications

No indication recorded.