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CompletedNCT01124747

A Study to Assess the Systemic Disposition of ASP1585 After Administration of 14C-labeled Drug

An Open-Label Study to Evaluate the Disposition of 14C-Labeled ASP1585 in Healthy Male Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Astellas Pharma Inc · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to assess the systemic disposition of ASP1585 after oral administration of 14C-labeled drug in healthy male subjects.

Detailed description

Subjects will receive study drug for 18 days with a radioactive dose of study drug given on Day 15. Blood, urine and feces will be collected to confirm recovery of radioactivity.

Conditions

Interventions

TypeNameDescription
DRUGASP1585Oral
DRUG14C-Labeled ASP1585Oral

Timeline

Start date
2010-04-01
Primary completion
2010-05-01
Completion
2010-05-01
First posted
2010-05-17
Last updated
2014-05-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01124747. Inclusion in this directory is not an endorsement.

A Study to Assess the Systemic Disposition of ASP1585 After Administration of 14C-labeled Drug (NCT01124747) · Clinical Trials Directory