A Study of a Single Dose of ASP3291 in Subjects With Ulcerative Colitis

Status Completed

Clinical Trial Summary

The purpose of this study is to determine the pharmacokinetics (PK) and to assess safety and tolerability of a single dose of ASP3291 in subjects with ulcerative colitis.

Clinical Trial Description

After an 11-day screening period, subjects check into a clinic, are dosed on Day 1 and stay in the clinic for 4 days to monitor pharmacokinetic and safety parameters. ;

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01320332
Study type	Interventional
Source	Telsar Pharma Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	August 2010
Completion date	August 2011

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