Viewing Study NCT02223832



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Last Modification Date: 2024-10-26 @ 11:29 AM
Study NCT ID: NCT02223832
Status: COMPLETED
Last Update Posted: 2014-08-22
First Post: 2014-08-21

Brief Title: Study to Evaluate the Pharmacokinetics Tolerability and Safety of ACT-128800 in Japanese and Caucasian Healthy Male and Female Subjects
Sponsor: Actelion
Organization: Actelion

Study Overview

Official Title: Single-center Open-label Parallel-group Study to Evaluate the Pharmacokinetics Tolerability and Safety of a Single Dose of 40 mg ACT-128800 in Japanese and Caucasian Healthy Male and Female Subjects
Status: COMPLETED
Status Verified Date: 2014-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a study to evaluate the relative pharmacokinetic properties and the tolerability and safety of ACT-128800 in Japanese and Caucasian healthy male and female subjects after single-dose administration
Detailed Description: 10 Japanese and 10 Caucasian healthy male and female subjects in a one to one male to female ratio will be included in the study Japanese and Caucasian subjects will be matched for body weight

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None