Ignite Creation Date:
2024-05-06 @ 9:34 AM
Last Modification Date:
2024-10-26 @ 12:16 PM
Study NCT ID:
NCT03016468
Status:
WITHDRAWN
Last Update Posted:
2017-04-11
First Post:
2017-01-06
Brief Title:
Safety of Transition From Selexipag to Remodulin Then Oral Treprostinil in Symptomatic Adult PAH
Sponsor:
United Therapeutics
Organization:
United Therapeutics
Study Overview
Official Title:
A Multicenter 16-Week Open-label Study Evaluating the Safety of Transition From Selexipag to Remodulin Then Oral Treprostinil in Symptomatic Subjects With Pulmonary Arterial Hypertension
Status:
WITHDRAWN
Status Verified Date:
2017-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Business decision
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a multicenter single-arm trial to evaluate the safety of the transition from Selexipag to Remodulin then Oral Treprostinil in Symptomatic Subjects with Pulmonary Arterial Hypertension PAH The study will include about 30 subjects at approximately 10 clinical trial centers The treatment phase of the study will last approximately 16 weeks
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None