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NCT04914247 Clinical Trial

Individual Patient Expanded Access IND for Selexipag (Uptravi) in Participants With Non-healing Wound, Buerger's Disease

Non-healing Wound Clinical Trial

Official title:
Individual Patient Expanded Access IND for Selexipag (Uptravi) in Participants With Non-healing Wound, Buerger's Disease

Clinical Trial Details — Status: Available

Administrative data
NCT number NCT04914247
Other study ID # CR108669
Secondary ID
Status Available
Phase
First received
Last updated

Study information
Verified date February 2024
Source Actelion
Contact Contact
Phone 1-800-JANSSEN (1-800-526-7736)
Email Janssenmedinfo@its.jnj.com
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

The purpose of this expanded access program (EAP) is to provide Selexipag (Uptravi) for the treatment of participant with non-healing wound, buerger's disease.

Recruitment information / eligibility

— Not specified —

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Selexipag

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Actelion
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