Expanded Access to Upadacitinib
Sponsor
AbbVie (Industry)
Overall Status
No longer available
CT.gov ID
NCT04159597
Collaborator
(none)
Study Details
Study Description
Brief Summary
This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to upadacitinib prior to approval by the local regulatory agency. Availability will depend on territory eligibility. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
Study Design
Study Type:
Expanded Access
Official Title:
Expanded Access to Upadacitinib
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- The participant must not be eligible for upadacitinib clinical trial.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- AbbVie
Investigators
- Study Director: AbbVie Inc., AbbVie
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
AbbVie
ClinicalTrials.gov Identifier:
NCT04159597
Other Study ID Numbers:
- C20-082
First Posted:
Nov 12, 2019
Last Update Posted:
Aug 9, 2021
Last Verified:
Aug 1, 2021
Keywords provided by AbbVie
Additional relevant MeSH terms: