Skip to content

Expanded Access to Upadacitinib

Expanded Access to Upadacitinib

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT04159597
Enrollment
Unknown
Registered
2019-11-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alopecia Areata, Atopic Dermatitis, Axial Spondyloarthritis, Crohn Disease, Giant Cell Arteritis, Hidradenitis Suppurativa, Idiopathic Arthritis (Including sJIA, pJIA, or JPsA), Non-radiographic Axial, Non Segmental Vitiligo, Psoriatic Arthritis, Rheumatoid Arthritis, Spondyloarthritis, Systemic Lupus Erythematosus, Ulcerative Colitis

Keywords

Expanded Access, Pre-approval Access, Compassionate Use, Special Access Program, Named Patient Basis, Special Access Scheme

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.

Interventions

DRUGUpadacitinib

Upadacitinib will be administered as oral solution.

Sponsors

AbbVie
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Exclusion criteria

* There are other suitable treatment options. * The participant qualifies for ongoing clinical trials.

Contacts

CONTACTABBVIE CALL CENTER
abbvieclinicaltrials@abbvie.com844-663-3742
STUDY_DIRECTORABBVIE INC.

AbbVie

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 21, 2026