Open-label Trial of Tofacitinib in Cutaneous Sarcoidosis and Granuloma Annulare
Part of paid clinical trials in New Haven, Connecticut.
- Sponsor
- Yale University
- Study ID
- NCT03910543
- Phase
- PHASE1
- Status
- Completed
Conditions
- Cutaneous Sarcoidosis
- Granuloma Annulare
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Tofacitinib 5 mg twice daily — DRUGTofacitinib will be administered at a dose of 5 mg twice daily
Study Details
To investigate the ability of tofacitinib, a Janus kinase (JAK) inhibitor, to treat patients with cutaneous sarcoidosis and granuloma annulare during 6 months of therapy.
Key Dates
- Start date
- Apr 11, 2019
- Status verified
- Jul 2021
- Primary completion
- Jun 1, 2021
- Completion
- Jun 1, 2021
Study Design
- Enrollment
- 15 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Patients with Cutaneous SarcoidosisPatients with cutaneous sarcoidosis that may also have also have internal organ sarcoidosis
- Experimental: Patients with Granuloma AnnularePatients with granuloma annulare that is long-standing and/or widespread
Primary Outcome Measure
Change in Cutaneous Sarcoidosis Activity and Morphology Instrument (CSAMI) [ Time Frame: 6 - 12 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Yale Center for Clinical Investigation | New Haven | Connecticut | 06519 | - |
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