A Study of Brepocitinib in Adults With Cutaneous Sarcoidosis
Priovant Therapeutics, Inc. · NCT06978725
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2, Phase 3
- Target enrollment
- 168
- US sites recruiting
- 39
- Study start
- April 9, 2025
- Record last updated
- October 21, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with cutaneous sarcoidosis.
Being studied: Oral Brepocitinib; Oral Placebo
Conditions: Cutaneous Sarcoidosis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Adults subjects
- Cutaneous sarcoidosis with characteristic skin biopsy histology
- A CSAMI activity score ≥ 10
- Weight > 40 kg to \< 130 kg, and with a body mass index (BMI) ≤ 45 kg/m2.
Exclusion Criteria
- History of cancer, with the exception of the following cancers with documentation of complete resection and no evidence of recurrence for ≥ 1 year: basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the uterine cervix.
- High risk of thrombosis or cardiovascular disease
- High risk of herpes zoster
- Active or recent infection
Recruiting US locations
Clinical Trial Site
Birmingham, AL 27516
Clinical Trial Site
Phoenix, AZ 85054
Clinical Trial Site
Tucson, AZ 85718
Clinical Trial Site
San Francisco, CA 94115
Clinical Trial Site
New Haven, CT 06519
Clinical Trial Site
Washington D.C., DC 10060
Clinical Trial Site
Atlanta, GA 30322
Clinical Trial Site
Sandy Springs, GA 30328
Clinical Trial Site
Chicago, IL 60612
Clinical Trial Site
Chicago, IL 60637
Clinical Trial Site
Kansas City, KS 66160
Clinical Trial Site
Louisville, KY 40241
Clinical Trial Site
New Orleans, LA 41076
Clinical Trial Site
Baltimore, MD 21201
Clinical Trial Site
Boston, MA 02115
Clinical Trial Site
Ann Arbor, MI 48103
Clinical Trial Site
Ann Arbor, MI 48109
Clinical Trial Site
Troy, MI 48084
Clinical Trial Site
St Louis, MO 63110
Clinical Trial Site
Lebanon, NH 03766
Clinical Trial Site
Brooklyn, NY 11203
Clinical Trial Site
Lake Success, NY 11042
Clinical Trial Site
New York, NY 10016
Clinical Trial Site
New York, NY 10029
Clinical Trial Site
Rochester, NY 14620
Clinical Trial Site
Chapel Hill, NC 27516
Clinical Trial Site
Durham, NC 27703
Clinical Trial Site
Greenville, NC 27834
Clinical Trial Site
Cleveland, OH 44195
Clinical Trial Site
Fairborn, OH 45324
Clinical Trial Site
Hershey, PA 17033
Clinical Trial Site
Philadelphia, PA 19104
Clinical Trial Site
Philadelphia, PA 19140
Clinical Trial Site
Charleston, SC 29425
Clinical Trial Site
Houston, TX 77030
Clinical Trial Site
Norfolk, VA 23502
Clinical Trial Site
Richmond, VA 23219
Clinical Trial Site
Madison, WI 53715
Clinical Trial Site
Milwaukee, WI 53226
Study contacts (from the official record)
- Clinical Trial Administrator · (212) 634-9743 · clinicaltrials@priovant.com