A Phase 2 Study of the Safety and Efficacy of Brepocitinib in Adults With Cutaneous Sarcoidosis (BEACON)

Last updated: May 9, 2025
Sponsor: Priovant Therapeutics, Inc.
Overall Status: Active - Recruiting

Phase

2

Condition

Sarcoidosis

Treatment

Oral Brepocitinib

Oral Placebo

Clinical Study ID

NCT06978725
PVT-2201-203
  • Ages 18-75
  • All Genders

Study Summary

This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with cutaneous sarcoidosis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Adults subjects (18-74)

  2. Cutaneous sarcoidosis with characteristic skin biopsy histology

  3. A CSAMI activity score ≥ 10

  4. Weight > 40 kg to < 130 kg with BMI < 40 kg/m2 .

Exclusion Criteria

  1. History of
  • Lymphoproliferative disorder

  • Active malignancy;

  • History of cancer within 5 years prior to baseline (exceptions for basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the uterine cervix).

  1. High risk of thrombosis or cardiovascular disease

  2. High risk of herpes zoster

  3. Active or recent infection

Study Design

Total Participants: 28
Treatment Group(s): 2
Primary Treatment: Oral Brepocitinib
Phase: 2
Study Start date:
April 09, 2025
Estimated Completion Date:
December 31, 2026

Connect with a study center

  • Clinical Trial Site

    San Francisco, California 94115
    United States

    Active - Recruiting

  • Clinical Trial Site

    Durham, North Carolina 27703
    United States

    Active - Recruiting

  • Clinical Trial Site

    Philadelphia, Pennsylvania 19104
    United States

    Active - Recruiting

  • Clinical Trial Site

    Madison, Wisconsin 53715
    United States

    Active - Recruiting

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