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

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorPriovant Therapeutics, Inc.

About this trial

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

Eligibility criteria

Qualifiers

Adults subjects (18-74)

Cutaneous sarcoidosis with characteristic skin biopsy histology

A CSAMI activity score ≥ 10

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

Disqualifiers

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).

Trial design

Treatments tested in this trial

  • Oral Brepocitinib
  • Oral Placebo

Treatment groups

28 Participants
are divided into 3 treatment groups

Locations

4
Clinical Trial Site94115, San FranciscoCalifornia, United States
Clinical Trial Site27703, DurhamNorth Carolina, United States
Clinical Trial Site19104, PhiladelphiaPennsylvania, United States
Clinical Trial Site53715, MadisonWisconsin, United States

Sponsors and collaborators

Priovant Therapeutics, Inc.

Lead sponsor