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A Study Evaluating BFB759 in Moderate to Severe Hidradenitis Suppurativa

Study acronym: COMPASS 2-HS
StatusActive, Not Recruiting
PhasePhase 2/3
Started
View on ClinicalTrials.gov ↗

Record History

  1. Enrollment closed, study ongoing Eligibility criteria expanded, about 6 words · Secondary endpoints: details revised at 5 of 5 entries · Site details revised at 58 of 58 sites Show 3 more changesShow less
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: details revised at 5 of 5 entries
    • Site details revised at 58 of 58 sites
  2. Trial sites expanded: 33 → 58 locationsv3
  3. Study sites: 4 to 33v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a double-blind, placebo-controlled study where subjects are participating for approximately 36 to 40 weeks. The study compares how well BFB759 works and how safe it is compared with a placebo.
Trial Details
NCT Number NCT07287644
Lead Sponsor Bluefin Biomedicine, Inc.
Conditions Hidradenitis Suppurativa (HS)
Enrollment 210 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov