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Recruiting NCT07783542

ORKA-002 Versus Placebo in Participants With Moderate-to-Severe Hidradenitis Suppurativa

Conditions: Hidradenitis Suppurativa (HS)

Sex: All
Ages: 18 Years – 79 Years
Healthy volunteers: No
Phase: PHASE2
Enrollment: 200
Sponsor: Oruka Therapeutics, Inc.

Location: Oruka Therapeutics Investigative Site Chapel Hill North Carolina

Summary

This is a multicenter, randomized, double-blinded, placebo-controlled clinical study of ORKA-002 in adult participants with moderate-to-severe HS.

Eligibility Criteria

Inclusion Criteria: 1. Has signs and symptoms of HS for at least 6 months; 2. Has HS lesions present in ≥ 2 distinct anatomic areas, one of which must be at least Hurley Stage II or III; 3. Has a history of inadequate response to systemic antibiotic treatment for HS, exhibited recurrence of HS symptoms after discontinuation of systemic antibiotics for HS, demonstrated intolerance to systemic antibiotics for HS, or has a contraindication to systemic antibiotics for HS Exclusion Criteria: 1. Presence of any other active skin disease or condition that may interfere with the assessment of HS; 2. Diagnosis or suspected diagnosis of autoimmune diseases or inflammatory conditions other than HS

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07783542). StuddyBuddy aggregates publicly available trial information.