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

NCT07783542

This study is recruiting at 14 US sites in 11 states, according to its ClinicalTrials.gov record last updated .

Summary

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

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Hidradenitis Suppurativa (HS)

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 to 79 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Oruka Therapeutics, Inc.
Last updated on ClinicalTrials.gov
September 24, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Alabama · 1

  • Oruka Therapeutics Investigative Site · Birmingham, AL

California · 2

  • Oruka Therapeutics Investigative Site · Fountain Valley, CA
  • Oruka Therapeutics Investigative Site · Los Angeles, CA

Connecticut · 1

  • Oruka Therapeutics Investigative Site · Cromwell, CT

Georgia · 1

  • Oruka Therapeutics Investigative Site · Sandy Springs, GA

Illinois · 1

  • Oruka Therapeutics Investigative Site · Chicago, IL

Louisiana · 1

  • Oruka Therapeutics Investigative Site · New Orleans, LA

Michigan · 1

  • Oruka Therapeutics Investigative Site · Canton, MI

Minnesota · 1

  • Oruka Therapeutics Investigative Site · New Brighton, MN

Nebraska · 1

  • Oruka Therapeutics Investigative Site · Omaha, NE

Oregon · 1

  • Oruka Therapeutics Investigative Site · Portland, OR

Texas · 3

  • Oruka Therapeutics Investigative Site · Dallas, TX
  • Oruka Therapeutics Investigative Site · Missouri City, TX
  • Oruka Therapeutics Investigative Site · San Antonio, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.