A Study to Evaluate RIST4721 in Hidradenitis Suppurativa (HS)
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Hidradenitis Suppurativa
In brief
A Randomized, Double-blinded, Placebo-controlled, Phase 2a Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Hidradenitis Suppurativa
Key facts
- Study ID
- NCT05348681
- Run by
- Aristea Therapeutics, Inc.
- People needed
- 25
- Starts
- 2022-07-18
- Expected to finish
- 2023-02-28
- Last updated by the study team
- 2023-06-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of HS for at least 1 year prior to screening
- HS lesions must be present in at least 2 distinct anatomic areas
- A total AN count (sum of abscesses and inflammatory nodules) > 6 across all anatomical sites at both the screening and baseline visits
- Willing to use contraception for the duration of the study
You may not qualify if…
- Presence of other skin conditions which may interfere with study assessments
- Presence of active, chronic or latent bacterial, viral, fungal mycobacterial infection (including latent TB) or history of infection within 4 weeks of screening
- Body Mass Index (BMI) >48kg/m2
- Breastfeeding or pregnant
Where it is running
- Cahaba Dermatology & Skin Center — Birmingham, Alabama, United States
- Investigate MD, LLC — Scottsdale, Arizona, United States
- USC IDS Pharmacy — Los Angeles, California, United States
- Florida Academic Centers Research and Education, LLC — Coral Gables, Florida, United States
- ForCare Clinical Research — Tampa, Florida, United States
- The Indiana Clinical Trials Center, P.C. — Plainfield, Indiana, United States
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
- Wright State Physicians — Fairborn, Ohio, United States
- Progressive Clinical Research — San Antonio, Texas, United States
- Virginia Clinical Research, Inc. — Norfolk, Virginia, United States
- Enverus Medical Research — Surrey, British Columbia, Canada
- SKiN Health — Cobourg, Ontario, Canada
Full record on ClinicalTrials.gov
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