A Randomized, Double-blinded, Placebo-controlled, Phase 2a Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects With Hidradenitis Suppurativa

  • End date
    Jun 15, 2023
  • participants needed
  • sponsor
    Aristea Therapeutics, Inc.
Updated on 17 September 2022


A Randomized, Double-blinded, Placebo-controlled, Phase 2a Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Hidradenitis Suppurativa

Condition Hidradenitis Suppurativa
Treatment Placebo, RIST4721
Clinical Study IdentifierNCT05348681
SponsorAristea Therapeutics, Inc.
Last Modified on17 September 2022


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Inclusion Criteria

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

Exclusion Criteria

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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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