Capsule Microbiota Transplant Therapy for Hidradenitis Suppurativa

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Minnesota

About this trial

HS is relatively common in the United States with a prevalence of 0.1-1.0%. 1 HS has a dramatic impact on quality of life, significantly more so than other chronic skin diseases, such as psoriasis or atopic dermatitis (AD). HS also has a large economic impact, due to frequent emergency department and inpatient care utilization, and re-hospitalization rates similar to congestive heart failure. Unfortunately, few treatment options are effective. There are currently three FDA-approved treatments for HS, including adalimumab, secukinumab, and bimekizumab, each with only 40- 60% respond to treatment and over 50% lose response within one year . The overarching goal of this pilot study is to investigate the central hypothesis that oral microbiota transplant therapy(MTT) alters the gut microbiome in patients with Hidradenitis Suppurativa (HS), influencing cutaneous microbiota via systemically absorbed gut-derived metabolites.

Eligibility criteria

Qualifiers

Able and willing to provide informed consent

English speaking

Age >= 18years of age

Diagnosis of hidradenitis suppurativa by a dermatologist

Disqualifiers

Non-English speaking

Refusal or inability to provide informed consent

Planning on moving within 6 months from start of study

Allergy to neomycin or vancomycin

Trial design

Treatments tested in this trial

  • Fecal Microbiota - lyophilized
  • Placebo drug

Treatment groups

16 Participants
are divided into 2 treatment groups

Sponsors and collaborators