Actively Recruiting
Evaluation of Microbiota Transplant Therapy in Patients With Alopecia Areata
Led by University of Minnesota · Updated on 2025-09-08
40
Participants Needed
1
Research Sites
133 weeks
Total Duration
On this page
Sponsors
U
University of Minnesota
Lead Sponsor
C
Columbia University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Alopecia Areata (AA) is among the most highly prevalent human autoimmune diseases, leading to disfiguring hair loss due to the collapse of immune privilege of the hair follicle and subsequent autoimmune attack. AA affects about 5.3 million people in the United States alone, including males and females across all ethnic groups, with a lifetime risk of 2.1%. Autoimmunity develops against the hair follicle, resulting in non-scarring hair loss that may begin as patches that can coalesce and progress to cover the entire scalp (alopecia totalis) or eventually the entire body (alopecia universalis). In AA, there is no permanent destruction of the hair follicle, and regrowth remains possible. Treatment options for AA include intralesional steroids, topical anthralin, allergic contact dermatitis with diphencyprone (DPCP), dinitrochlorobenzene (DNCB), or squaric acid dibutyl ester (SADBE), and recently janus kinase ( JAK) inhibitors. Despite the recent approval of JAKs for the treatment of extensive alopecia areata, some patients are treatment resistant, suffer relapses, or cannot take an oral immunosuppressive medication. This study will attempt to elucidate the pre-treatment and post treatment skin and gut microbiome composition to determine whether specific bacterial species may correlate with disease or treatment response. To determine the effects of MTT on immune cell composition and activation systemically and locally in the skin, we will analyze major immune cell populations in peripheral blood samples and collect skin biopsies for histopathology and next generation sequencing analyses. Further, to determine if changes in immune cell populations affect the inflammatory response, we will profile inflammatory cytokines. To identify if changes in the gut microbiota influence the metabolic signature in AA, we will also perform untargeted metabolomics in stool gut microbiome samples and in plasma. Altogether, this comprehensive approach aims to identify the pathogenic immunological mechanisms associated with microbiome composition correlated to pre-treatment disease, post-treatment response, and any non-responders to treatment.
CONDITIONS
Official Title
Evaluation of Microbiota Transplant Therapy in Patients With Alopecia Areata
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 75 years with moderate to severe alopecia areata (SALT score >30%)
- Diagnosis of patch type alopecia areata, alopecia totalis, or alopecia universalis
- Hair loss duration of 3 months or longer
- No active hair regrowth at the start of the study
- Females of childbearing potential must have a negative pregnancy test at screening and before treatment
- Females of childbearing potential must agree to use effective contraception from 14 days before antibiotics through 30 days after treatment
- Not enrolled in another clinical study
- If using JAK inhibitors, willing to stop treatment 1 month before and during the study
You will not qualify if you...
- Active gastrointestinal infection at enrollment
- Antibiotic use within 48 hours prior to treatment
- Need for ongoing antibiotic therapy
- Allergy to vancomycin or neomycin
- Severe gastrointestinal motility disorders or bowel obstructions
- Major bowel surgery within 3 months prior (excluding appendectomy or gallbladder removal)
- History of total colectomy
- Receiving intensive chemotherapy, radiation, or biological cancer treatment
- Unable or unwilling to follow study requirements
- Life expectancy less than 6 months
- Prior microbiota transplant or microbiome-based treatments
- Severe food allergies causing anaphylaxis
- Organ transplant recipients less than 90 days post-transplant or on rejection treatment
- Conditions risking safety or study completion
- Other scalp skin diseases or infections in treated areas
- Uncertain alopecia areata diagnosis
- Active hair regrowth in treated areas at baseline
- Active medical conditions or malignancies increasing study risk
- Unwillingness or inability to stop treatments affecting hair regrowth within 1 month before baseline
- Extreme diets as determined by the investigator
- Pregnant or breastfeeding females
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55455
Actively Recruiting
Research Team
J
John Meisenheimer
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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