Recruiting
Phase 2

Alopecia Areata

Sponsor:

University of Minnesota

Code:

NCT06747611

Conditions

Alopecia Areata

Alopecia Totalis

Alopecia Universalis

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Vancomycin, Neomycin and MTT capsules

Placebo capsules

Study Details

Brief summary:

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

Alopecia Areata

Alopecia Totalis

Alopecia Universalis

Study ID

NCT06747611

Start date

Aug 21, 2025

Status verified date

Jun, 2026

Completion date

Mar 15, 2028

Anticipated

Primary completion date

Mar 15, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Patients 18 to 75 years of age with moderate to severe alopecia areata (SALT score >30%).
  • Patients with a diagnosis of patch type alopecia areata, totalis, or universalis..
  • Duration of hair loss >=3 months..
  • No evidence of active, ongoing regrowth present at baseline.
  • Females of childbearing potential must have a negative urine or serum pregnancy test at screening and immediately prior to MTT.
  • Females of childbearing potential must agree to use an effective form of contraception from 14 days prior to study antibiotics through at least 30 days after MTT. Acceptable forms of contraception include oral or intramuscular contraceptives, intrauterine devices, surgical sterilization.
  • Participants are not enrolled in another clinical study.
  • If undergoing treatment with a JAK inhibitor, participant is willing to discontinue treatment for 1 month prior to enrollment and throughout the duration of the study.

Exclusion Criteria:

  • Active gastrointestinal infection at time of enrollment.
  • Having been administered antibiotics in the last 48 hours.
  • Patients will be eligible to enroll if antibiotic therapy is discontinued for at minimum 48 hours prior to treatment..
  • Requires continued antibiotic use
  • Allergy to study antibiotics (vancomycin, neomycin).
  • Known or suspected severe gastrointestinal dysmotility disorder, e.g., gastroparesis, pseudo-obstruction, scleroderma with gastrointestinal involvement
  • Ileus or small bowel obstruction.
  • Major gastrointestinal surgery (e.g., significant bowel resection) within 3 months before enrollment. This does not include appendectomy or cholecystectomy.
  • History of total colectomy.
  • Concurrent intensive induction chemotherapy, radiation therapy or biological treatment for active malignancy.
  • Unable or unwilling to comply with protocol requirements.
  • Expected life expectancy \< 6 months.
  • Previous MTT or microbiome-based products at any time excluding this study.
  • History of severe anaphylactic or anaphylactoid food allergy.
  • Solid organ transplant recipients 90 days post-transplant or on active treatment for rejection.
  • A condition that would jeopardize the safety or rights of the subject, would make it unlikely for the subject to complete the study, or would confound the results of the study.
  • History of or existing skin diseases affecting the scalp such as psoriasis or seborrheic dermatitis and patients with evidence of infection or skin cancer in the treated areas.
  • Patients in whom the diagnosis of alopecia areata is questionable.
  • Patients in whom regrowth is present/evident at baseline in the areas to be treated.
  • Patients with active medical conditions or malignancies (except adequately treated basal or squamous cell carcinoma of the skin) which in the opinion of the investigator would increase the risks associated with study participation, including patients with a history of recurrent infections.
  • Patients unwilling or unable to discontinue treatments known to affect hair regrowth in alopecia areata.
  • Patients who have been treated with intralesional steroids, systemic steroids, anthralin, squaric acid, DPCP (diphenylcycloprophenone), protopic, minoxidil, JAK inhibitors or other medication which in the opinion of the investigator may affect hair regrowth, within one month of the baseline visit..
  • Patients determined by the investigator to have extreme diets..
  • Pregnant and breastfeeding females..

Study Design

Enrollment

40 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Alopecia Areata study group

randomized to receive antibiotics and MTT oral capsule

placebo comparator: Alopecia Areata control group

randomized to receive placebo antibiotics and placebo MTT oral capsule

Interventions

Vancomycin, Neomycin and MTT capsules

patients will take 2 capsules per day for 14 days. These patients will then be clinically followed for a period of 24 weeks.

Placebo capsules

patients will take 2 capsules per day for 14 days. These patients will then be clinically followed for a period of 24 weeks.

Primary outcome measure

  • Engraftment [ Time Frame: Week 8 ]

Central Contacts and Locations

Central contacts

Thomas Pritchard

612-626-0249pritc204@umn.edu

Locations

University of Minnesota

Recruiting

Minneapolis, Minnesota, United States, 55455

Contacts

Thomas Pritchard

612-626-0249pritc204@umn.edu

More Information

Sponsor

University of Minnesota

Last update posted

Jun 26, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-27. This information was provided to ClinicalTrials.gov by University of Minnesota on 2026-06-26. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.