Phase 2 Alopecia Areata Trial, Recruiting NCT06747611 Sponsor: University of Minnesota Condition: Alopecia Areata
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Phase 2 Alopecia Areata Trial, Recruiting

NCT06747611
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 18 and 75 years old and have moderate to severe hair loss from alopecia areata (affecting more than 30% of the scalp).
  • You have been diagnosed with patch-type alopecia areata, alopecia totalis, or alopecia universalis.
  • Your hair loss has been present for at least 3 months.
  • There is no visible new hair regrowth happening at the start of the study.
  • If you are a woman who could become pregnant, you must have a negative pregnancy test before joining.
  • If you are a woman who could become pregnant, you must agree to use an effective form of birth control (such as the pill, an injection, an IUD, or surgical sterilization) starting 14 days before the study antibiotics through at least 30 days after the treatment.
  • You are not currently taking part in another clinical trial.
  • If you are currently taking a JAK inhibitor medication, you are willing to stop taking it for at least 1 month before joining and for the entire length of the study.

Who may not be able to join:

  • You currently have an active infection in your digestive system (stomach or intestines).
  • You have taken antibiotics within the last 48 hours (though you may be eligible if antibiotics have been stopped for at least 48 hours before treatment).
  • You need to continue taking antibiotics on an ongoing basis.
  • You have an allergy to the study antibiotics (vancomycin or neomycin).
  • You have a known serious condition that affects how your digestive system moves food through, such as gastroparesis or certain complications of scleroderma (confirm with trial site).
  • You have a blockage in your small intestine or a condition called ileus (confirm with trial site).
  • You have had major surgery on your digestive tract within the last 3 months (note: appendix or gallbladder removal does not count).
  • You have had your entire colon surgically removed.
  • You are currently receiving intensive chemotherapy, radiation, or biological therapy for cancer.
  • You are unable or unwilling to follow the study's requirements.
  • Your life expectancy is less than 6 months.
  • You have previously received a microbiome transplant treatment (MTT) or any microbiome-based product.
  • You have a history of severe, life-threatening food allergies.
  • You have received a solid organ transplant within the last 90 days or are being treated for organ rejection.
  • You have another condition that could put your safety at risk, make it unlikely you would finish the study, or affect the study results.
  • You have a skin condition affecting your scalp, such as psoriasis or seborrheic dermatitis, or any signs of infection or skin cancer on the scalp.
  • Your alopecia areata diagnosis is uncertain.
  • There is already visible hair regrowth in the areas to be treated at the start of the study.
  • You have an active serious medical condition or cancer (except certain minor treated skin cancers) that the study doctor believes would increase your risk, including a history of frequent infections.
  • You are unwilling or unable to stop using treatments known to affect hair regrowth in alopecia areata.
  • You have used certain hair loss treatments — including steroid injections, steroid tablets, minoxidil, JAK inhibitors, or other related medications — within one month before the start of the study.
  • The study doctor considers your diet to be extreme.
  • You are currently pregnant or breastfeeding.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Maria K Hordinsky, MD, University of Minnesota

Phone: 612-626-0249

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
21 August 2025
Est. completion
15 March 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Engraftment

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov