Phase 2 Alopecia Areata Trial, Recruiting NCT07317544 Sponsor: Absci Pty Ltd. Condition: Alopecia Areata
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Phase 2 Alopecia Areata Trial, Recruiting

NCT07317544
Recruiting Phase 2 🇦🇺 Australian site

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 must be generally healthy, based on a review of your medical history, a physical exam, and a heart tracing test (ECG)
  • Your blood tests, urine tests, and clotting tests must all come back within normal ranges
  • Your body mass index (BMI) must be between 18 and 32, and you must weigh more than 60 kg (about 132 lbs)
  • Both men and women must be willing to avoid pregnancy for the entire duration of the trial
  • You must be able to and willing to sign a consent form agreeing to take part
  • You must have no signs or symptoms of tuberculosis (TB), either active or hidden

For people joining with hair loss (AGA) specifically:

  • You must have a confirmed diagnosis of a specific pattern of hair loss, rated on a recognised medical scale (Norwood-Hamilton Scale III vertex to V for men, or Ludwig Scale I-3, I-4, II-1, or II-2 for postmenopausal women)
  • You must be willing to have the hair in the study area clipped for analysis and avoid using colour or pigment products on your scalp
  • You must be willing to keep roughly the same hair length at every study visit
  • For postmenopausal women: your hair loss must have been present for at least 12 months, with no sudden or rapid worsening in the 6 months before joining

Who may not be able to join:

  • You have a history of cancer, unless it was basal cell skin cancer or a cervical condition that was fully treated with no return for at least 90 days before the trial
  • You have a history of liver disease or abnormal liver function test results
  • Your blood pressure or heart rate falls outside a certain safe range at screening (confirm with trial site)
  • You test positive for HIV, hepatitis B, or hepatitis C
  • You have recently donated blood
  • You have a significant psychiatric (mental health) condition
  • You are pregnant, breastfeeding, or planning to become pregnant during the study
  • You have a history of postnatal depression, mood changes around menopause, or symptoms related to estrogen withdrawal

For people joining with hair loss (AGA) specifically:

  • You have used certain hair loss treatments recently, including minoxidil (topical within 3 months, oral within 6 months), finasteride within 6 months, or dutasteride within 12 months before screening
  • You have used certain weight-loss or diabetes medications (such as semaglutide or tirzepatide) within 3 months before screening
  • You have had a hair transplant or major scalp procedure, or have one planned during the study
  • You have used hair extensions, wigs, weaves, or similar artificial hair products within 30 days before screening or during the study
  • You have a significant skin condition affecting your scalp that could interfere with hair assessments

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

Phone: +1.860.857.4560

Australian sites

Momentum Darlinghurst, Sydney, New South Wales
Nucleus Network Brisbane, Brisbane, Queensland
+61 (07) 3707 2720
Sinclair Dermatology, Melbourne, Victoria
Nucleus Network, Melbourne, Victoria

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
Sponsor
Absci Pty Ltd.
Registry
ClinicalTrials.gov
Start date
3 December 2025
Est. completion
1 July 2028

Where this trial is recruiting

🇦🇺 Australia

4 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Incidence rate of treatment-related adverse events

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