Phase 2 Alopecia Areata Trial, Completed NCT05589610 Sponsor: Equillium Condition: Alopecia Areata
Back to Alopecia Areata

Trial results

AI generated results 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

According to the results reported on ClinicalTrials.gov, this trial looked at a treatment called EQ101 in people with moderate to severe alopecia (significant hair loss). A total of 36 people started the trial, 30 people completed it, and 6 did not finish. The trial was measuring how many participants experienced side effects or unwanted health events that arose during treatment (called "treatment emergent adverse events"), as well as several other things including changes in hair loss scores, how the body processed the drug, and how the drug interacted with its biological target in the body. The reported data shows that out of 36 participants, 27 experienced at least one treatment-related adverse event (an unwanted health occurrence that appeared during the treatment period). This was the primary — or main — thing the trial was tracking. For the remaining outcome measures — including changes in hair loss scores, how the body absorbed and processed EQ101, and the drug's interaction with its biological target — the data was not reported on ClinicalTrials.gov, so no numbers are available for those results. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 2 Alopecia Areata Trial, Completed

NCT05589610
Completed 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 have been diagnosed with alopecia areata (AA) as the only known reason for your hair loss
  • You have lost at least 35% of your scalp hair, as measured by a standard scoring tool called SALT, at the time of your screening and baseline visits
  • Your current episode of hair loss has been going on for more than 6 months but less than 7 years at the time of screening
  • There has been no noticeable new hair regrowth in the 6 months before your baseline visit

Who may not be able to join:

  • You have, or have had, male or female pattern baldness (the common inherited type of hair loss)
  • You have had a hair transplant on your scalp
  • You have another scalp condition that could affect how your hair loss is measured or that needs treatment applied to the scalp
  • You are unwilling to keep a consistent hairstyle, use the same shampoo and hair products throughout the study, or avoid weaves, extensions, or shaving your scalp
  • You plan to use a glued-on or hard-to-remove hairpiece or wig during the study
  • You have had a major surgery or serious injury within the past 8 weeks, have surgery coming up soon, or have planned surgery scheduled during the study
  • You have taken part in another clinical trial involving an experimental drug within the past 4 weeks before your baseline visit
  • You have taken an oral JAK inhibitor medication within the past 6 months before your baseline visit
  • You have previously taken an oral JAK inhibitor for alopecia areata for 12 weeks or more without seeing at least a 25% improvement in your hair loss score
  • You have received a cell-depleting treatment (such as rituximab) within the past 6 months, or until your immune cell levels return to normal, whichever is longer
  • You have received a biologic medication within the past 12 weeks, or within a specific washout period based on the medication, whichever is longer
  • You have taken oral immune-suppressing medications within the past 8 weeks before your baseline visit
  • You have had steroid injections or platelet-rich plasma (PRP) injections into your scalp within the past 6 weeks
  • You have used light therapy, certain skin sensitising or irritating treatments, or cryotherapy (freezing treatment) within the past 4 weeks
  • You have used any topical treatments on your scalp, eyebrows, or eyelashes (such as steroid creams, JAK inhibitor creams, medicated shampoos, minoxidil, or herbal hair products that could affect hair loss) within the past 4 weeks
  • You have a significant, ongoing, or poorly controlled condition affecting your kidneys, liver, blood, digestive system, hormones, lungs, heart, mental health, immune system, or nervous system
  • You have a known condition that weakens your immune system
  • You have had a solid organ or bone marrow/blood cell transplant
  • You have a history of lymphoma or other cancer, except for certain treated skin cancers or cervical cancer with no signs of return
  • You currently have, or recently had, a significant infection (either short-term or ongoing)
  • Certain blood test results at screening are outside acceptable ranges, including low levels of a type of white blood cell, raised liver enzyme levels, raised bilirubin levels, or raised creatinine (kidney function) levels (confirm exact thresholds with trial site)

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

Australian sites

Sinclair Dermatology, East Melbourne,
Fremantle Dermatology, Fremantle,
Premier Specialists, Kogarah,
Veracity Clinical Research, Woolloongabba,

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
Completed
Phase
Phase 2
Sponsor
Equillium
Registry
ClinicalTrials.gov
Start date
19 December 2022
Est. completion
26 March 2024

Where this trial is recruiting

🇦🇺 Australia 🇳🇿 New Zealand

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

Primary endpoints

Number of Treatment Emergent 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