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.
View full results on ClinicalTrials.gov ↗
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
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.
Contact this trial
Australian sites
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
Where this trial is recruiting
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?
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.