A Phase 2b Study to Evaluate Rezpegaldesleukin (Rezpeg) in the Treatment of Severe to Very Severe Alopecia Areata in Adult Patients (Rezolve AA)

Inclusion Criteria:

• Adults who are at least 18 years and ≤60 years for males (≤70 years of age forfemales) old at the time of informed consent

• Diagnosis of Alopecia Areata (AA) severity at screening and baseline:

1. severe to very severe AA (≥ 50% scalp involvement) as measured using the SALTscore

2. Documented history over 6 months with no spontaneous improvement prior tobaseline

3. Current episode of severe to very severe AA of less than 8 years

• Women of childbearing potential (WOCBP) must have a negative pregnancy test atscreening and baseline.

• While on investigational product and for at least 30 days after taking the last doseof investigational product (IP), WOCBP who engage in activity in which conception ispossible must use approved highly effective contraceptive method(s). For malepatient with partner that is WOCBP in which conception is possible, male patientmust agree to use approved highly effective contraceptive method(s).

• Able to complete patient questionnaires

• Able and willing to comply with requested study visits and procedures

• Able and willing to provide written informed consent

• Able to communicate, read and/or understand the local language

Exclusion Criteria:

• Men and women (of reproductive potential) unwilling to use birth control and womenwho are pregnant or breastfeeding.

• Patient has primarily "diffuse" type AA (characterized by diffuse hair shedding).

• Presence of another form of alopecia.

• Prior use of any of the following treatments:

1. aldesleukin

2. investigational IL-2 analog

3. oral Janus kinase (JAK) inhibitor for any indication, including, but notlimited to, baricitinib, upadacitinib, abrocitinib, tofacitinib, andruxolitinib, whether marketed or investigational

4. systemic immune-modulating biologic therapy (including, but not limited to,dupilumab, tralokinumab, lebrikizumab, nemolizumab, rocatinlimab, rituximab,ocrelizumab, ofatumumab, belimumab, daxdilimab, etc.) whether marketed orinvestigational

• History of cancer or lymphoproliferative disease within 5 years prior to Day 1.Note: Patients with successfully treated nonmetastatic cutaneous squamous cell orbasal cell carcinoma with no evidence of metastatic disease for 3 years and/orlocalized carcinoma in situ of the cervix with no evidence of recurrence within the 3 years prior to Day 1 are not to be excluded.

• Current infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV),or hepatitis C virus (HCV) at screening.

• Other skin conditions that would interfere with study assessments of AA