Study of EQ101 in Adult Subjects With Moderate to Severe Alopecia Areata

Alopecia Areata Clinical Trial

Official title:

An Open-label, Phase 2 Study to Assess the Safety and Efficacy of EQ101 in Adult Subjects With Moderate to Severe Alopecia Areata

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05589610
• Other study ID #: EQ101-104-01
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: December 19, 2022
• Est. completion date: April 2024

Study information

• Verified date: December 2023
• Source: Equillium
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the safety, PK, and PD of EQ101 as well as measure the efficacy of EQ101 at Week 24 compared to Baseline in adult subjects with moderate to severe AA. The study consists of 3 phases: a screening phase of up to 5 weeks, a treatment phase of 24 weeks, and a follow-up phase of 4 weeks. Study drug will be administered via intravenous (IV) push weekly.

Description:

This is a multicentre, Phase 2, open-label PoC study of EQ101 in adult subjects with at least 35% scalp hair loss due to AA. Approximately, 30 subjects will be enrolled in the study. During the 24-week treatment period, subjects will be dosed once weekly with EQ101 2 mg/kg IV. Subjects then will be followed up for an additional 4 weeks. The maximum duration of study participation will be approximately 33 weeks. Eligible subjects must be between the ages of 18 and 60 years, have a clinical diagnosis of AA with a scalp hair loss of ≥ 35% at Screening and Baseline. Approximately 25% of subjects with 35% to < 50% scalp hair loss and approximately 25% may have AT and/or AU. In addition, each subject's current hair loss episode must have lasted at least 6 months but not more than 7 years and there can be no appreciable improvement in terminal hair regrowth within 6 months of Baseline. Safety, efficacy, PK, and PD assessments will be made during the study. Safety assessments will include AEs (i.e., type, severity, frequency, seriousness, causality) and clinical safety lab results. Efficacy measurements will include Clinical Investigator assessments (e.g., SALT, ClinRO for eyebrows (EB), eyelashes (EL), and body hair changes) and assessments made by study subjects (e.g., Scalp Hair Assessment PRO, and PRO measures for EB, EL, and body hair changes).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: April 2024
• Est. primary completion date: March 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Key Inclusion Criteria:

1.Subjects have AA, meeting all of the following criteria:

1. Clinical diagnosis of AA with no other aetiology of hair loss ;

2. At least 35% scalp hair loss, as defined by a SALT score = 35, at Screening and Baseline. Approximately 25% of subjects with 35% to <50% scalp hair loss and 25% may have AT/AU.

3. Current episode of hair loss lasting > 6 months to < 7 yrs at time of Screening; and

4. No appreciable change in terminal hair regrowth within 6 months of the baseline visit.

Key Exclusion Criteria:

1. Known history of, or currently experiencing, male pattern androgenetic alopecia or female pattern hair loss

2. History of scalp hair transplantation.

3. Other scalp disease that may impact AA assessment or require topical treatment

4. Unwilling to maintain a consistent hair style, including shampoo and hair products, and to refrain from weaves or extensions throughout the course of the study, or shaving of scalp.

5. Use of adhesive or difficult to remove hairpiece or wigs during the study

6. Have undergone significant trauma or major surgery within 8 weeks of the first dose of study drug or considered in imminent need for surgery or with elective surgery scheduled to occur during the study.

7. Participation in other clinical studies involving investigational drug(s) within 4 weeks prior to the baseline visit.

8. Treatment with an oral JAK inhibitor within 6 months prior to the baseline visit.

9. Have previously been treated with an oral JAK inhibitor for AA for at least 12 weeks without achieving at least a 25% improvement in SALT score.

10. Have been treated with any cell-depleting agents including but not limited to rituximab: within 6 months of the baseline visit, or 5 half-lives (if known), or until lymphocyte count returns to normal, whichever is longer.

11. Have been treated with any biologics within 12 weeks or 5 half-lives of the baseline visit, whichever is longer.

12. Have been treated with any oral immune suppressants within 8 weeks of the baseline visit.

13. Have received intralesional injections of corticosteroid or platelet-rich plasma (PRP) in the scalp within 6 weeks of the baseline visit.

14. Have used phototherapy, contact sensitisers, contact irritants, or cryotherapy within 4 weeks of the baseline visit.

15. Have used topical treatments applied to the scalp, eyebrows, or eyelashes (e.g., corticosteroid cream; JAK inhibitors; medicated shampoo; minoxidil (Rogaine); or herbal hair care that could affect AA) within 4 weeks of the baseline visit.

16. Have current or recent history of clinically significant severe, progressive, or uncontrolled renal, hepatic, haematological, gastrointestinal, metabolic, endocrine, pulmonary, cardiovascular, psychiatric, immunologic/rheumatologic or neurologic disease; or have any other severe acute or chronic medical or psychiatric condition or laboratory abnormality

17. Have a known immunodeficiency disorder.

18. History of solid organ or haematological transplantation.

19. History of a lymphoproliferative disease or malignancy, other than adequately treated non-melanoma skin cancer or cervical carcinoma with no evidence of recurrence.

20. Have active acute or chronic infection

21. Abnormalities in clinical laboratory tests at Screening:

1. Absolute neutrophil count (ANC) <1.0 × 109/L.

2. Liver function tests ( ALT and AST) >3 x ULN.

3. Total bilirubin >1.5 times ULN (unless isolated Gilbert's syndrome)

4. Serum creatinine >1.5 ULN.

Related Conditions & MeSH terms

• Alopecia
• Alopecia Areata
• Alopecia Totalis
• Alopecia Universalis

Intervention

Drug:
• EQ101
EQ101, 2 mg/kg, once weekly dosing, for a total of 24 doses

Locations

Country	Name	City	State
Australia	Sinclair Dermatology	East Melbourne
Australia	Fremantle Dermatology	Fremantle
Australia	Premier Specialists	Kogarah
Australia	Veracity Clinical Research	Woolloongabba
New Zealand	Optimal Clinical Trials Limited	Auckland

Sponsors (2)

Lead Sponsor	Collaborator
Equillium	Equillium AUS Pty Ltd

Countries where clinical trial is conducted

Australia,  New Zealand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Treatment Emergent Adverse Events	Number of participants with treatment-related adverse events as assessed by the Common Terminology Criteria for Adverse Events (CTCAE)	Week 28
Secondary	The efficacy of EQ101 in adult subjects with moderate to severe Alopecia	Percent change in SALT score	Week 24
Secondary	To characterize the pharmacokinetics (PK) of EQ101	To characterize the pharmacokinetics (PK) of EQ101 by plasma concentrations	Week 24
Secondary	To characterize the pharmacodynamics (PD) of EQ101	Percent change in target engagement	Week 24

External Links

•   Company website