ATI-502 Topical Solution for the Treatment of Alopecia Areata (AA), Alopecia Universalis (AU) and Alopecia Totalis (AT)

NCT ID: NCT03759340

Last Updated: 2020-10-06

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 56 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-01-15
• Study Completion Date: 2019-09-11

Brief Summary

This is an open label study of ATI-502 Topical Solution for the treatment of AA, AU, and AT with the following goals:

• To assess the safety, tolerability, and efficacy of ATI-502 Topical Solution in subjects with AA, AU or AT following 24 weeks of treatment with ATI-501 Oral Suspension or Placebo Suspension.
• To assess the ability of ATI-502 Topical Solution to maintain or improve hair regrowth in subjects previously treated with ATI-501 Oral Suspension or Placebo Suspension.

Detailed Description

This Phase 2, multicenter, open-label study will evaluate the safety, tolerability, efficacy, and durability of efficacy of ATI-502 Topical Solution, 0.46% for the treatment of alopecia areata (AA), alopecia universalis (AU) and alopecia totalis (AT) in adult subjects who completed 24 weeks of treatment with ATI-501 Oral Suspension or Placebo Suspension.

Subjects who complete 24 weeks of active treatment with ATI-501 Oral Suspension or Placebo Suspension in study ATI-501-AUAT-201 will be assessed for eligibility to enter the study. At Visit 9 in study ATI-501-AUAT-201, subjects who did not experience any adverse events (AEs), serious adverse events (SAEs), or tolerability issues that met study discontinuation criteria in study ATI-501-AUAT-201 and who in the opinion of the investigator are capable of re-growing or maintaining scalp hair and meet the entry criteria are eligible to enroll in this open-label study.

Enrolled subjects will apply ATI-502 Topical Solution, 0.46% BID to the entire scalp and if applicable, the eyebrow(s) and return for safety and efficacy assessments as detailed in the Schedule of Assessments (Table 3). Assessment of response to treatment will be performed at Week 4, Week 8, Week 16, Week 24, and post-treatment Week 28. Safety and tolerability will be evaluated at each study visit by assessment of adverse events, clinical laboratory tests, and vital signs, and at Week 24, and physical examination findings

Conditions

Alopecia Areata; Alopecia Universalis; Alopecia Totalis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

ATI 502 0.46% Topical Solution

Subjects will apply ATI-502 Topical Solution, 0.46% twice-daily for 24 weeks followed by a 4-week post-treatment follow up period.

Group Type: EXPERIMENTAL

ATI 502 0.46% Topical Solution

Intervention Type: DRUG

apply ATI-502 Topical Solution, 0.46% Twice a day (BID) to the entire scalp and if applicable, the eyebrow(s)

Interventions

ATI 502 0.46% Topical Solution

apply ATI-502 Topical Solution, 0.46% Twice a day (BID) to the entire scalp and if applicable, the eyebrow(s)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subjects must meet the following criteria to be eligible for participation in the study:

1. Subject must be able to comprehend and willing to sign the Informed Consent Form (ICF).

2. Male or non-pregnant, non-nursing female ≥ 18 years old at the time of informed consent.

3. Subject has completed 24 weeks of treatment and the assessments for Visit 9 in study ATI-501-AUAT-201.

4. Subject has not experienced any AEs, SAEs or tolerability issues that met study discontinuation criteria in ATI-501-AUAT-201.

5. Subject is capable of regrowing scalp hair or maintaining prior scalp hair regrowth from ATI-501-AUAT-201 in the opinion of the investigator.

6. If a woman of childbearing potential (WOCBP), must have a negative urine pregnancy test at Visit 1 and agree to: use a highly effective method of birth control for the duration of the study; not be planning a pregnancy during the study duration and use contraception for 30 days after last application of study medication. (Refer to Section 8.4).

7. Be in good general health and free of any known disease state or physical condition which, in the investigator's opinion, might impair evaluation of the subject or which might expose the subject to an unacceptable risk by study participation.

8. Be willing to maintain the same general hair style throughout the study period. Subjects who shave their scalp must be willing to refrain from shaving their scalp for at least one week or longer prior to each study visit, as determined by the investigator based on visible scalp hair growth. Hair trimming outside the treatment areas to maintain the current hair style is permitted.

9. Be willing and able to follow all study instructions and to attend all study visits.

10. Sexually active male subjects must agree to use a barrier method of contraception from the first application of study medication to at least 30 days after the last application of study medication.

Exclusion Criteria

• Subjects are excluded from this study if any 1 or more of the following criteria is met:

1. Any study medication discontinuation criteria are met during participation in study ATI-501-AUAT-201.

2. Females who are nursing, pregnant, or planning to become pregnant for the duration of the study and up to 30 days after the last application of study medication.

3. The presence of a permanent or difficult to remove hairpiece or wig that will, in the opinion of the investigator, interfere with study assessments if not removed at each visit.

4. Sensitivity to any of the ingredients in the study medications.

5. Unwillingness to refrain from weaves, hair extensions, or shaving of the scalp for at least one week or longer prior to each study visit, as determined by the investigator based on visible scalp hair growth the duration of the study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Aclaris Therapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Aclaris Investigator Site

Boynton Beach, Florida, United States

Aclaris Investigator Site

Snellville, Georgia, United States

Aclaris Investigator Site

Clinton Township, Michigan, United States

Aclaris Investigator SIte

Detroit, Michigan, United States

Aclaris Investigator Site

Fridley, Minnesota, United States

Aclaris Investigator Site

Minneapolis, Minnesota, United States

Aclaris Investigator Site

Saint Joseph, Missouri, United States

Aclaris Investigator Site

Omaha, Nebraska, United States

Aclaris Investigator Site

Las Vegas, Nevada, United States

Aclaris Investigator Site

New York, New York, United States

Aclaris Investigator Site

Rochester, New York, United States

Aclaris Investigator Site

Portland, Oregon, United States

Aclaris Investigator Site

Greenville, South Carolina, United States

Aclaris Investigator Site

Knoxville, Tennessee, United States

Aclaris Investigational Site

Nashville, Tennessee, United States

Aclaris Investigational Site

Austin, Texas, United States

Aclaris Investigator Site

Houston, Texas, United States

Aclaris Investigator Site

Lynchburg, Virginia, United States

Aclaris Investigator Site

Rogers, Arkansas, United States

Aclaris Investigator Site

Denver, Colorado, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

ATI-502-AA-203

Identifier Type: -

Identifier Source: org_study_id