Status:
TERMINATED
ATI-502 Topical Solution for the Treatment of Alopecia Areata (AA), Alopecia Universalis (AU) and Alopecia Totalis (AT)
Lead Sponsor:
Aclaris Therapeutics, Inc.
Conditions:
Alopecia Areata
Alopecia Universalis
Eligibility:
All Genders
18+ years
Phase:
PHASE2
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...
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), a...
Eligibility Criteria
Inclusion
- Subjects must meet the following criteria to be eligible for participation in the study:
- Subject must be able to comprehend and willing to sign the Informed Consent Form (ICF).
- Male or non-pregnant, non-nursing female ≥ 18 years old at the time of informed consent.
- Subject has completed 24 weeks of treatment and the assessments for Visit 9 in study ATI-501-AUAT-201.
- Subject has not experienced any AEs, SAEs or tolerability issues that met study discontinuation criteria in ATI-501-AUAT-201.
- Subject is capable of regrowing scalp hair or maintaining prior scalp hair regrowth from ATI-501-AUAT-201 in the opinion of the investigator.
- 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).
- 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.
- 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.
- Be willing and able to follow all study instructions and to attend all study visits.
- 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
- Subjects are excluded from this study if any 1 or more of the following criteria is met:
- Any study medication discontinuation criteria are met during participation in study ATI-501-AUAT-201.
- 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.
- 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.
- Sensitivity to any of the ingredients in the study medications.
- 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.
Key Trial Info
Start Date :
January 15 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 11 2019
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT03759340
Start Date
January 15 2019
End Date
September 11 2019
Last Update
October 6 2020
Active Locations (20)
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1
Aclaris Investigator Site
Rogers, Arkansas, United States, 72758
2
Aclaris Investigator Site
Denver, Colorado, United States, 80210
3
Aclaris Investigator Site
Boynton Beach, Florida, United States, 33472
4
Aclaris Investigator Site
Snellville, Georgia, United States, 30078