Overview

Profiling the Skin Microbiome in Response to Altreno in Acne Patients

Status:
Recruiting
Trial end date:
2022-12-31
Target enrollment:
0
Participant gender:
All
Summary
The study objective is to characterize the shift in the diversity and abundance of the skin microbial community at baseline and in response to Altreno monotherapy as compared to benzoyl peroxide (BPO) 2.5% leave-on gel monotherapy in acne patients.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Beth Israel Deaconess Medical Center
Collaborator:
Ortho Dermatologics
Treatments:
Benzoyl Peroxide
Criteria
Inclusion Criteria:

- A confirmed diagnosis of acne that warrants initiating topical medications.

- Denies use of any prescribed systemic acne treatments in the past 30 days.

- Denies use of any prescribed topical medications in the past 30 days.

- Denies use of any OTC topical acne medications in the past 14 days.

- Denies use of any emollients in the past 24 hours (if feasible).

- Denies bathing or facial washing in the past 12 hours (if feasible).

- Willingness to adhere to the recommended topical regimen during the duration of the
study.

Exclusion Criteria:

- Women who are pregnant, breastfeeding, or planning to get pregnant during the study.

- Use of any investigational drug(s) in the past 3 months.