Overview

DMT310-001 Topical in the Treatment of Acne Vulgaris

Status:
Completed
Trial end date:
2019-01-28
Target enrollment:
0
Participant gender:
All
Summary
The objective is to evaluate the tolerability, safety, and efficacy of DMT310 topical powder mixed with diluent in male and female patients with moderate to severe facial acne vulgaris.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Dermata Therapeutics
Treatments:
Hydrogen Peroxide
Criteria
Inclusion Criteria:

- Patient is male or non-pregnant female at least 18 years of age.

- Clinical diagnosis of moderate to severe acne vulgaris as determined by:

Investigator's Global Assessment (IGA) at Randomization Patient has at least 20 but not
more than 50 inflammatory lesions on the face Patient has at least 20 but not more than 100
noninflammatory lesions on the face

- Patient is willing to apply the Investigational Product as directed

- Patient is willing and able to comply with the protocol

Exclusion Criteria:

- Patient is pregnant or planning to become pregnant

- Patient is taking a topical therapy on the face which may affect the patient's acne