DMT310-001 Topical in the Treatment of Acne Vulgaris

Completed · Phase 2 · Has a placebo group

Conditions studied: Acne Vulgaris

In brief

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.

Key facts

Study ID

NCT03536637

Run by

Dermata Therapeutics

People needed

121

Starts

2018-05-22

Expected to finish

2019-01-28

Last updated by the study team

2020-07-22

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• Patient is pregnant or planning to become pregnant
• Patient is taking a topical therapy on the face which may affect the patient's acne

Where it is running

• Dermata Investigational Site — San Diego, California, United States
• Dermata Investigational Site — Saint Joseph, Missouri, United States
• Dermata Investigational Site — Henderson, Nevada, United States
• Dermata Investigational Site — Albuquerque, New Mexico, United States
• Dermata Investigational Site — High Point, North Carolina, United States
• Dermata Investigational Site — Tennessee City, Tennessee, United States
• Dermata Investigational Site — Austin, Texas, United States
• Dermata Investigational Site — College Station, Texas, United States
• Dermata Investigational Site — Katy, Texas, United States

Full record on ClinicalTrials.gov

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