DMT310-009 Topical in the Treatment of Acne Vulgaris

  • STATUS
    Recruiting
  • participants needed
    555
  • sponsor
    Dermata Therapeutics
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Updated on 15 May 2025
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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

Details
Condition Acne Vulgaris
Age 9years or above
Clinical Study IdentifierNCT06090721
SponsorDermata Therapeutics
Last Modified on15 May 2025

Eligibility

 Yes No Not Sure

Inclusion Criteria

Patient sex at birth, male or non-pregnant female at least 9 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
inflammatory lesions and at least 20 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
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