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Completed Phase 2 Interventional

DMT310-001 Topical in the Treatment of Acne Vulgaris

ClinicalTrials.gov ID: NCT03536637

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT03536637. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 4:57 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study of Tolerability, Safety, And Efficacy, of DMT310 In Patients With Acne Vulgaris

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03536637
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dermata Therapeutics
Industry
Enrollment
121 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 22, 2018 (Actual)
Primary completion
Dec 30, 2018 (Actual)
Completion
Jan 28, 2019 (Actual)
Last update posted
Jul 22, 2020

2018 – 2019

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Dermata Investigational Site San Diego California 92123 —
Dermata Investigational Site Saint Joseph Missouri 64506 —
Dermata Investigational Site Henderson Nevada 89148 —
Dermata Investigational Site Albuquerque New Mexico 87106 —
Dermata Investigational Site High Point North Carolina 27262 —
Dermata Investigational Site Tennessee City Tennessee 37215 —
Dermata Investigational Site Austin Texas 78759 —
Dermata Investigational Site College Station Texas 77802 —
Dermata Investigational Site Katy Texas 77494 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03536637, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 22, 2020 · Synced Nov 12, 2026

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