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DMT310-001 Topical in the Treatment of Acne Vulgaris

NCT03536637 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 121

Last updated 2020-07-22

No results posted yet for this study

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.

Conditions

  • Acne Vulgaris

Interventions

DRUG

DMT310

Topical Powder

DRUG

Hydrogen Peroxide

Liquid Diluent

DRUG

Placebo

Placebo Topical Powder

Sponsors & Collaborators

  • Dermata Therapeutics

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
FACTORIAL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-22
Primary Completion
2018-12-30
Completion
2019-01-28
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03536637 on ClinicalTrials.gov