DMT310-005 Topical in the Treatment of Acne Rosacea
Status unconfirmed · Phase 2 · Has a placebo group
Conditions studied: Acne Rosacea
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 rosacea.
Key facts
- Study ID
- NCT05108025
- Run by
- Dermata Therapeutics
- People needed
- 180
- Starts
- 2021-11-15
- Expected to finish
- 2022-12-01
- Last updated by the study team
- 2022-12-08
Who can join
Age: 18 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 papulopustular acne rosacea as determined by:
- Investigator's Global Assessment (IGA) at Randomization score of 3 or 4. Patient has at least 15 inflammatory 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 rosacea
Where it is running
- Dermata Investigational Site — Austin, Texas, United States
Full record on ClinicalTrials.gov
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