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DMT210 5%

Phase 2

Acne Rosacea | Small molecule | Dermatology |Dermata Therapeutics, Inc.|Last Updated: Apr 18, 2018

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment107

FDA Designations

No designations recorded

Clinical trial landscape

DMT210 5% · 1 trial · 1 indication

Phase 2 1
NCT03003104DMT210 Topical Gel in the Treatment of Acne RosaceaAcne Rosacea
COMPLETED107 Analytics
PHASE2COMPLETED
DMT210 Topical Gel in the Treatment of Acne Rosacea
Acne RosaceaUnlock trial analytics

Study Endpoints

Primary Endpoints

Efficacy as measured by Inflammatory lesion counts
12 weeks

Inflammatory lesion counts

Efficacy as measured by Investigator Global Assessment (IGA)
12 weeks

Investigator Global Assessment (IGA)

Efficacy as measured by 5-point Clinical Erythema Assessment (CEA)
12 weeks

5-point Clinical Erythema Assessment (CEA)

Efficacy as measured by 5-point Patient Severity Assessment of Erythema (PSA)
12 weeks

5-point Patient Severity Assessment of Erythema (PSA)

Secondary Endpoints

Incidence of adverse events as a measure of safety and tolerability
12 weeks
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Study Design & Arms

AllocationRANDOMIZED
MaskingTRIPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
DMT210 Topical GelEXPERIMENTALDMT210 Topical Gel 5% applied to the face twice daily for 12 weeks
Vehicle ControlPLACEBO_COMPARATORTopical Gel vehicle applied to the face twice daily for 12 weeks

Interventions

NameTypeDescription
DMT210 Topical Gel 5%DRUG -
Vehicle ControlOTHER -
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites9

Inclusion Criteria: * Patient is male or non-pregnant female at least 18 years of age. * Clinical diagnosis of moderate to severe facial rosacea as determined by Investigator's Global Assessment (IGA) at Randomization * Patient has at least ten inflammatory lesions of rosacea on the face at Randomi...

Countries:United States
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Frequently asked questions about DMT210 5%

What is DMT210 5% used for?

DMT210 5% is an investigational small molecule topical gel being studied for the treatment of acne rosacea, a chronic inflammatory skin condition. It is in Phase 2 clinical development and is not yet approved by regulatory authorities.

Who makes DMT210 5%?

DMT210 5% is being developed by Dermata Therapeutics, Inc., a biopharmaceutical company traded on the Nasdaq under the ticker symbol DRMA. The company is focused on developing novel treatments for dermatological conditions.

What phase is DMT210 5% in?

DMT210 5% is in Phase 2 clinical development. It has completed one Phase 2 trial, and it remains an investigational drug, meaning it has not been approved by the FDA or other regulatory agencies for commercial use.

What clinical trials is DMT210 5% in?

DMT210 5% has one completed clinical trial, NCT03003104, titled 'DMT210 Topical Gel in the Treatment of Acne Rosacea.' This was a Phase 2, randomized, double-blind, placebo-controlled study conducted in the United States with 107 participants aged 18 years and older.

How does DMT210 5% work?

The specific molecular target of DMT210 5% has not been disclosed. It is a small molecule topical gel being investigated for its potential to treat acne rosacea, but its mechanism of action is not publicly detailed.