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DMT210 5%

Phase 2

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

DMT210 5% target and mechanism

ModalitySmall molecule

Also known as DMT210 Topical Gel 5%

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

DMT210 5% clinical trials

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%?

DMT210 5% is an investigational small molecule topical gel developed by Dermata Therapeutics, Inc. for the treatment of acne rosacea. It is applied to the skin and is being studied as a dermatology therapy. The drug is in Phase 2 clinical development and has not been approved by the FDA.

What is DMT210 5% used for?

DMT210 5% is being developed for the treatment of acne rosacea, a chronic inflammatory skin condition. Its only completed clinical study enrolled adults with acne rosacea in the United States. The drug remains investigational and is not approved for any indication.

Who makes DMT210 5%?

DMT210 5% is developed by Dermata Therapeutics, Inc., which trades on the Nasdaq under the ticker DRMA. The company is the sponsor of the drug's clinical program in dermatology.

What phase is DMT210 5% in?

DMT210 5% is in Phase 2 clinical development. One Phase 2 trial has been completed, and no trials are currently active. The drug is investigational and has not received FDA approval.

What clinical trials is DMT210 5% in?

DMT210 5% has been studied in one completed Phase 2 trial, NCT03003104, titled DMT210 Topical Gel in the Treatment of Acne Rosacea. The trial enrolled 107 participants in the United States, was randomized, double blind, and placebo controlled, and included adults 18 years and older.

Is DMT210 5% the same as DMT210 Topical Gel 5%?

Yes, DMT210 5% and DMT210 Topical Gel 5% refer to the same investigational product from Dermata Therapeutics, Inc. The two names describe the same topical gel formulation being studied for acne rosacea.