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DRMA

Dermata Therapeutics Inc.

Pharmaceutical preparations·Phase 3·San Diego, CA, United States·CEO: Mr. Gerald T. Proehl
Dermatology

DRMA evidence brief

What we can confirm

BioSniper Score:
6.8 / 10
Market Cap:
$5.9M

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

BioSniper Score: 6.8 / 10 · Market Cap: $5.9M
BioSniper AIPage evidence connected

Prepared research question

What matters most for DRMA—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · DRMA

Dermata Therapeutics Inc. (DRMA) is a biopharmaceutical company developing topical treatments for acne and other skin conditions, with its first commercial product launch expected in August 2026.

Key risk: Cash runway limited

6.8/10

BioSniper Score

Based on 2 of 6 signals

Limited data coverage

Market Cap

$5.9M

Cash Runway

—

Lead Asset

—

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 clinical trial for Dermata Therapeutics Inc..

AI OverviewAI overview is shown in English only.

Dermata Therapeutics Inc. (DRMA) is a biopharmaceutical company developing topical treatments for acne and other skin conditions, with its first commercial product launch expected in August 2026.

  • Cash & equivalents of $4.4M as of 2026-06-30 [sec].
  • Net income of -$3.0M as of 2026-06-30 [sec].
  • Shareholders' equity of $3.5M as of 2026-06-30 [sec].
  • First commercial product, Tome™ Foundational Treatment, expected to launch on August 25, 2026 [news · published 2026-08-11].
  • Accumulated deficit of $71.4 million as of September 30, 2025 [sec_mda · as of 2025-11-14].

What works

  • First commercial product launch (Tome™ Foundational Treatment) scheduled for August 25, 2026, indicating progress toward revenue generation [news · published 2026-08-11].
  • Phase 3 study for DMT310 in acne vulgaris has been initiated, showing advancement in clinical development [catalyst].

What to weigh

  • Cash runway is estimated only into the fourth quarter of 2026, suggesting a need for additional capital in the near term [sec_mda · as of 2026-08-11].
  • The company has an accumulated deficit of $71.4 million as of September 30, 2025, and expects to continue incurring net losses [sec_mda · as of 2025-11-14].
  • Future funding requirements are heavily dependent on product revenues from the first launch, which cannot be estimated at this time [sec_mda · as of 2026-08-11].

From the filings

Quoted directly from source documents.

  • Cash runway into Q4 2026

    “We believe that our existing cash and cash equivalents will be sufficient to fund our operating expenses and capital expenditure requirements into the fourth quarter of 2026.”

    SEC MD&A · August 11, 2026

  • First commercial product launch date

    “Dermata announced the launch date of its first commercial product, Tome™ Foundational Treatment, expected on August 25, 2026”

    News · August 11, 2026

  • Accumulated deficit

    “As of September 30, 2025, we had an accumulated deficit of $71.4 million.”

    SEC MD&A · November 14, 2025

  • Phase 3 study start

    “Phase3_Start: A PHASE 3 STUDY OF TOLERABILITY, SAFETY, AND EFFICACY, OF DMT310 IN PATIENTS WITH ACNE VULGARIS”

    Catalysts · December 8, 2023

Catalyst timeline

  • 2023-12-08 · Phase 3 study start for DMT310 in acne vulgaris — Initiation of a Phase 3 tolerability, safety, and efficacy study for DMT310 in patients with acne vulgaris.
Risks & what to watch (3)›

Key risks

  • Cash runway limited — Cash and equivalents of $4.4M as of 2026-06-30 are expected to fund operations only into Q4 2026 [sec_mda · as of 2026-08-11].
  • Accumulated deficit growing — Accumulated deficit reached $71.4M as of September 30, 2025, with continued net losses expected [sec_mda · as of 2025-11-14].
  • Revenue dependence uncertain — Future funding heavily depends on product revenues from first launch, which cannot be estimated [sec_mda · as of 2026-08-11].

What to watch

  • First commercial product launch of Tome™ Foundational Treatment on August 25, 2026 [news · published 2026-08-11].
  • Progress and results of the Phase 3 study for DMT310 in acne vulgaris [catalyst].
  • Ability to raise additional capital given cash runway ending in Q4 2026 [sec_mda · as of 2026-08-11].
  • Financial results and cash position updates in subsequent quarterly reports.

Sources: Catalysts · News · SEC MD&A · Generated October 11, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 2 of 6 signals · derived from public data

Pipeline inputs are unavailable for this score. It uses only the available signals shown below.

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.2

D/E 0.53 · 0% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal4.3

0 buys · 1 sell (180d)

Regulatory

Financials

Short Interest

as of Apr 30, 2026
% of float
6.4%
Days to cover
0.1
Shares short
200,344
Daily short volume (Oct 9, 2026)
21.4%

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

DRMA short interest

Governance

Frequently asked questions

What is the AI investment thesis for Dermata Therapeutics Inc.?

Dermata Therapeutics Inc. (DRMA) is a biopharmaceutical company developing topical treatments for acne and other skin conditions, with its first commercial product launch expected in August 2026.

Who is the CEO of Dermata Therapeutics Inc.?

Mr. Gerald T. Proehl is the chief executive officer of Dermata Therapeutics Inc. (DRMA).

Where is Dermata Therapeutics Inc. headquartered?

Dermata Therapeutics Inc. (DRMA) is headquartered in San Diego, CA, United States.

What therapeutic areas does Dermata Therapeutics Inc. focus on?

Dermata Therapeutics Inc. develops therapies across Dermatology.

923 companies304,844 SEC filings22,644 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.