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Dermata Receives Notice of Acceptance of Australian Patent Application for Topical Application of Dermal Fillers with its Bioneedle Delivery System

(Positive)
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Dermata (Nasdaq:DRMA) received notice of acceptance from the Australian Patent Office for Australian Patent Application No. 2020315876, covering topical delivery of dermal fillers using its Bioneedle Delivery System (BDS). The patent will be automatically issued three months after acceptance unless a third party files an opposition.

The acceptance would be Dermata's first patent, if issued, for BDS with dermal fillers and adds to existing allowed and issued BDS patents for botulinum toxin in the US, Australia, and Japan. The company noted a strategic shift to selling direct to skincare professionals.

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Positive

  • Australian patent accepted for topical dermal filler use (Application No. 2020315876)
  • Strengthens global IP alongside existing BDS patents for botulinum toxin in US, Australia, Japan
  • Commercial channel shift to direct sales to skincare professionals could improve market access

Negative

  • Issuance subject to opposition: patent auto-issues in three months unless challenged
  • No financial metrics disclosed to quantify potential commercial benefit or timing

News Market Reaction – DRMA

+7.50%
3 alerts
+7.50% Session close to close
+3.9% Peak Tracked
$5.19M Market Cap
0.1x Rel. Volume

In the Apr 2 session, DRMA gained 7.50%, reflecting a notable positive market reaction. Argus tracked a peak move of +3.9% during that session. Our momentum scanner triggered 3 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock moved +7.5% in the session following this news. A strong positive reaction aligns with Der...
Analysis

The stock moved +7.5% in the session following this news. A strong positive reaction aligns with Dermata’s effort to build a defensible IP portfolio, now extending BDS use from botulinum toxin into topical dermal fillers. Prior Australian IP news on Jan 20, 2026 drew a weaker price response, so a larger move would mark a shift in how investors value patent progress. However, the effective $100,000,000 shelf registration preserves capacity for future capital raises, which could influence longer-term trading dynamics.

Key Figures

Australian patent application: 2020315876 Issuance window: 3 months Shelf registration capacity: $100,000,000
3 metrics
Australian patent application 2020315876 Topical dermal filler program using Bioneedle Delivery System
Issuance window 3 months Automatic Australian patent issuance after acceptance absent third-party opposition
Shelf registration capacity $100,000,000 Maximum aggregate offering under S-3 shelf filed Nov 21, 2025

Historical Context

5 past events · Latest: Mar 26 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 26 Earnings and update Positive -13.9% Year-end 2025 results, $7.5M cash, $15.4M raised, DTC pivot to Tome.
Mar 10 Management hire Positive -4.5% Appointment of VP Marketing to lead Tome skincare brand launch.
Mar 05 Brand launch Positive +2.5% Unveiling Tome consumer skincare brand with mid-2026 acne product plan.
Jan 20 Patent grant Positive -5.7% Australian patent grant for Spongilla-based acne treatment technology.
Dec 29 Private placement Neutral +22.6% Up to $12.4M private placement with $4.1M upfront and warrant coverage.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent positive strategic and IP updates have often seen mixed-to-negative next-day moves, while financing and brand-launch news have occasionally drawn stronger positive reactions.

Recent Company History

Over the last several months, Dermata has focused on repositioning toward over-the-counter skincare and strengthening its IP. An Australian acne patent grant on Jan 20, 2026 and today’s Australian patent acceptance both build this estate. Corporate updates on Mar 26, 2026 highlighted cash of $7.5M and a pivot to the Tome brand, following a $4.1M private placement closed on Dec 29, 2025. The new Australian dermal filler patent acceptance extends this IP strategy into aesthetic fillers alongside prior BDS-related patents.

Key Terms

dermal fillers, botulinum toxin, hyperhidrosis
3 terms
dermal fillers medical
"topical dermal filler program utilizing its BDS."
Dermal fillers are injectable products placed under the skin to restore lost volume, smooth wrinkles, or enhance facial contours; think of them as temporary internal padding that plumps and reshapes like adding a cushion under a sagging fabric. They matter to investors because demand, pricing, regulatory approvals, safety records, and product longevity directly affect revenue, margin and legal risk for companies in medical aesthetics and pharmaceutical manufacturing.
botulinum toxin medical
"patents in the US, Australia, and Japan covering their BDS with botulinum toxin for the treatment of hyperhidrosis"
A potent bacterial protein that temporarily blocks nerve signals to muscles, causing controlled muscle relaxation; it is used as a prescription treatment for movement disorders, excessive sweating and other medical conditions, and widely in cosmetic procedures to reduce wrinkles. For investors, botulinum toxin is a high-value pharmaceutical product whose sales depend on regulatory approval, safety profile, manufacturing precision and market demand—think of it as a precision tool whose performance and rules determine its commercial value.
hyperhidrosis medical
"BDS with botulinum toxin for the treatment of hyperhidrosis"
Hyperhidrosis is a medical condition in which a person sweats far more than needed to cool the body, like a thermostat stuck on high. It matters to investors because the condition creates demand for treatments, devices and ongoing services; changes in approvals, patent protection, insurance coverage or new therapy options can affect company sales, recurring revenue and growth prospects in the broader medical and consumer health markets.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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- This would be Dermata's first patent, if issued, covering the use of its Bioneedle Delivery System ("BDS") with dermal fillers -

- The Company also has allowed and issued patents in the US, Australia, and Japan covering their BDS with botulinum toxin for the treatment of hyperhidrosis -

SAN DIEGO, CA / ACCESS Newswire / April 2, 2026 / Dermata Therapeutics, Inc. (Nasdaq:DRMA)(Nasdaq:DRMAW) ("Dermata" or the "Company"), a science-driven leader in dermatologic solutions, today announced the Australian Patent Office has accepted its patent application for its topical dermal filler program utilizing its BDS. The patent, entitled "Compositions for the treatment of conditions by dermal fillers," (Australian Patent Application No. 2020315876) continues to strengthen Dermata's global intellectual property portfolio for its BDS programs. The patent will be automatically issued three months after acceptance unless a third party files an opposition.

"Our receipt of a notice of acceptance for this Australian patent marks a significant milestone in advancing how dermal fillers can be delivered and potentially expands their uses in the aesthetic market," said Gerry Proehl, Chairman, President, and CEO of Dermata. "Instead of traditional injectable applications, we believe topical delivery of dermal fillers opens the door to a wide range of uses, from smoothing fine lines and restoring skin hydration, to enhancing skin barrier function and supporting skin health. With our recent shift to selling direct to skincare professionals, we believe our BDS has the potential to fundamentally transform aesthetic treatments by enabling a non-invasive, topical approach, while expanding access, improving patient comfort, and redefining the aesthetic standard of care. We are excited about the opportunities this innovation creates as we continue to push the boundaries of what's possible in skincare," Mr. Proehl concluded.

About Bioneedle Delivery System

BDS is our topical treatment system that utilizes wild-harvested Spongilla lacustris to aid in the intradermal delivery of macromolecules, such as botulinum toxin or dermal fillers, through topical application by a professional. These macromolecules are highly effective and approved for the treatment of multiple aesthetic skin conditions, but typically must be injected, sometimes requiring numerous injections, which can be painful for consumers. BDS works by creating millions of microchannels in the skin to allow for the topical application of macromolecules allowing for streamlined application and potentially expanded uses.

About Dermata Therapeutics

Dermata Therapeutics is a scientific leader in dermatologic solutions that recently announced a strategic pivot from pharmaceutical development to begin focusing on the development and commercialization of direct-to-consumer skincare solutions. The Company is currently developing two products, a first-of-its-kind skin refresh and an acne treatment, both which incorporate Dermata's Bioneedle. The Company plans to launch its initial product in the middle of 2026 with additional innovations planned to follow. Dermata is headquartered in San Diego, California. For more information, or to join our mailing list, please visit http://www.dermatarx.com/.

Forward-Looking Statements

Statements in this press release that are not strictly historical in nature are forward-looking statements. These statements are based on the Company's current beliefs and expectations and new risks may emerge from time to time. Forward-looking statements are subject to known and unknown risks, uncertainties, assumptions, and other factors including, but are not limited to, statements related to: Dermata's shift to prioritize commercial sale of skincare products; the anticipated benefits of Dermata's strategic shift, including acceleration of its path to commercialization, reduction of regulatory burdens, and expansion into additional markets; the expected timing and success of any planned or future product launches; whether allowed patent applications will proceed to issuance without interruption, if at all, and whether pending or issued patents will provide adequate protection for the Company's product candidates, if approved. These statements are only predictions based on current information and expectations and involve a number of risks and uncertainties. Actual events or results may differ materially from those projected in any of such statements due to various factors, including the risks and uncertainties inherent in product development and commercialization, and the fact that past results may not be indicative of future results. For a discussion of these and other factors, please refer to Dermata's filings with the Securities and Exchange Commission. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. This caution is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All forward-looking statements are qualified in their entirety by this cautionary statement and Dermata undertakes no obligation to revise or update this press release to reflect events or circumstances after the date hereof, except as required by law.

Investors:
Cliff Mastricola
Investor Relations
cmastricola@dermatarx.com

SOURCE: Dermata Therapeutics



View the original press release on ACCESS Newswire

FAQ

What did Dermata (DRMA) announce about the Australian patent on April 2, 2026?

Dermata announced acceptance of its Australian patent application for topical dermal fillers using BDS. According to the company, Australian Patent Application No. 2020315876 was accepted and will automatically issue in three months unless opposed by a third party.

Does the accepted Australian patent mean Dermata's BDS for dermal fillers is fully protected now?

Not yet fully issued; acceptance is a key step toward grant but not final. According to the company, the patent will automatically issue three months after acceptance unless a third party files an opposition, creating potential challenge risk.

How does the Australian acceptance affect Dermata's global intellectual property for BDS (DRMA)?

The acceptance expands Dermata's BDS patent portfolio beyond existing botulinum toxin patents. According to the company, this would be its first patent covering BDS with dermal fillers if it proceeds to grant, strengthening global IP coverage.

What commercial strategy did Dermata (DRMA) highlight alongside the patent news?

Dermata said it is shifting to selling direct to skincare professionals to broaden access. According to the company, the move aims to enable non-invasive, topical aesthetic treatments and improve patient comfort and practitioner access.

What is the timeline and next step after the Australian patent acceptance for Dermata (DRMA)?

The patent acceptance triggers a three-month period before automatic issuance unless opposed. According to the company, if no third party files an opposition within that period, the patent will be issued automatically.