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Dermata Therapeutics Inc - DRMAW STOCK NEWS

Welcome to our dedicated page for Dermata Therapeutics news (Ticker: DRMAW), a resource for investors and traders seeking the latest updates and insights on Dermata Therapeutics stock.

Overview of Dermata Therapeutics Inc

Dermata Therapeutics Inc (NASDAQ: DRMA, DRMAW) is a clinical‐stage, late-stage biotechnology company dedicated to the discovery, development, and commercialization of innovative topical treatments for both medical and aesthetic skin conditions. Utilizing its proprietary Spongilla technology, derived from a naturally sourced freshwater sponge, the Company is committed to addressing significant unmet needs in the dermatological space with cutting-edge solutions that combine mechanical and chemical approaches to treatment.

Innovative Technology and Product Pipeline

The foundation of Dermata’s innovation is its Spongilla technology platform. This proprietary system allows for the formulation of both singular and combination products that target the dermis with unprecedented precision. The Company has developed two primary product candidates:

  • DMT310: A once‐weekly, topical pharmaceutical candidate designed primarily for the treatment of moderate‐to‐severe acne. Through a blend of mechanical exfoliation, collagen stimulation, and chemical actions, DMT310 aims to provide a multi‐mechanism treatment strategy that addresses inflammatory and noninflammatory lesions. In clinical studies, this candidate has been evaluated not only for acne but also for conditions such as rosacea and psoriasis.
  • DMT410: Leveraging the same innovative platform, DMT410 represents a novel approach for the topical intradermal delivery of botulinum toxin. By using the mechanical attributes of Spongilla technology to create microchannels in the skin, DMT410 is positioned as a potential solution for hyperhidrosis as well as multiple aesthetic skin conditions without the need for traditional injections.

Clinical Development and Research

Dermata Therapeutics is well recognized for its rigorous clinical research programs. The Company’s lead candidate, DMT310, is currently being evaluated in a pivotal Phase 3 study, known as the Spongilla Treatment for Acne Research (STAR-1) trial. This randomized, double-blind, placebo-controlled study is designed to assess the efficacy, safety, and tolerability of DMT310 in a broad patient population suffering from moderate-to-severe facial acne. The study incorporates industry-standard assessment tools such as lesion counts and the Investigator Global Assessment (IGA) scale to ensure that the data accurately reflects patient outcomes.

In parallel, DMT410 is advancing as a novel method of delivering botulinum toxin topically. The approach aims to eliminate the discomfort associated with repeated injections and potentially offer a more seamless treatment solution for conditions like hyperhidrosis and other aesthetic challenges. The Company’s exploration into combination regimens and potential partnership opportunities further underscores its commitment to broadening its therapeutic portfolio.

Market Position and Competitive Landscape

As a late-stage biotechnology company headquartered in San Diego, California, Dermata is strategically positioned within the competitive dermatology and aesthetic medicine markets. The Company addresses large segments of the patient population that suffer from acne—affecting millions annually—as well as individuals seeking alternatives to invasive cosmetic treatments. Dermata’s commitment to innovation is highlighted by its robust clinical trial design that focuses on tangible, patient-centric outcomes.

Why Dermata Therapeutics Stands Out

Expertise and Robust Research: The Company's extensive clinical development efforts, meticulous trial designs, and proprietary technology contribute to its high level of expertise and trustworthiness within the biotechnology space.

Innovative Therapeutic Approaches: By combining a naturally sourced technology with advanced pharmaceutical formulation, Dermata Therapeutics is pioneering new methods to target skin conditions at their root. This multifaceted approach not only enhances treatment efficacy but also addresses common limitations of existing therapies.

Broad Clinical Applications: With candidates targeting conditions such as acne, rosacea, psoriasis, and hyperhidrosis, Dermata is preparing to impact several critical areas of dermatology. Each product candidate is developed to be patient-friendly, reflecting the Company’s focus on safety, simplicity, and improved quality of life for sufferers of these conditions.

Operational Excellence and Industry Credibility

Dermata Therapeutics demonstrates strong operational capability rooted in a deep understanding of biological science and dermatology. The Company's research is conducted under rigorous standards and is backed by its strategic location in San Diego—a hub for biotechnology and medical research. This geographical and intellectual positioning further enhances its authoritativeness and trustworthiness in the field.

Conclusion

In summary, Dermata Therapeutics Inc is a highly specialized biotechnology company with a distinct focus on developing once-weekly, topical treatments for challenging dermatological conditions. Through its innovative Spongilla technology and dedicated clinical programs, the Company strives to shift treatment paradigms in both medical and aesthetic dermatology. Investors and industry specialists can appreciate the solid research framework and strategic execution that underpin Dermata’s quest to address pervasive skin conditions with novel, less invasive therapies.

Rhea-AI Summary

Dermata Therapeutics announced the exercise of warrants, resulting in approximately $2.66 million in gross proceeds. The warrants were priced at $5.16 per share, a reduction from their original prices of $9.7665 and $32.40. This transaction involved a total of 516,336 shares of the company's common stock. The closing of this offering is expected around May 21, 2024, pending customary conditions.

In exchange, Dermata will issue new Series A and Series B warrants, exercisable immediately and with different terms. Series A warrants cover 601,174 shares, priced at $4.91 per share, and have a term of five and a half years. Series B warrants cover 431,498 shares, with a two-year term.

The proceeds will fund general corporate purposes including ongoing research, clinical trials, and potential acquisitions. H.C. Wainwright & Co. acted as the exclusive placement agent for this offering.

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Dermata Therapeutics (Nasdaq: DRMA) reported its first quarter 2024 financial results and provided a corporate update. The company is on track with its DMT310 Phase 3 STAR-1 clinical trial for acne, aiming to complete enrollment by end of 2024 with topline data expected in Q1 2025. Dermata is also in discussions for partnerships for its botulinum toxin delivery program, DMT410, and has received a Japanese patent for treating hyperhidrosis. Financially, Dermata ended Q1 2024 with $4.7 million in cash, down from $7.4 million at the end of 2023, following a $3.1 million net loss. Expenses for R&D and G&A increased due to higher clinical trial and stock-based compensation costs.

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Dermata Therapeutics, Inc. (Nasdaq:DRMA) will provide a corporate update and hold a live Q&A session at the Emerging Growth Conference on April 3, 2024. CEO Gerry Proehl will discuss the company's progress and answer audience questions. The event will be held online, allowing shareholders and investors to interact in real-time.
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Dermata Therapeutics, Inc. will be featured at the Emerging Growth Conference on February 7, 2024, providing an overview of the Company's business and allowing for audience interaction. CEO Gerry Proehl will answer questions in real time, offering existing shareholders and the investment community valuable insights.
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Dermata Therapeutics, Inc. (Nasdaq:DRMA, DRMAW) has received its first patent in Japan for DMT410, a program using Spongilla technology to deliver botulinum toxin topically for hyperhidrosis. The Japanese prevalence of hyperhidrosis in 2022 was 10%, with approximately 6% having primary axillary hyperhidrosis. The company is currently discussing partnership opportunities to advance the development of DMT410.
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Tesla Inc. (TSLA) Announces Record-Breaking Q3 Earnings, Surpassing Analyst Expectations
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Dermata Therapeutics, Inc. (NASDAQ:DRMA)(NASDAQ:DRMAW) announces FDA agreement for DMT310 Phase 3 clinical trial protocols, aiming to evaluate the efficacy and safety of once-weekly treatments for moderate-to-severe acne patients. Topline results from STAR-1 clinical trial expected in Q1 2025. DMT310 may be the first once-weekly, topical acne treatment.
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Dermata Therapeutics, Inc. (NASDAQ:DRMA)(NASDAQ:DRMAW) announced a definitive agreement for the immediate exercise of outstanding warrants to purchase up to 3,472,095 shares of common stock at a reduced price of $0.6511 per share. The offering is expected to close soon.
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Dermata Therapeutics, Inc. (NASDAQ:DRMA)(NASDAQ:DRMAW) reported $6.8 million in gross proceeds from financings, FDA feedback on Phase 2 meeting package, and start-up activities for DMT310 Phase 3 STAR-1 clinical trial in acne.
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Dermata Therapeutics to present at H.C. Wainwright 25th Annual Global Investment Conference
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FAQ

What is the current stock price of Dermata Therapeutics (DRMAW)?

The current stock price of Dermata Therapeutics (DRMAW) is $0.0298 as of April 22, 2025.

What is the core focus of Dermata Therapeutics Inc?

Dermata Therapeutics Inc is dedicated to developing once-weekly, topical treatments for medical and aesthetic skin conditions using its proprietary Spongilla technology platform.

What distinguishes DMT310 from other acne treatments?

DMT310 is designed as a once-weekly topical treatment targeting both inflammatory and noninflammatory acne lesions using a unique combination of mechanical exfoliation and chemical activity, potentially addressing limitations of current therapies.

How does the Spongilla technology work?

Spongilla technology utilizes naturally sourced freshwater sponge components to create microchannels in the skin, facilitating the targeted delivery of active compounds and enhancing treatment efficacy.

What therapeutic areas are addressed by Dermata's product candidates?

The Company is focused on treating moderate-to-severe acne, rosacea, psoriasis with DMT310, and using DMT410 for hyperhidrosis and various aesthetic skin conditions through an innovative, needle-free delivery approach.

How are Dermata's clinical trials structured?

Dermata’s clinical trials, such as the Phase 3 STAR-1 study for DMT310, are randomized, double-blind, and placebo-controlled, with endpoints including lesion counts and Investigator Global Assessment scores to rigorously evaluate treatment efficacy and safety.

What is the significance of the Company’s San Diego headquarters?

Headquartered in San Diego, California—a hub for biotech innovation—Dermata benefits from access to cutting-edge research, strategic collaborations, and a robust network of clinical expertise.

How does Dermata plan to differentiate itself in the market?

Through its innovative technology platform, comprehensive clinical programs, and multi-mechanism approach to treatment, Dermata aims to offer therapies that are more effective, patient-friendly, and less invasive compared to traditional options.

What partnerships or collaborations support Dermata’s development efforts?

While the Company maintains a strong internal research framework, it also pursues strategic discussions and collaborative opportunities to enhance its clinical development programs and broaden its therapeutic portfolio.
Dermata Therapeutics Inc

Nasdaq:DRMAW

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2.52M
Biotechnology
Pharmaceutical Preparations
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United States
SAN DIEGO