Welcome to our dedicated page for Dermata Therapeutics news (Ticker: DRMA), a resource for investors and traders seeking the latest updates and insights on Dermata Therapeutics stock.
Dermata Therapeutics Inc (DRMA) is a clinical-stage biotechnology company advancing topical treatments for dermatological conditions through its proprietary Spongilla technology. This page aggregates all official press releases, regulatory filings, and news coverage related to the company's clinical programs and corporate developments.
Investors and industry stakeholders will find timely updates on Phase 3 trial progress, FDA communications, and strategic partnerships. Our curated news feed ensures access to verified information about DRMA's innovative approaches to treating acne, rosacea, and other skin conditions.
The archive includes updates across key categories: clinical trial results, intellectual property milestones, product pipeline advancements, and financial disclosures. Each entry provides context about Dermata's unique position in medical dermatology and aesthetic treatments.
Bookmark this page for direct access to DRMA's latest developments. Regular updates offer essential insights for tracking the company's progress in bringing novel topical therapies to market.
Dermata Therapeutics (Nasdaq: DRMA) has announced 50% enrollment in its pivotal Phase 3 STAR-1 clinical trial for DMT310, a novel once-weekly topical treatment for moderate-to-severe acne. The study, which began in December 2023, is the first of two Phase 3 trials aimed at supporting a new drug application (NDA) for DMT310. Topline results are expected in Q1 2025.
The STAR-1 trial is a randomized, double-blind, placebo-controlled study enrolling approximately 550 patients aged 9 and older in the U.S. and Latin America. Primary endpoints include changes in lesion counts and Investigator Global Assessment scores. If approved, DMT310 could become the first once-weekly topical acne treatment, potentially addressing a significant market with about 30 million U.S. acne patients seeking treatment annually.
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.
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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