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Pelthos Therapeutics to Present at 38th Annual ROTH Conference
Globenewswire· 2026-03-12 12:30
Company Overview - Pelthos Therapeutics Inc. is a commercial-stage biopharmaceutical company focused on developing innovative therapeutic products for unmet patient needs [3] - The company's lead product, ZELSUVMI™ (berdazimer) topical gel, 10.3%, is the first and only prescription therapy approved for home use to treat Molluscum contagiosum [3] - Pelthos also offers Xepi® (ozenoxacin) Cream, 1%, for impetigo, and Xeglyze® (abametapir) for head lice [3] Upcoming Events - CEO Scott Plesha will participate in a fireside chat at the 38th Annual ROTH Conference on March 23, 2026, at 3:00 p.m. Pacific Time [1] - A live webcast of the fireside chat will be available on the company's website, with a replay accessible for 90 days post-event [2]
Verrica Pharmaceuticals Reports Fourth Quarter and Full Year 2025 Financial Results
Globenewswire· 2026-03-11 12:00
Core Insights - Verrica Pharmaceuticals reported significant growth in 2025, with total revenue increasing to $35.6 million from $7.6 million in 2024, marking a 368% increase [1][3] - The company achieved a 130% growth in net revenue for its product YCANTH, reaching $15.3 million in 2025, while reducing selling, general, and administrative expenses by over 40% [1][3] - The number of YCANTH dispensed applicator units grew by 99%, totaling 51,296 units in 2025 compared to 25,773 units in 2024 [1][3] Financial Performance - For the fourth quarter of 2025, product revenue was $3.7 million, up from $0.3 million in the same quarter of 2024 [14][17] - The company reported a net loss of $8.1 million for Q4 2025, a significant reduction from a net loss of $16.2 million in Q4 2024 [14][17] - For the full year 2025, the net loss was $17.9 million, compared to a net loss of $76.6 million in 2024, indicating improved financial health [17][19] Product Development and Regulatory Progress - The company is advancing its novel oncolytic peptide VP-315 towards a Phase 3 program for basal cell carcinoma, with supportive data indicating potential abscopal effects [1][5] - The first patient was dosed in a Phase 3 study for YCANTH targeting common warts in December 2025, with plans to initiate a second Phase 3 study in the US and Japan in mid-2026 [1][5] - Verrica gained alignment with the European Medicines Agency, allowing for a streamlined regulatory path for YCANTH's approval in the EU without additional clinical studies [1][4] Market Expansion and Partnerships - The company has launched its first international partnership for YCANTH with Torii Pharmaceutical in Japan, which has already received regulatory approval for the treatment of molluscum contagiosum [4][11] - The company is exploring additional commercialization partnerships to enhance funding and revenue opportunities, particularly following the positive feedback from European regulators [4][5] Operational Efficiency - The company has no outstanding debt and has extended its cash runway into the first quarter of 2027, indicating a strong liquidity position [1][3] - Selling, general, and administrative expenses for the full year 2025 were $35.2 million, down from $58.8 million in 2024, reflecting improved operational efficiency [17][19]
Pelthos Therapeutics to Report Fourth Quarter and Full Year 2025 Financial Results on March 19, 2026
Globenewswire· 2026-03-09 12:30
Company Announcement - Pelthos Therapeutics Inc. will report its fourth quarter and full year 2025 financial results on March 19, 2026 [1] - A conference call will be held at 8:00 a.m. Eastern Time on the same day, followed by a question-and-answer session [1] Conference Call Details - The conference call will be accessible via toll-free number 1-877-451-6152 and international number 1-201-389-0879, with a conference ID of 13758894 [2] - A webcast of the conference call will be available at the provided link [2] Company Overview - Pelthos Therapeutics is a commercial-stage biopharmaceutical company focused on developing products for cutaneous infectious diseases [2] - The lead product, ZELSUVMI™ (berdazimer) topical gel, is the first prescription therapy approved for home use to treat Molluscum contagiosum [2] - The product portfolio also includes Xepi® (ozenoxacin) Cream for impetigo and Xeglyze® (abametapir) for head lice [2]
Pelthos Therapeutics to Present at the Oppenheimer 36th Annual Healthcare Life Sciences Conference
Globenewswire· 2026-02-23 13:00
Core Insights - Pelthos Therapeutics Inc. will have its CEO, Scott Plesha, present at the Oppenheimer 36th Annual Healthcare Life Sciences conference on February 26, 2026 [1] - The company is focused on commercializing innovative therapeutic products for unmet patient needs, particularly in the area of cutaneous infectious diseases [3] Company Overview - Pelthos Therapeutics is a commercial-stage biopharmaceutical company with a portfolio that includes ZELSUVMI™ (berdazimer) topical gel, the first and only prescription therapy approved for home use to treat Molluscum contagiosum [3] - Other products in the company's portfolio include Xepi® (ozenoxacin) Cream for impetigo and Xeglyze® (abametapir) for head lice [3] Investor Engagement - The management team will host one-on-one meetings with investors during the conference, and interested investors can contact their Oppenheimer representative to arrange meetings [2] - A webcast of the presentation will be available on the company's website, with a replay accessible for 90 days following the event [2]
Verrica Pharmaceuticals Appoints Chris Chapman as Chief Commercial Officer
Globenewswire· 2026-02-12 13:00
Core Viewpoint - Verrica Pharmaceuticals Inc. has appointed Chris Chapman as the new Chief Commercial Officer, aiming to enhance the commercialization of its products, particularly YCANTH for molluscum contagiosum and VP-315 for basal cell carcinoma [2][5]. Company Overview - Verrica Pharmaceuticals is focused on developing dermatology therapeutics for skin diseases that require medical interventions [5]. - The company's flagship product, YCANTH (VP-102), is the first FDA-approved treatment for molluscum contagiosum, affecting approximately 6 million people in the U.S., primarily children [4][5]. - YCANTH is also being developed for the treatment of common warts, addressing a significant unmet need in medical dermatology [5]. Leadership Appointment - Chris Chapman brings over 25 years of commercial experience in the pharmaceutical industry, having previously served as Chief Commercial Officer at Dermavant Sciences [2][3]. - His experience includes launching VTAMA for adult plaque psoriasis and leading the U.S. Prescription Business for Galderma [3]. Product Details - YCANTH is a proprietary drug-device combination that allows for precise topical dosing and is administered by healthcare professionals [4]. - The product has shown positive results in two Phase 3 clinical trials involving approximately 500 patients, demonstrating safety and efficacy [4]. - Approximately 250 million lives are eligible for YCANTH coverage by insurance, with commercially insured patients paying $25 per treatment visit [4]. Pipeline Development - Verrica has entered a worldwide license agreement with Lytix Biopharma AS to develop and commercialize VP-315, targeting non-melanoma skin cancers, including basal cell carcinoma and squamous cell carcinoma [5].
Biofrontera Inc. announces sale of license to Xepi® Antibiotic Cream to Pelthos Therapeutics Inc. for up to $10M
Globenewswire· 2025-11-07 13:00
Core Viewpoint - Biofrontera Inc. has divested its US license for Xepi (ozenoxacin) Cream, 1% to Pelthos Therapeutics Inc., receiving a total of up to $10 million, which is expected to strengthen its balance sheet and support its path to profitability [1][2][5]. Financial Summary - The divestiture includes an initial payment of $3 million at closing, an additional $1 million upon availability of the commercial product, and up to $6 million in milestone payments tied to achieving $10 million and $15 million in annual net revenues for Xepi [1][5]. - The transaction is anticipated to bolster Biofrontera's cash position, aiding in funding its operations towards profitability [5]. Business Focus - Biofrontera specializes in photodynamic therapy (PDT) and is focused on expanding the indications for its product Ameluz® for the treatment of actinic keratosis (AK) and potentially other conditions [2][3]. - The company is also involved in clinical trials to extend the use of its products for treating non-melanoma skin cancers and moderate to severe acne [3]. Product Information - Xepi (ozenoxacin) Cream, 1% is a topical non-fluorinated quinolone that is FDA-approved for treating impetigo, a common skin infection caused by Staphylococcus aureus or Streptococcus pyogenes, with no known antibiotic resistance [2].
Pelthos Therapeutics Acquires Xepi® (ozenoxacin) Cream, 1% and Announces $18 Million Private Convertible Notes Financing
Globenewswire· 2025-11-07 13:00
Core Viewpoint - Pelthos Therapeutics has acquired U.S. commercialization rights to Xepi® (ozenoxacin) Cream, a topical treatment for impetigo, marking a significant step in addressing unmet patient needs in pediatric dermatology [1][4][8] Acquisition Details - Pelthos will pay a total of $4.2 million upfront for the acquisition, consisting of $3.0 million to Biofrontera and $1.2 million to Ferrer, with additional payments tied to commercial availability and sales milestones [3][4] - The acquisition is expected to enhance Pelthos's portfolio, which is anchored by its existing product ZELSUVMI™ [8][10] Market Context - Impetigo affects approximately 3 million people annually in the U.S., predominantly children aged 2 to 5, highlighting a significant market opportunity for Xepi [5][8] - The rise of bacterial resistance to common topical antibiotics has created a pressing need for effective alternatives, positioning Xepi as a critical treatment option [6][8] Financing Details - Pelthos has secured $18 million through private convertible notes financing, which will support the acquisition and re-launch of Xepi, as well as the commercialization of ZELSUVMI [2][7][9] - The notes will bear an interest rate of 8.5% per annum and are convertible at an initial price of $34.442 [7][10] Strategic Implications - The acquisition and financing are seen as strategic moves to bolster Pelthos's commercial growth and leverage its existing infrastructure to promote multiple innovative brands [4][10] - The company plans to re-launch Xepi in late 2026, aiming to provide a novel treatment option in the pediatric dermatology space [4][8]
Pelthos Therapeutics Acquires Xepi® (ozenoxacin) Cream, 1% and Announces $18 Million Private Convertible Notes Financing
Globenewswire· 2025-11-07 13:00
Core Viewpoint - Pelthos Therapeutics has acquired U.S. commercialization rights to Xepi® (ozenoxacin) Cream, a topical treatment for impetigo, marking a significant step in addressing unmet patient needs in pediatric dermatology [1][4][8] Acquisition Details - Pelthos will pay a total of $4.2 million upfront for the acquisition, consisting of $3.0 million to Biofrontera and $1.2 million to Ferrer, with additional payments tied to commercial availability and sales milestones [3] - The acquisition is expected to enhance Pelthos's portfolio, which is anchored by its existing product ZELSUVMI™ [8] Market Context - Impetigo affects approximately 3 million people annually in the U.S., predominantly children aged 2 to 5, highlighting a significant market opportunity for Xepi [5][8] - The need for effective alternatives to traditional treatments is underscored by rising bacterial resistance, particularly to commonly used topical antibiotics [6] Financing Details - Pelthos has secured $18 million through private convertible notes financing, which will support the acquisition and re-launch of Xepi, as well as the commercialization of ZELSUVMI [2][7][10] - The notes will bear an interest rate of 8.5% per annum and are convertible at an initial price of $34.442 [7] Strategic Implications - The acquisition of Xepi is seen as a strategic move to leverage Pelthos's existing commercial infrastructure and expand its product offerings in the pediatric and dermatology markets [4][10] - The company aims to re-launch Xepi in late 2026, positioning it as a critical treatment option amid growing concerns over antibiotic resistance [4][8]