Veradermics 2025 Financial Results, IPO & VDPHL01 Updates

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Veradermics Reports Strong 2025 Progress, Successful IPO, and Key VDPHL01 Clinical Milestones

NEW HAVEN, Conn. - Veradermics, Incorporated (NYSE: MANE), a late clinical-stage biopharmaceutical company, announced its financial results for the fourth quarter and full year ended December 31, 2025, alongside significant corporate and clinical advancements. The company emphasized its transformation into a public entity following a successful upsized Initial Public Offering (IPO) in February 2026, which raised approximately $294.8 million in gross proceeds.

Reid Waldman, M.D., CEO of Veradermics, highlighted 2025 as a landmark year, driven by progress in Phase 3 development of VDPHL01, their lead investigational drug for pattern hair loss (PHL). The company anticipates two Phase 3 readouts for male patients in 2026 and aims for a New Drug Application (NDA) submission, while also advancing the first-ever Phase 3 trial of an oral treatment for female PHL. With a robust balance sheet, Veradermics expects its current cash, cash equivalents, and marketable securities to fund operations into 2029, covering multiple anticipated Phase 3 readouts and the potential commercial launch of VDPHL01, if approved.

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About Veradermics, Inc

We are a dermatologist-founded, late clinical-stage biopharmaceutical company focused on developing innovative therapeutics to address pervasive treatment challenges in highly prevalent aesthetic and dermatological conditions. Our initial focus is developing better treatments for pattern hair loss, or PHL, a condition affecting approximately 50 million men and 30 million women in the United States. Current PHL treatment options are limited and therefore are consistently plagued with high rates of treatment failure, patient dissatisfaction and treatment discontinuation. Patients and healthcare providers routinely identify the following shortcomings with currently available treatment options:nSlow onset of hair growth nInconsistent results nInsufficient density of hair growth for patient satisfaction nTolerability issues related to hormonal, mood and cardiac side effects nInconvenient administration nLimited U.S. Food and Drug Administration, or FDA, approved treatment options, and no FDA-approved oral options for women

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