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Daré Bioscience Initiates Phase 2 Study of DARE-HPV, a Novel Pharmacologic Treatment for Persistent High-Risk HPV Infection with No FDA-Approved Therapies

Each year, an estimated six million women in the United States acquire a high-risk HPV infection — and there are no FDA-approved treatments DARE-HPV development is backed by a $10 million U.S. government (ARPA-H)-funded contract; topline data readout expected in 2027 SAN DIEGO, May 18, 2026 (GLOBE NEWSWIRE) -- Daré Bioscience, Inc. (NASDAQ: DARE), a purpose-driven health biotech company solely focused on closing the gap in women’s health between promising science and real-world solutions, today

articleDare Bioscience, Inc.May 18, 202612/company/dare-bioscience-inc/news/dare-bioscience-initiates-phase-2-study-of-dare-hpv-a-novel-pharmacologic-treatment-for-persistent-high-risk-hpv-infection-with-no-fda-approved-therapies
Daré Bioscience Initiates Phase 2 Study of DARE-HPV, a Novel Pharmacologic Treatment for Persistent High-Risk HPV Infection with No FDA-Approved Therapies

About this update from Dare Bioscience, Inc.

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More updates from Dare Bioscience, Inc.

HPV infectionDARE-HPVcervical cancerpharmacologic treatmentclinical studywomen’s healthclinical developmentcervical diseasePhase 2 study