Welcome to our dedicated page for Dare Bioscience news (Ticker: DARE), a resource for investors and traders seeking the latest updates and insights on Dare Bioscience stock.
Dare Bioscience Inc (NASDAQ: DARE) is a clinical-stage biopharmaceutical leader advancing innovative therapies for women’s reproductive and sexual health. This dedicated news hub provides investors and healthcare professionals with essential updates on clinical trial progress, regulatory milestones, and strategic partnerships.
Track the latest developments across DARE’s pipeline of non-hormonal contraceptives, sexual health treatments, and cervical health solutions. Our curated news collection includes updates on FDA submissions, trial results for candidates like Ovaprene® and Sildenafil Cream 3.6%, and collaborations advancing women’s healthcare innovation.
Key focus areas include progress toward addressing unmet needs in bacterial vaginosis treatment, female sexual arousal disorder (FSAD), and HPV-related cervical conditions. Bookmark this page for real-time access to earnings announcements, research publications, and licensing agreements that shape DARE’s position in the biopharma sector.
Daré Bioscience (NASDAQ: DARE) has received a $6 million non-dilutive grant installment for developing DARE-LARC1, bringing the total received to $37.8 million of a $49 million commitment. DARE-LARC1 is a preclinical-stage long-acting reversible contraceptive utilizing their intelligent drug delivery system (DARE-IDDS) platform.
The DARE-IDDS platform, originally developed at MIT, features wireless control, precision dosing, and extended duration capabilities. The technology can deliver hundreds of individualized doses over months or years without recharging. Beyond contraception, the platform shows potential applications in obesity, diabetes, and other chronic conditions requiring precise, long-term dosing.
The company is actively exploring strategic partnerships to expand the platform's use beyond reproductive health, with $11.2 million in additional non-dilutive funding available upon achieving specific milestones.
Daré Bioscience (NASDAQ: DARE), a biopharmaceutical company focused on women's health, has scheduled its Q1 2025 financial results and company update conference call for May 13, 2025, at 4:30 p.m. Eastern Time. Investors can access the call via phone at (646) 307-1963 (U.S.) or (800) 715-9871 (toll-free) using conference ID 3461324. A live webcast will be available on the company's investor relations website, with replay access until May 27, 2025.
Daré Bioscience (NASDAQ: DARE) announced that CEO Sabrina Martucci Johnson will deliver a keynote address at the Fierce Pharma Engage summit on April 29, 2025. The presentation, titled 'Breaking Barriers, Building Access: Communicating Bold Moves in Women's Health Innovation,' will focus on the company's expanded business strategy incorporating 503B compounding.
The company recently unveiled a dual-path approach for its proprietary Sildenafil Cream formulation, targeting prescription availability in Q4 2025. Daré's portfolio includes XACIATO™, an FDA-approved bacterial vaginosis treatment licensed to Organon, and several first-in-category candidates:
- Ovaprene® - hormone-free monthly contraceptive (licensed to Bayer)
- Sildenafil Cream, 3.6% - for female sexual arousal disorder
- DARE-HRT1 - bio-identical hormone therapy ring
Daré Bioscience (NASDAQ: DARE) has announced its expanded business strategy featuring a dual-path approach for its proprietary Sildenafil Cream formulation, with plans to make it available via prescription in Q4 2025. The company's President and CEO, Sabrina Martucci Johnson, will present these developments at the Jones Healthcare and Technology Innovation Conference on April 9th, 2025.
The strategy includes utilizing Section 503B compounding to expedite market access for select Daré proprietary formulations. The company is also exploring bringing consumer health products to market without prescription requirements. Additional strategic partnerships and timing updates are expected this quarter.
The presentation will be accessible via webcast at 1:00 p.m. PT, with a replay available until April 23, 2025, through the company's investor relations website.
Daré Bioscience (NASDAQ: DARE) reported its full year 2024 financial results and announced plans to make its proprietary Sildenafil Cream available via prescription through 503B compounding in Q4 2025, expecting to generate revenue and cash flow. The company ended 2024 with $15.7 million in cash and a working capital deficit of $3.2 million.
Financial highlights show reduced expenses, with G&A costs down 24% to $9.2 million and R&D expenses decreased 34% to $14.2 million compared to the previous year. Key pipeline developments include the ongoing Ovaprene® Phase 3 contraceptive study, with approximately 125 women expected to complete six months of use by Q2 2025, supported by a $10.7 million non-dilutive grant.
The company is pursuing a dual-path approach for select proprietary formulations, including both FDA approval and 503B framework distribution. Daré plans to invest less than $1 million to support the Sildenafil Cream 503B initiative and expects to provide strategic partnership updates in Q2 2025.
Daré Bioscience (NASDAQ: DARE), a women's health innovation company, has scheduled its full year 2024 financial results conference call and webcast for March 31, 2025, at 4:30 p.m. Eastern Time. The presentation will include both financial performance review and company updates.
Participants can join via phone at (646) 307-1963 (U.S.) or (800) 715-9871 (toll-free) using conference ID 9767621. A live webcast will be available through the Investors section of Daré's website. The webcast recording will remain accessible for replay until April 14, 2025.
Daré Bioscience (NASDAQ: DARE) and Theramex have entered into a co-development and licensing agreement for Casea S, a potential first-in-category biodegradable contraceptive implant. The product is designed to release contraceptive medication over 18-24 months before dissolving, eliminating the need for surgical removal.
A fully-funded Phase 1 trial is currently ongoing, conducted by FHI 360, investigating pharmacokinetics, removability, safety, and tolerability. Daré has received a royalty-free, exclusive license to the US patents for Casea S. There are currently no development costs for either company due to foundation grant funding.
If Phase 1 results are positive, Daré will be responsible for conducting the Phase II study in the US. Future Phase II and III study funding will be shared between both companies, with terms to be determined based on market opportunity in their respective regions.