STOCK TITAN

Daré Bioscience Announces New NIH Funding Award for Approximately $908,000 to Advance DARE-PTB2 for the Prevention of Preterm Birth

(Moderate)
(Neutral)
Tags

Daré Bioscience (NASDAQ: DARE) announced a new NIH funding award of approximately $908,000 from the Eunice Kennedy Shriver National Institute of Child Health and Human Development to support year-long preclinical development of DARE-PTB2, an early-stage investigational program for preventing idiopathic preterm birth.

The notice of award also includes recommended future-year support of about $1.3 million for initial pharmacokinetic, safety, and toxicity studies. This non-dilutive grant builds on an earlier $400,000 NICHD award in July 2023 that funded proof-of-concept target validation studies with the University of South Florida.

Loading...
Loading translation...

Positive

  • New NIH NICHD grant of approximately $908,000 to advance DARE-PTB2 preclinical development
  • Recommended future-year NIH support of about $1.3 million for PK, safety, and toxicity studies
  • Funding is explicitly described as non-dilutive, supporting advancement without issuing new equity
  • DARE-PTB2 targets a condition with no FDA-approved therapies, addressing a significant unmet need

Negative

  • None.

Market Context

The platform classifies DARE’s short positioning as low. Against that context, the NIH award’s non-d...
Analysis

The platform classifies DARE’s short positioning as low. Against that context, the NIH award’s non-dilutive funding is the main financing support, while the program’s early-stage preclinical status remains the central development risk.

Key Figures

NIH award: $908,000 Future-year support: $1.3 million Prior NICHD award: $400,000 +1 more
4 metrics
NIH award $908,000 New award for DARE-PTB2 preclinical development
Future-year support $1.3 million Recommended support for initial preclinical studies
Prior NICHD award $400,000 July 2023 preclinical development award
Preterm birth definition 37 weeks Birth before 37 completed weeks of pregnancy

Historical Context

5 past events · Latest: Aug 27 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 27 Investor presentation Neutral -2.5% CEO presentation highlighted commercialization efforts, pipeline progress, and potential catalysts over the next 12–18 months.
Aug 26 Phase 1 data publication Positive -8.5% Phase 1 sildenafil cream publication reported tolerability and limited systemic exposure.
Aug 25 CEO investor segment Positive +2.4% CEO segment discussed commercial transformation, product launches, and pipeline advancement including Phase 3 results.
Aug 18 Leadership recognition Positive -5.8% CEO recognition accompanied disclosures on portfolio expansion and commercial product initiatives.
Aug 14 Registered direct offering Negative -34.3% Registered direct offering and warrants targeted $6.0 million in gross proceeds.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent DARE history included positive announcements followed by negative 24-hour reactions of -8.54% and -5.83%, alongside an offering followed by -34.31%.

Key Terms

pharmacokinetic, non-dilutive funding, proof-of-concept, idiopathic preterm birth, +1 more
5 terms
pharmacokinetic medical
"completion of initial preclinical pharmacokinetic, safety, and toxicity studies"
Pharmacokinetic describes how a drug moves through and leaves the body — how it is absorbed, spread to tissues, broken down and excreted — like tracking a package from pickup to delivery and disposal. For investors, these properties determine effective dose, safety risks, how often a medicine must be taken, and how reliably it works, which in turn influence clinical trial success, regulatory approval chances, production complexity and a drug’s commercial value.
non-dilutive funding financial
"This new award provides important non-dilutive funding"
Non-dilutive funding is money a company raises that does not require issuing new shares or reducing existing owners’ percentage ownership, such as grants, certain loans, contract revenue, or licensing deals. It matters to investors because it lets a company finance growth or research without shrinking shareholder stakes or changing control, much like topping up a car’s gas tank instead of selling part of the car to pay for the trip.
proof-of-concept technical
"The funding supported proof-of-concept target validation studies"
A proof-of-concept is a demonstration that shows a new idea or method can work as intended, serving as a small-scale test before full development. For investors, it signals that a concept has been successfully tested in principle, reducing uncertainty about whether it can be practically implemented. This helps determine if further investment or effort is justified to develop the idea further.
idiopathic preterm birth medical
"prevention of idiopathic preterm birth"
A spontaneous birth that occurs before 37 weeks of pregnancy with no identifiable cause after standard medical evaluation. It matters to investors because it defines a patient group for clinical trials and drug development, shapes the size and urgency of markets for preventive or treatment products, and affects regulatory and reimbursement considerations—think of it as a fleet of boats leaving port early without an obvious common engine failure, prompting targeted research and products.
fda-approved regulatory
"there are no FDA-approved therapeutic options available"
FDA-approved means a medical product, drug, device or treatment has passed the U.S. Food and Drug Administration’s review for safety and effectiveness for a specific use. Think of it like a formal safety and performance seal that allows the product to be marketed for that purpose in the U.S.; for investors, approval reduces regulatory uncertainty, enables sales and reimbursement pathways, and can materially affect a company’s revenue prospects and valuation.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

New NIH award will provide approximately $908,000 in year-long support of preclinical development, with potential for an additional future-year grant of approximately $1.3 million

DARE-PTB2 is an early-stage, investigational program focused on developing a potential new therapeutic approach for the prevention of preterm birth

SAN DIEGO, Aug. 31, 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 announced that it received a new notice of award from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) of the National Institutes of Health (NIH) in the amount of approximately $908,000 to advance the Company’s DARE-PTB2 program for the prevention of preterm birth. The notice of award also includes recommended future-year support of approximately $1.3 million for completion of initial preclinical pharmacokinetic, safety, and toxicity studies.

DARE-PTB2 is an early-stage investigational program focused on developing a potential new therapeutic approach for the prevention of idiopathic preterm birth. The program aims to address a significant unmet medical need, as preterm birth remains a leading cause of infant morbidity and mortality worldwide and there are no FDA-approved therapeutic options available to reduce the risk of preterm birth.

“We are grateful for the continued support from the NIH and NICHD for the DARE-PTB2 program and for their recognition of the importance of developing new approaches to address preterm birth. This new award provides important non-dilutive funding to support the continued advancement of DARE-PTB2 and reflects our strategy of leveraging non-dilutive funding opportunities to advance innovative programs addressing significant unmet needs in women’s health,” said Sabrina Martucci Johnson, President and CEO of Daré Bioscience.

The DARE-PTB2 program builds on research previously supported by NICHD. In July 2023, Daré received a notice of award from NICHD of approximately $400,000 to support preclinical development of a potential new therapeutic for the prevention of idiopathic preterm birth. The funding supported proof-of-concept target validation studies conducted in collaboration with the University of South Florida.

“Continued support from the NIH enables us to advance the scientific foundation of the DARE-PTB2 program and further evaluate a potential new therapeutic approach to addressing preterm birth,” said David Friend, PhD, Chief Scientific Officer of Daré Bioscience. “We appreciate the NICHD’s continued commitment to this important area of research and to the development of innovative solutions for women and their babies.”

About DARE-PTB2

DARE-PTB2 is an early-stage, investigational program for the development of a therapeutic treatment to prevent idiopathic preterm birth. The program is focused on a novel therapeutic approach intended to address biological mechanisms associated with preterm birth.

Preterm birth, defined as birth before 37 weeks of pregnancy have been completed, is a significant global health challenge and is associated with substantial morbidity and mortality among infants. Preterm birth can result from a range of underlying causes, and there remains a significant need for therapeutic approaches to reduce the risk of preterm delivery.

About the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NICHD conducts and supports research in the United States and throughout the world on fetal, infant and child development; maternal, child and family health; reproductive biology and population issues; and medical rehabilitation. For more information, visit www.nichd.nih.gov.

The research described in this press release was supported by the NICHD of the NIH under Award Number R41HD113465, or will be supported by the NICHD of the NIH under Award Number R44HD113465. The content of this press release is solely the responsibility of Daré Bioscience and does not necessarily represent the official views of the NIH.

ABOUT DARÉ BIOSCIENCE, INC.

Daré Bioscience (NASDAQ: DARE) is a purpose-driven health biotech company solely focused on closing the gap in women’s health between promising science and real-world solutions. Every innovation Daré Bioscience advances is based in advanced science and backed by rigorous, peer-reviewed research. From contraception to menopause, sexual health to fertility, vaginal health to infectious disease, Daré Bioscience is working to close critical gaps in care using science that serves her needs. For decades, women have been told to “wait it out” or “live with it,” while innovations that could improve their quality of life languish in the regulatory or funding pipeline. With growing awareness around menopause, sexual health, and vaginal health, the conversation is shifting. However, access to proven solutions is lagging. Daré Bioscience is working to change that. Learn more at darebioscience.com.

FORWARD-LOOKING STATEMENTS

Daré Bioscience cautions you that all statements, other than statements of historical facts, contained in this press release, are forward-looking statements. Forward-looking statements, in some cases, can be identified by terms such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “design,” “intend,” “expect,” “could,” “plan,” “potential,” “prepare,” “aim,” “should,” “would,” “build” or the negative version of these words and similar expressions.

In this press release, forward-looking statements include, but are not limited to, statements relating to: receipt of payments under the new NIH award; the potential for an additional future-year NIH grant in support of DARE-PTB2; the extent of preclinical development work that may be completed with the support of NIH funding; plans and timing for continued development of DARE-PTB2; the potential safety and therapeutic benefits of a novel approach for the prevention of preterm birth; Daré’s ability to obtain and leverage non-dilutive funding to advance development of therapeutic candidates for women’s health; and the potential market opportunity for DARE-PTB2.

Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause Daré Bioscience’s actual results, performance or achievements to be materially different from future results, performance or achievements expressed or implied by the forward-looking statements in this press release, including, without limitation, risks and uncertainties related to: Daré Bioscience’s ability to demonstrate satisfactory progress with the DARE-PTB2 project to NICHD and continued compliance with the terms and conditions of the funding award; federal government actions to freeze or terminate NIH grants or significantly reduce the NIH’s budget and research funding; disruptions at the NIH or NICHD due to federal government shutdowns, other funding shortages, policy changes, leadership changes, or significant layoffs or personnel turnover; Daré Bioscience’s ability to raise additional capital when and as needed to execute its business strategy and continue as a going concern; potential suspension and delisting of Daré Bioscience’s common stock from the Nasdaq Capital Market; Daré Bioscience’s dependence on grants and other financial awards from governmental entities and a private foundation; Daré Bioscience’s reliance on third parties to manufacture and conduct preclinical and clinical studies of its product candidates and the risk that those third parties do not perform as expected; failure or delay in starting, conducting and completing preclinical and clinical studies and the inherent uncertainty of outcomes of such development work; Daré Bioscience’s ability to develop, obtain FDA or foreign regulatory approval for, and commercialize its product candidates and to do so on communicated timelines; the risks that positive findings in early clinical and/or nonclinical studies of a product candidate may not be predictive of success in subsequent clinical and/or nonclinical studies of that candidate; the risk that the FDA, other regulatory authorities, members of the scientific or medical communities or investors may not accept or agree with Daré Bioscience’s interpretation of or conclusions regarding data from nonclinical and/or clinical studies of its product candidates; the risk that development of a product candidate requires more clinical or nonclinical studies than Daré Bioscience anticipates, or that the duration of a study or number of study subjects must be significantly greater than anticipated; the loss of, or inability to attract, key personnel; Daré Bioscience’s ability to retain its licensed rights to develop and commercialize a product or product candidate; Daré Bioscience’s ability to satisfy the monetary obligations and other requirements in connection with its exclusive, in-license agreements covering the critical patents and related intellectual property related to its product and product candidates; Daré Bioscience’s ability to adequately protect or enforce its, or its licensor’s, intellectual property rights; disputes or other developments concerning Daré Bioscience’s intellectual property rights; the lack of patent protection for the active ingredients in certain of Daré Bioscience’s product candidates which could expose its products to competition from other formulations using the same active ingredients; product liability claims; governmental investigations or actions relating to Daré Bioscience’s products or product candidates or the business activities of Daré Bioscience, its commercial collaborators or other third parties on which Daré Bioscience relies; changes in healthcare, pharmaceutical, consumer protection or privacy laws and regulatory policies; increased scrutiny from regulators; global trends toward health care cost containment; the effects of macroeconomic conditions, geopolitical events, and major changes and disruptions in U.S. government policies and operations on Daré Bioscience’s ability to raise additional capital or on Daré Bioscience’s operations, financial results and condition, and ability to achieve current plans and objectives; and cybersecurity incidents or similar events that compromise Daré Bioscience’s technology systems and/or significantly disrupt Daré Bioscience’s business or those of third parties on which it relies.

Daré Bioscience’s forward-looking statements are based upon its current expectations and involve assumptions that may never materialize or may prove to be incorrect. All forward-looking statements are expressly qualified in their entirety by these cautionary statements. For a detailed description of Daré Bioscience’s risks and uncertainties, you are encouraged to review its documents filed with the U.S. Securities and Exchange Commission (SEC), including Daré Bioscience’s recent filings on Form 8-K, Form 10-K and Form 10-Q. You are cautioned not to place undue reliance on forward-looking statements, which speak only as of the date on which they were made. Daré Bioscience undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.

Contact:
Daré Bioscience Investor Relations
innovations@darebioscience.com 
Source: Daré Bioscience, Inc.


FAQ

What NIH funding did Daré Bioscience (NASDAQ: DARE) receive for DARE-PTB2 in August 2026?

Daré Bioscience received an NIH NICHD award of approximately $908,000 for DARE-PTB2 preclinical development. According to Daré Bioscience, the year-long funding will support pharmacokinetic, safety, and toxicity work aimed at a novel approach to preventing idiopathic preterm birth.

Is there additional potential NIH funding for Daré Bioscience’s DARE-PTB2 program (DARE)?

Yes. The notice of award includes recommended future-year support of about $1.3 million. According to Daré Bioscience, this prospective funding would help complete initial preclinical pharmacokinetic, safety, and toxicity studies for the DARE-PTB2 preterm birth prevention program.

What is DARE-PTB2 and what condition is Daré Bioscience targeting with DARE?

DARE-PTB2 is an early-stage investigational program to develop a therapeutic to prevent idiopathic preterm birth. According to Daré Bioscience, it uses a novel approach aimed at biological mechanisms linked to preterm birth, addressing a major unmet need in women’s and infant health.

How does the new NIH grant impact Daré Bioscience’s funding strategy for DARE-PTB2 (NASDAQ: DARE)?

The award provides non-dilutive funding, meaning no new shares are issued. According to Daré Bioscience, this supports its strategy of leveraging grants to advance women’s health programs like DARE-PTB2 while limiting shareholder dilution and extending development runway.

What prior NICHD support has Daré Bioscience received for DARE-PTB2 (DARE)?

In July 2023, Daré Bioscience received an NICHD award of about $400,000. According to Daré Bioscience, that earlier funding supported proof-of-concept target validation studies for DARE-PTB2, conducted in collaboration with the University of South Florida.

Why is the DARE-PTB2 preterm birth program significant for Daré Bioscience shareholders (DARE)?

DARE-PTB2 targets idiopathic preterm birth, for which there are no FDA-approved therapies. According to Daré Bioscience, successful development could address a leading cause of infant morbidity and mortality, potentially expanding the company’s women’s health portfolio.