SBIR/STTR Research Award

A novel intravaginal ring technology featuring the sustained release of natural progesterone for the prevention of preterm birth in at-risk women

Award identifier 6c01896949da1770caebd87d00f91d7f2790078922a7a0b6c5e60b71b2681d3aAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$2,007,831

Program and phase

SBIR · Phase II

Award year

2024

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
DARE BIOSCIENCE, INC.
Proposal award date
2023-12-12
Contract end date
2025-11-30
UEI
UC4EFLZHANH4
Solicitation number
PA19-273
Topic code
NICHD

Research abstract

In the United States, one in ten babies is born prematurely. The earlier in pregnancy a baby is born, the more likely s/he will have an extended hospital stay, as well as serious health complications such as respiratory distress syndrome, necrotizing enterocolitis, vision problems and infection. Women who have had a previous premature birth and women diagnosed with a short cervix in mid pregnancy are at high risk for preterm birth, and are typically prescribed a progesterone product to reduce this risk. There are currently only two general progesterone products available to women at risk for pre-term birth, each having drawbacks associated with variable efficacy and ease of use. Moreover, none of the available progesterone products have received approval from the Federal Drug Administration for use in pregnant women diagnosed with a short cervix. To improve treatment options for women having one or both clinical risk factors for a preterm birth, Daré Bioscience is advancing the development of a novel intravaginal ring, called DARE-FRT1. DARE-FRT1 offers women a patient-friendly, extended-release progesterone product that delivers a relatively constant level of the drug in close proximity to the cervix, where progesterone action regulates inflammation, contractility, and other activities associated with labor. An in vivo preclinical study demonstrated that DARE-FRT1 slowly releases bioidentical progesterone over at least 14 days. Building on these strong foundational studies we aim to (i) complete IND- enabling in vitro DARE-FRT1 product stability studies to ensure consistent and product and (ii) evaluate the comparative pharmacokinetics of different DARE-FRT1 doses in a first-in-human clinical study. Thus, DARE- FRT1 holds promise to be the first simple, safe, and convenient method to extend the term of gestation in women at high risk for preterm birth, improving overall health outcomes, and reducing infant mortality.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

8 SBIR/STTR records share this UEI (2018–2025). Reported award amounts total $6,189,677. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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