A novel intravaginal ring technology featuring the sustained release of natural progesterone for the prevention of preterm birth in at-risk women
Project Number5R44HD101169-03
Contact PI/Project LeaderFRIEND, DAVID R
Awardee OrganizationDARE BIOSCIENCE, INC.
Description
Abstract Text
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.
Public Health Relevance Statement
Infants that are born prematurely, before 37 weeks of pregnancy, are likely to have more health problems than
those carried to term, including serious problems that affect the brain, lungs, vision, and hearing. Progesterone
is a natural hormone that is involved in maintaining healthy pregnancies, and progesterone supplementation is
the gold standard of treatment for women who are at high risk for premature birth. This project aims to develop
an intravaginal ring device to supply bioidentical progesterone to the cervix and vaginal epithelia of at-risk
women, to prevent preterm birth and improve neonatal outcomes.
NIH Spending Category
No NIH Spending Category available.
Project Terms
Advanced DevelopmentAffectAmerican College of Obstetricians and GynecologistsBiological SciencesBrainCenters for Disease Control and Prevention (U.S.)Cervix UteriChildClinic VisitsClinical ResearchCollaborationsCountryDataDevicesDiseaseDoseDrug KineticsEconomic BurdenEnsureEpitheliumFaceFemaleFriendsGelGenesHealthHearingHigh Risk WomanHormonesIn VitroInfant MortalityInfectionInflammationIntramuscular InjectionsLaboratoriesLength of StayLungMaternal-fetal medicineMeasuresMedical Care CostsMethodsNecrotizing EnterocolitisOregonOutcomePatientsPharmaceutical PreparationsPhasePostmenopausePreclinical dataPregnancyPregnancy OutcomePregnant WomenPremature BirthPremature InfantPreventionProductionProgesteronePropertyQuality ControlRecommendationReportingRiskRisk FactorsRisk ReductionSafetyScienceSecond Pregnancy TrimesterSelf AdministrationSocietiesSpecific qualifier valueSupplementationSurvivorsSystemTechnologyTestingUnited StatesUnited States National Institutes of HealthUniversitiesVaginaVaginal GelVaginal RingVisionWomanWorld Health Organizationcapsuleclinical riskcomparativecostfirst-in-humanhealthy pregnancyhigh riskimprovedin vivoliquid chromatography mass spectrometrymanufacturemeetingsneonatal outcomenoveloff-label useopen labelpharmacologicphase III trialpreclinical studyprematurepreventprimary endpointrespiratory distress syndromeskillssocialstability testingwomen's diagnosiswomen's treatment
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
865
DUNS Number
788494669
UEI
UC4EFLZHANH4
007495317
N/A
Project Start Date
12-December-2023
Project End Date
30-November-2025
Budget Start Date
01-December-2024
Budget End Date
30-November-2025
Project Funding Information for 2025
Total Funding
$1,016,258
Direct Costs
$753,962
Indirect Costs
$198,117
Year
Funding IC
FY Total Cost by IC
2025
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$1,016,258
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R44HD101169-03
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5R44HD101169-03
Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5R44HD101169-03
Clinical Studies
No Clinical Studies information available for 5R44HD101169-03
News and More
Related News Releases
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History
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Similar Projects
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