SBIR/STTR Research Award

Testing a male oral contraceptive targeting Eppin

Award identifier 6264537174f8221b9426c84d981f86503b88f6f2ae892d48427a6cbc3fbb2f64Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,832,621

Program and phase

STTR · Phase II

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
EPPIN PHARMA INC
Proposal award date
2018-06-15
Contract end date
2020-05-31
UEI
VHJQLGNL9T58
Solicitation number
PA16-303
Topic code
NICHD

Research abstract

The global contraceptives market was valued at $billion inand is expected to grow at a CAGR offromtoto reach an estimated value of $billion inThe contraceptive market consists of short term methods such as condoms and oral contraceptionlong term methods including implants and IUDsand permanent methods such as tubal ligations and vasectomiesEppin Pharmaandapos s product has a unique set of characteristicsnamely ease of usehigh efficacyreversibility and no side effectsthat differentiates it favorably from all the other male contraceptive competitorsAn important high impact driver of this market is the prevalence of unintended pregnanciesIn the USthere aremillion unintended pregnancies annually through inconsistent or non use of contraceptionEppin Pharma will be competing in the short term contraception marketThe goal of EPPIN PHARMA INC is to develop a nonhormonal male contraceptive drug that targets the protein EPPINwhich is present on the human sperm surfaceUnlike hormonal contraception which inhibits spermatogenesis our therapeutic agentEPis present in epididymal fluid and binds to EPPIN on the surface of spermThe target EPPIN is only present in the malein testisepididymisand on spermthereby reducing non specific binding concernsThe Specific Aims of this STTR Phaseproposal are designed to build on STTR phasedata and formulate our lead compoundEPas an oral male contraceptive that targets EPPINOur goal in this STTR phase II application is to collect sufficient pharmacology data to conduct a pre IND meeting with the FDASpecific aimwill scale up production of purified EPto support additional preclinical studies and optimize AlphaScreen assays for formulation productsSpecific aimwill complete formulation studies with EPand create a test batch of tablets for preclinical pharmacology studiesSpecific aimwill conduct a monkey contraception fertility study for proof of principleSpecific aimwill conduct oral pharmacokinetics studies in rats and monkeysusing oral gavage in ratsoral dosing of tablets in monkeys and conduct dose range studies for PK PD assessment This research proposal is relevant to public health because it will develop a new male nonhormonal contraceptive that will enhance family planning throughout the world and give men and women additional contraceptive choicesCurrently men are limited in their options for contraception to condoms and vasectomyThereforea non hormonal male contraceptive will fill an unmet need in contraceptionThe proposal is designed to develop a drug for male contraception that targets EPPINThe proposal will provide formulation studiesa monkey contraception study for proof of principle and oral pharmacokinetics studies in rats and monkeys

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

4 SBIR/STTR records share this UEI (2015–2021). Reported award amounts total $3,577,756. Reported amounts are not federal obligations.

Phases: Phase II, Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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