SBIR/STTR Research Award

IMMUNODETECTION OF WOMEN AT RISK FOR PRETERM DELIVERY

Award identifier 8f441193092edbcea232f0c112a530424a7439570f620e1ab0bea8994fd46e24Awarding agency Department of Health and Human Services

Award amount

$25,750

Program and phase

SBIR · Phase I

Award year

1992

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Award details

Awarding agency
Department of Health and Human Services
Branch
Not reported
Recipient company
Adeza Biomedical Corpon
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

IT IS THE INTENT OF THE INVESTIGATORS TO DEVELOP A NEW DIAGNOSTIC TEST FOR USE DURING PREGNANCY TO IDENTIFY WOMEN AT ELEVATED RISK FOR PRETERM DELIVERY (PTD). AN IMMUNOASSAY USING A MONOCLONAL ANTIBODY DIRECTED AGAINST ONCOFETAL FIBRONECTION (FFN), A PREGNANCY-RELATED PROTEN OF PLACENTAL ORIGIN FOUND IN THE AMNIOTIC FULID, HAS BEEN STANDARDIEZED FOR THIS PURPOSE. PRELIMINARY STUDIES HAVE SHOWN THAT GREATER THAN 50 NG/ML OF FFN WAS PRESENT IN THE CERVICOVAGINAL SECRETIONS OF 81 PERCENT OF WOMEN AT 23 TO 36 WEEKS OF GESTATION WHO SOUGHT MEDICAL ATTENTION FOR SUSPECTED RUPTURE OF MEMBRANES OF PTD, IN CONTRAST TO ONLY 20 PERCENT (P<0.001) OF 267 WOMEN WITH UNCOMPLICATED TERM PREGNANCIES. THIS DIFFERENE COULD NOT BE EXPLAINED BY DIFFERENCES IN GESTATIONAL AGE AT SAMPLING, CERVICAL DILATION OR PRESENCE OF BLOOD IN THE SECRETIONS. THE PRIMARY OBJECTIVE OF PHASE I WILL BE TO CHARACTERIZE THE RELATIONSHIP BETWEEN CERVICOVAGINAL FFN EXPRESSION AND INCIDENCE OF PTD IN A LONGITUDINAL STUDY OF 100 HIGH RISK PREGNANCIES. IN PHASE I, THE INVESTIGATORS WILL DESIGN A PROSPECTIVE CLINICAL TRIAL TO THOROUGHLY EVALUATE THE DIAGNOSTIC EFFICACY OF AN ANTI-FFN ASSAY FOR COMMERCIAL APPLICATION.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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