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Title   A Phase III Efficacy and Safety Study of Intravenous Retosiban Versus Placebo for Women in Spontaneous Preterm Labor (NEWBORN-1)
Disease/Condition   Women`s Health

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Eligibility Criteria   Ages Eligible for Study: 12 Years to 45 Years (Child, Adult) Genders Eligible for Study: Female Accepts Healthy Volunteers: No Click here for eligibility requirements
Principal Investigator   Ashlesha Dayal, MD
Contact Name   Melissa Hudson
Phone   (718) 405-8214
Contact Email
Protocol Number   IRB# 15-10-340
Inclusion/Notes   This information was obtained from
Status   Enrolling
Adult Clinical Trial   Yes
Pediatric Clinical Trial   Yes