Last updated on April 2018

Patients are needed to participate in a clinical research study to evaluate Premature Birth

Brief description of study

As part of the continuing effort to study the benefit and risks of 17P and preterm delivery, this study is designed as a multi-center, randomized, double-blind, vehicle-controlled clinical trial of 17P for the prevention of preterm birth prior to 35 weeks, 0 days of gestation in women with a singleton pregnancy, aged 18 years or older, with a previous singleton spontaneous preterm delivery. The study also includes a population pharmacokinetic (PK) substudy to assess the hydroxyprogesterone caproate (HPC) exposure-response relationship and the effect of body mass index (BMI) on the PK of 17P.

Clinical Study Identifier: NCT01004029

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Gina Leone

HWC Women's Research Center
Englewood, OH United States

Recruitment Status: Closed

Brief Description Eligibility Contact Research Team

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