Follow up Study to Assess Long Term Safety and Outcomes in Infants and Children Born to Mothers Participating in Retosiban Treatment Studies

Completed · Phase 3 · Has a placebo group

Conditions studied: Obstetric Labour, Premature

In brief

The primary objective of this study is to assess the safety and outcomes of infants and children who were exposed to retosiban or comparator in utero in the Phase III spontaneous preterm labor (SPTL) treatment studies, to provide assurance that treatment is not associated with significant adverse outcomes in early childhood. The enrolled infants and children will be followed at pre-specified intervals until they reach 24 months chronological age. This study does not require medical interventions or study visits to an investigational site, instead, parents or legal guardians will be prompted at certain time points to complete developmental questionnaires and other data on their children's health status via an electronic device. Data collected during the infant and child follow up study will be managed by a centralized research coordinating center (RCC). Regionally based pediatricians will serve as study principal investigators (referred to as RCC-PIs) for this study. All communications the RCC-PI has with the parent/legal guardian or the child's health care provider (HCP) will occur remotely; there will be no clinic visits.

Key facts

Study ID

NCT02292784

Run by

GlaxoSmithKline

People needed

98

Starts

2015-06-01

Expected to finish

2019-09-02

Last updated by the study team

2020-07-09

Who can join

Age: 0 and older, up to 0. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Mother is randomly assigned and dosed (retosiban or comparator) in 1 of the Phase III SPTL retosiban clinical studies.
• Infant is alive at 28 days post EDD.
• Written informed consent is obtained from the parent(s) or legal guardian(s) of the infant. The parent/legal guardian of subjects aged 12 to 17 years must also provide written agreement for the infant to participate in the study where required by applicable regulatory and country or state requirements.

You may not qualify if…

• There are no formal exclusion criteria for participation.

Where it is running

• GSK Investigational Site — Park Ridge, Illinois, United States
• GSK Investigational Site — Galveston, Texas, United States
• GSK Investigational Site — Ghent, Belgium
• GSK Investigational Site — Freiburg im Breisgau, Baden-Wurttemberg, Germany
• GSK Investigational Site — Jena, Germany
• GSK Investigational Site — Hadera, Israel
• GSK Investigational Site — Haifa, Israel
• GSK Investigational Site — Holon, Israel
• GSK Investigational Site — Kfar Saba, Israel
• GSK Investigational Site — Petah Tikva, Israel
• GSK Investigational Site — Safed, Israel
• GSK Investigational Site — Tel Aviv, Israel
• GSK Investigational Site — Siena, Tuscany, Italy
• GSK Investigational Site — Monza, Italy
• GSK Investigational Site — Miyagi, Japan
• GSK Investigational Site — Miyazaki, Japan
• GSK Investigational Site — Guadalajara, Jalisco, Mexico
• GSK Investigational Site — Monterrey, Nuevo León, Mexico
• GSK Investigational Site — Ciudad Obregón, Sonora, Mexico
• GSK Investigational Site — Seongnam, South Korea
• GSK Investigational Site — Seoul, South Korea
• GSK Investigational Site — Seoul, South Korea
• GSK Investigational Site — Zaragoza, Spain
• GSK Investigational Site — Uppsala, Sweden
• GSK Investigational Site — Sunderland, Tyne & Wear, United Kingdom

Full record on ClinicalTrials.gov

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