14-221 - Specimen Collection From Pregnant Women Who are at Increased Risk for Fetal Chromosome DisorderStatus: open
Collection of Whole Blood Specimens from Pregnant Women at Increased Risk for Fetal Chromosomal Abnormality for use in Development of a Noninvasive Prenatal Test in Detection of the Relative Quantity of Chromosomal Material in Circulating Cell-Free DNA Extracted From Maternal Plasma
Treatment for Fetal Aneuploidy / Down Syndrome
If you have questions about this trial or are interested in participating, please contact this Clinical Trial’s Coordinator by email at firstname.lastname@example.org.
The specimen collection is designed for the purpose of the development of a noninvasive prenatal test for T21. IRB Number 14-221
SponsorsThis trial is sponsored by Sequenom, Inc..
Providers Associated With This Trial
- Susan L. Baker, M.D.Maternal-Fetal PhysicianAssociate Professor of Obstetrics and Gynecology