Precision diagnostics startup launches prenatal screen

UNITY assesses fetal risk for single-gene disorders from single tube of mother’s blood

DDNews Staff
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MENLO PARK, Calif.—BillionToOne, a venture-backed precision diagnostics company, recently announced that its first product, UNITY, is now available for commercial and clinical use.
Powered by BillionToOne’s patent-pending molecular counting technology, UNITY is reportedly the only prenatal screen that tests cell-free fetal DNA for cystic fibrosis, spinal muscular atrophy (SMA) and sickle cell disease using just one tube of blood from the mother. With the completion of analytical and regulatory validation of UNITY, the company will make the test available at select clinics through its Early Access Program, with plans for a broader commercial launch later this year.
“We’re extremely excited about the commercial launch of UNITY, which will make the existing carrier screening process 10 times more accurate and efficient,” said Oguzhan Atay, CEO and co-founder of BillionToOne. “Making UNITY available through our Early Access Program will be the first step in ensuring that all mothers have access to the information they need to help them better prepare for a safe and healthy pregnancy.”
The American College of Obstetricians and Gynecologists (ACOG) recommends that every pregnant woman be screened for her carrier status for cystic fibrosis, SMA, sickle cell disease and thalassemias.
UNITY addresses the many challenges of traditional prenatal screening. It is the first carrier screening with reflex noninvasive prenatal testing for all ACOG-recommended disorders, meaning that once the mother is found to be a carrier, her blood is also analyzed to determine if her baby is at high risk for being affected by the genetic disorder. The entire UNITY screening process takes up to two weeks, compared to 12 weeks or more for traditional carrier screening—saving time and money for parents and reducing workflow for clinicians.   

DDNews Staff

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