FDA recently granted approval of a biological license application from Roche Molecular Systems, Pleasanton, Calif, for the company’s Cobas Zika test, a qualitative nucleic acid test for the detection of Zika virus RNA in individual plasma specimens obtained from volunteer donors of whole blood and blood components, and from living organ donors. The test is intended for use by blood collection establishments to detect Zika virus in blood donations, not for the individual diagnosis of Zika virus infection.
“Today’s action represents the first approval of a Zika virus detection test for use with screening the nation’s blood supply,” said Peter Marks, MD, PhD, director of FDA’s Center for Biologics Evaluation and Research. “Screening blood donations for the Zika virus is critical to preventing infected donations from entering the US blood supply. Today’s approval is the result of a commitment by the manufacturer to work rapidly and collaboratively with FDA and the blood collection industry to respond to a public health crisis and ensure the safety of blood in the United States and its territories.”
In August 2016, FDA issued a final guidance document recommending that all states and territories screen individual units of whole blood and blood components with a blood screening test available under an investigational new drug (IND) application or, when available, with a licensed (approved) test.
Several blood collection establishments previously used the Cobas Zika test under IND authorization in order to follow the recommendations in FDA’s 2016 guidance document. The data collected from that testing, and from additional studies performed by the manufacturer, demonstrated that the Cobas Zika test is an effective test to screen blood donors for Zika virus infection. The test’s clinical specificity was evaluated by testing individual samples from blood donations at five external laboratory sites, resulting in clinical specificity of more than 99%.
The Zika virus is transmitted primarily by Aedes aegypti mosquitos, but it can also be spread through blood transfusion and sexual contact. Although most people infected with Zika virus do not develop symptoms, when symptoms do occur they may include arthralgia (joint pain), conjunctivitis (red, irritated eyes), fever, or maculopapular rash (red area with small bumps). In addition, Zika virus infection can cause a serious neurological disease in adults, and infection during pregnancy can cause serious birth defects.
The Cobas Zika test is intended for use on the fully automated Cobas 6800 and Cobas 8800 systems. The Cobas Zika test, Cobas 6800, and Cobas 8800 systems are manufactured by Roche Molecular Systems Inc.
For more information, visit Roche Molecular Diagnostics.