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Medical News

Rapid HIV Antibody Test Wins Approval Ahead of Licensing

March 24, 2004

The Food and Drug Administration has given approval for OraSure Technologies Inc. to market its OraQuick Rapid HIV-1/2 Antibody test, which allows simultaneous testing for HIV-1 and HIV-2 in blood specimens. Previously, the test was approved only for the detection of the Type 1 form of HIV. The company said it obtained the approval in anticipation of receiving a worldwide, non-exclusive license to certain HIV-2 patents held by Bio-Rad Laboratories Inc., which it expects in the near future. In addition, OraSure is seeking FDA approval of the OraQuick Rapid HIV-1/2 Antibody Test using oral fluid and plasma samples.

Back to other news for March 24, 2004

Adapted from:
Wall Street Journal
03.24.04

  
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This article was provided by U.S. Centers for Disease Control and Prevention. It is a part of the publication CDC HIV/Hepatitis/STD/TB Prevention News Update.
 

 

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