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Repatha was well tolerated in the extension studies with no new safety signals. The rates of overall adverse events were similar for the two groups, occurring in 80% of patients receiving Repatha and 67% of patients receiving SoC. 2:45 am Roche Hldg's Zika PCR test receives Emergency Use Authorization from the FDA ( RHHBY ) : Co announced that theFDA has issued an Emergency Use Authorization for the LightMix Zika rRT-PCR Test. The product is for use in patients meeting CDC Zika virus clinical criteria and/or CDC Zika virus epidemiological criteria. The test is used for the detection of Zika virus in EDTA plasma or serum samples using Roche's LightCycler 480 Instrument II or cobas z 480 Analyzer. In addition to the LightMix Zika rRT-PCR Test, Roche has also developed the cobas Zika Test for use with the cobas 6800/8800 Systems. This test is available under an Investigational New Drug Application protocol to initiate collection and testing of blood samples for screening. It is currently being utilized in blood centres in the United States. 2:35 am On The Wires (:WIRES) : Royal Philips (PHG) announced the launch of IntelliSpace Cardiovascular 2.1, the latest version of its next-generation Cardiovascular Image and Information Management System. Showcased at the Philips Booth during the ESC Congress 2016, IntelliSpace Cardiovascular provides clinicians with a single point of access anytime and virtually anywhere and allows for web-based echo reporting, delivering diagnostic quality viewing of echo images. Axiall Corporation (AXLL) statement: At approximately 8:40 a.m.
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