Sangart has announced that an independent data safety monitoring board has recommended the continuation of both Phase III clinical trials of Sangart's lead blood substitute product, Hemospan, under current protocols.
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This recommendation is based on the data safety monitoring board’s (DSMB) review of the blinded data from the first two-thirds of the 830 patients to be enrolled in two ongoing Phase III pivotal studies in Europe.
Robert Winslow, chairman, president and CEO of Sangart, said: “We are pleased to have a second positive DSMB recommendation as we continue to advance these important Phase III studies.”
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