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Tuesday, February 22, 2022

Allarity Therapeutics Receives Refusal to File Letters from U.S. FDA

 

  • Refusal to File letters concern the new drug application for dovitinib and the DRP®-Dovitinib companion diagnostic pre-market approval application

  • Allarity intends to seek guidance from the FDA on how to further advance dovitinib
    and its accompanying DRP®-Dovitinib companion diagnostic towards approval

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