Vifor Pharma Group and Angion Biomedica Corp.’s partnership for ANG-3777 has faced a major setback as the drug candidate missed the primary endpoint in a Phase III trial for its lead indication in kidney transplant patients at risk for developing delayed graft function (DGF), topline data show.
ANG-3777 is in a Phase II trial for another indication, cardiac-surgery associated acute kidney injury (CSA-AKI), but analyst expectations have cooled following the DGF flop
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