reMYND has a proprietary phenotypic screening platform to discover disease-modifying small molecule treatments and their novel target and MoA to counteract the toxicity induced by misfolded proteins, such as Tau for AD or Synuclein for PD. We validate and optimize our leads in our proprietary cellular assays and animal models. In addition, we can identify the corresponding novel drug target and its mode-of-action through a multitude of assays such as three-hybrid screening.