Aethlon Medical reports results from in vitro study of Hemopurifier

Aethlon Medical announced positive results from an in vitro binding study of its Hemopurifier in removing extracellular vesicles from plasma. The translational study provides pre-clinical evidence to support Aethlon’s planned phase 1 safety, feasibility and dose-finding clinical trials of the Hemopurifier in patients with solid tumors who have stable or progressive disease during anti-PD-1 monotherapy treatment, such as Keytruda or Opdivo. “The positive data from this in vitro binding study of the Hemopurifier is an important step forward for Aethlon, ahead of the potential start of our planned phase 1 oncology trials in Australia and India,” stated James Frakes, Interim Chief Executive Officer and Chief Financial Officer of Aethlon Medical.