MedPacto says U.S. FDA approves additional dose in Phase 2 osteosarcoma trial
MedPacto announced on the 19th that it received approval from the U.S. Food and Drug Administration (FDA) for an Investigational New Drug (IND) protocol amendment to add a medium-dose patient cohort in the Phase 2 clinical trial of Vactosertib, a treatment for osteosarcoma, a rare bone cancer.
The clinical trial is currently underway simultaneously in South..