Osiris wins FDA clearance to broaden Prochymal expanded access program
In May 2008, the FDA approved the first Prochymal expanded access program for the treatment of pediatric graft versus host disease (GVHD) patients. Congress and the FDA created
Voro Therapeutics and Alloy Therapeutics have formed a strategic research partnership to develop tumour-selective, next-generation masked T-cell engager (TCE) therapeutics.