“We are pleased that MT-101 has received Fast Track designation from the FDA,” said Michele Gerber, MD, MPH, Chief Medical Officer of Myeloid. “The designation speaks to the serious nature of CD5+ relapsed/refractory PTCL , an aggressive form of non-Hodgkin lymphoma, and the potential MT-101 has to transform the treatment paradigm of this disease. IMAGINE, a Phase 1/2 trial assessing safety, tolerability, and efficacy of MT-101 in this indication is open for enrollment and the initial data is very encouraging.”
