Stopped: Due to a Dose Limiting Toxicity in another sister trial with same technology.
This is a Phase 1/2, open-label, multicenter, non-randomized study to investigate the safety, tolerability, and clinical activity of HER2-specific dual-switch CAR-T cells, BPX-603, administered with rimiducid to subjects with previously treated, locally advanced or metastatic solid tumors which are HER2 amplified/overexpressed.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Proportion of subjects experiencing Dose Limiting Toxicities at increasing doses of BPX-603
Timeframe: 35 days from time of BPX-603 infusion
Maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE)
Timeframe: through Phase 1 completion, up to 2 years