Dr. Murat Kalayoglu, CEO at Cartesian Therapeutics, details the cell and gene therapy sector’s advancements in RNA cell therapy and the why behind the company’s decision to build its own wholly-owned GMP manufacturing facility.

The U.S. Food and Drug Administration (FDA) has granted Fast Track designation for STRO-002. The investigational drug, being developed by Sutro Biopharma, is a folate receptor alpha (FolRα)-targeting antibody-drug conjugate (ADC) for the treatment of patients with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior lines of systemic therapy. […]

The FDA has granted a fast track designation to STRO-002 as a potential therapeutic option for patients with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer who have previously received 1 to 3 lines of systemic therapy.1 The folate receptor α (FolRα)–targeting antibody-drug conjugate (ADC) is under examination in the phase 1 STRO-002-GM1 trial […]