ProBio and Curocell Reach Major CAR‑T Commercialization Milestone
Bringing next-generation therapies to patients requires more than manufacturing capacity. It demands a CDMO with proven regulatory, technical, and commercial execution.
September 29, 2026
ProBio demonstrated this by supporting Curocell’s CAR-T programme from post-IND transfer through BLA approval and commercial manufacturing, achieving first-pass validation success and regulatory approval.
Backed by deep expertise in plasmid DNA, viral vectors, process development, and GMP manufacturing, ProBio helps innovators de-risk development, accelerate timelines, and build a stronger pathway to clinical and commercial success in in vivo CAR-T.
Published: September 29, 2026
