On May 12th, RemeGen Co., Ltd. (688331.SH/9995.HK) announced that the Clinical Trial Application (CTA) for its novel ADC Drug RC278 has been submitted recently and accepted by National Medical Products Administration (NMPA) Center for Drug Reevaluation (CDE) on May 8th.
RC278, independently designed and developed by RemeGen, emerges as a potentially First-in-Class/Best-in-Class ADC molecule. RC278 can specifically recognize a new tumor target and contains an innovative linker-cytotoxicity system, showing broad-spectrum antitumor activity, manageable safety and pharmacokinetic characteristics in the pre-clinical study.
As an important drug candidate in RemeGen’s ADC pipeline, RC278 boasts unique target and differentiated molecule design, demonstrating RemeGen’s progress in ADC technology. RC278 will bring new treatment option for the advanced solid tumor patients.
