Simcha Therapeutics signs license agreement with Janssen for DR-18
The deal, facilitated by Johnson & Johnson Innovation, will enable Janssen to develop cell therapies that are armed with DR-18 of Simcha. Janssen will be responsible for the
The US Food and Drug Administration (FDA) has issued a complete response letter (CRL) to Replimune Group’s biologics licence application (BLA) concerning the RP1 therapy in combination with nivolumab for advanced melanoma.
This partnership covers drug-linker technology and CRDMO services right from discovery to commercialisation. WuXi XDC CEO Dr. Jimmy Li said, “IntoCell’s unique drug-linker technologies and our leading, open-access