FDA Clears IND of Intravenous JCXH-21... - Advanced Prostate...

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FDA Clears IND of Intravenous JCXH-211 in Advanced Solid Tumors

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The FDA has granted clearance to an investigational new drug (IND) application of intravenous (IV) JCXH-211 in patients with advanced solid tumors.

JCXH-211 is a first-in-class, self-replicating mRNA (srRNA) encoding the engineered human interleukin (IL)-12 protein.

With this IND, a phase 1/2 study will begin, and investigators will evaluate IV JCXH-211 for the treatment of malignant solid tumors.

Source : targetedonc.com/view/fda-cl...

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