JCXH-211 is under clinical development by Immorna Hangzhou Biotechnology and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 69% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how JCXH-211’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
JCXH-211 overview
JCXH-211 is under development for the treatment of malignant solid tumor, head and neck cancer, liver cancer, melanoma, triple-negative breast cancer, esophageal cancer, high-grade glioma. The drug candidate is a lipid nanoparticle (LNP) encapsulated self-replicating mRNA encoding the human interleukin 12 (IL12) protein. It is administered by intratumor and intravenous route as injection. It is being developed based on self-replicating RNA (srRNA) technology platform. It was also under development for glioblastoma multiforme.
Immorna Hangzhou Biotechnology overview
Immorna Hangzhou Biotechnology is a biotechnology company focused on the research and development of RNA-based therapeutics and vaccines. The company is headquartered in Hangzhou, Zhejiang, China.
For a complete picture of JCXH-211’s drug-specific PTSR and LoA scores, buy the report here.
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