PLX-038 is under clinical development by ProLynx and currently in Phase II for Paraplegia. According to GlobalData, Phase II drugs for Paraplegia does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the PLX-038 LoA Report. 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.
PLX-038 overview
PLX-038 is under development for the treatment of recurrent medulloblastoma, ependymoma, refractory or relapsed solid tumors including squamous non-small cell lung cancer, small cell lung cancer, triple-negative breast cancer (TNBC), ovarian cancer, peritoneal cancer, fallopian tube cancer, primary central nervous system tumor and paraplegia. It is administered through the intravenous route. It is a small molecule, long-acting, pegylated form of SN38. SN-38 is the active metabolite of the anti-cancer agent irinotecan (CPT-11). It acts by targeting topoisomerase 1. The drug candidate is developed based on the disruptive drug delivery system (DDS) technology.
PLX-038 was under development for the treatment of colorectal cancer and gastric cancer.
ProLynx overview
ProLynx is developing peptides, proteins and small molecules for the treatment of cancer. The company is headquartered in San Francisco, California, the US.
For a complete picture of PLX-038’s drug-specific PTSR and LoA scores, buy the report here.
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