PLX-038 is under clinical development by ProLynx and currently in Phase II for Ependymoma. According to GlobalData, Phase II drugs for Ependymoma 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.

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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, colorectal cancer, small cell lung cancer, triple-negative breast cancer (TNBC), ovarian cancer, peritoneal cancer, fallopian tube cancer and gastric cancer. 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.

ProLynx overview

ProLynx is a biotechnology company that has developed advanced linker technologies and a facile, transformative platform for controlled release of therapeutics from circulating and fixed macromolecular conjugates. 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.

This content was updated on 22 April 2024

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.