AdAPT-001 is under clinical development by EpicentRx and currently in Phase II for Chordoma. According to GlobalData, Phase II drugs for Chordoma 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 AdAPT-001 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.

AdAPT-001 overview

AdAPT-001 is under development for the treatment of malignant solid tumor, leiomyosarcoma, chondrosarcoma, triple-negative breast cancer, chordoma and liver metastases in metastatic colorectal cancer (mCRC). The therapeutic candidate is a replication competent adenovirus type-5 carrying a TGF-beta trap transgene. It is developed based on Adaptigene oncolytic virus platform. It is administered through intratumor route and hepatic artery infusion. The drug candidate is adenovirus viral vector.

EpicentRx overview

EpicentRx is a biopharmaceutical company that carries out the development of novel therapies aimed at targeting cancer and chronic diseases. The company’s main products include the PRETECT Platform, featuring the Phase 3 investigational product RRx-001, and the AdAPT Platform, with its lead clinical stage candidate AdAPT-001. EpicentRx has developed the proprietary eLoop device, designed for optimized delivery of intravenous treatments. The company’s products are intended for use in the pharmaceutical industry, specifically for the treatment of various forms of cancer and chronic inflammatory diseases. The company operates in the US and China. EpicentRx is headquartered in La Jolla, California, the US.

For a complete picture of AdAPT-001’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 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.