APO-2 is under clinical development by Aposcience and currently in Phase II for Diabetic Foot Ulcers. According to GlobalData, Phase II drugs for Diabetic Foot Ulcers 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 APO-2 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.

APO-2 overview

APO-2 is under development for the treatment of diabetic foot ulcer, contact dermatitis and other chronic dermal wounds. The drug candidate is administered through a cutaneous and topical routes. It is comprised of apoptotic peripheral blood mononuclear cells (APOSEC). These apoptotic cells are derived from peripheral blood mononuclear cells (PBMCs). The drug candidate acts by targeting cytoprotective kinase pathways involved in wound healing.

For a complete picture of APO-2’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.