IOV-1042 is under clinical development by IconOVir Bio and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how IOV-1042’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.

IOV-1042 overview

IOV-1042 is under development for the treatment of solid tumors. It is a chimeric oncolytic Adenovirus (Ad) and administered through intravenous route.

IconOVir Bio overview

IconOVir Bio is a preclinical-stage biotechnology company, engaged in the development of oncolytic virus therapy to improve the treatment of patients with cancer. IconOVir Bio is headquartered in San Diego, California, the US.

For a complete picture of IOV-1042’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.