OR-502 is under clinical development by OncoResponse and currently in Phase II for Ovarian Cancer. According to GlobalData, Phase II drugs for Ovarian Cancer have a 26% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how OR-502’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.
OR-502 overview
OncoResponse overview
OncoResponse is an immuno-oncology company. It discovers, develops and commercializes novel antibodies against cancer by using a human antibody platform. The company’s pipeline products include OR2805 a reprogrammed tumor-associated macrophage and myeloid-derived suppressor cell; OR641 inhibits myeloid and lymphoid checkpoint; OR502 acts as reverse immunosuppression and reprograms tumor-associated macrophage; TME 2.0 is interrogate B-cell repertoire for mAb candidates. It works in partnership with MD Anderson Cancer Center and Theraclone Sciences. OncoResponse is headquartered in Seattle, Washington, the US.
For a complete picture of OR-502’s drug-specific PTSR and LoA scores, buy the report here.
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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.
