{"id":389014,"date":"2023-12-20T08:37:50","date_gmt":"2023-12-20T13:37:50","guid":{"rendered":"https:\/\/platohealth.ai\/trends-in-oncology-study-design-from-optimus-to-endpoints\/"},"modified":"2023-12-20T10:43:01","modified_gmt":"2023-12-20T15:43:01","slug":"trends-in-oncology-study-design-from-optimus-to-endpoints","status":"publish","type":"post","link":"https:\/\/platohealth.ai\/trends-in-oncology-study-design-from-optimus-to-endpoints\/","title":{"rendered":"Trends in Oncology Study Design, from Optimus to Endpoints","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"
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In November 2023, at Outsourcing Clinical Trials Dach in Zurich, our Executive Director, Oncology Strategy Lead, Matt Cooper<\/a>, presented \u201cDelivering Oncology Studies \u2013 Challenges and Considerations.\u201d His presentation covered various aspects of oncology clinical programs, focusing on study design trends, with reference to both the recently implemented FDA Project Optimus guidance<\/a> and studies we have seen from sponsors. Among these trends included:<\/p>\n

Randomization<\/strong><\/p>\n

One key trend in oncology study design is a desire from the FDA to, where possible, move away from single-arm trials towards more randomized trials in the earlier setting. A randomized design can help alleviate some of the potential sources of bias in a trial, particularly regarding patient selection at higher doses. For initial dose-finding trials, they do not need to be powered to determine statistical superiority but instead should have sufficient patients to convey the trends between toxicity and dose efficacy.<\/p>\n

There is also a move to take two dose levels out of Phase 1 and into Phase 2 to help define the best tolerated\/effective dose more accurately. If two or more doses are discovered to have comparable efficacy, the lowest effective dose should be used in the registration trial to help minimize the toxicity effects when the drug is used in a broader heterogeneous patient population.<\/p>\n

Biomarker Endpoints<\/strong><\/p>\n

Biomarker endpoints<\/a> are another helpful way to assess the potential efficacy of both initial dose-finding studies and dose-optimization studies. To interpret early clinical data, it\u2019s important to:<\/p>\n