Gian-Andrea Thanei, Gaëlle Klingelschmitt, Claude Berge, Hans Ulrich Burger
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引用次数: 0
Abstract
Futility interim analyses remain a topic of anxiety for most clinical drug development teams. While they can significantly reduce the risk involved in the development of innovative therapies and do so at a minimal cost, they are not used frequently enough. Development teams often shy away due to the fear of terminating a potentially successful therapy by mistake. We believe these risks are overestimated and hence necessitate a simple and effective communication to be better understood. The planning of futilities often evolves into complex statistical modeling exercises where various scenarios are simulated and multiple risk metrics are calculated. To assist teams in such discussions we propose a straightforward strategy for establishing a range for the futility threshold and an intuitive futility risk measure to evaluate the associated risks.
期刊介绍:
Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health.
The focus areas of the journal are as follows:
Biostatistics
Clinical Trials
Product Development and Innovation
Global Perspectives
Policy
Regulatory Science
Product Safety
Special Populations