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Statistics in Biopharmaceutical Research Volume 15, 2023 - Issue 2
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Special Section: Estimands, Design and Analysis of Clinical Trials with Time-to-Event Outcomes

Rejoinder to Comments on “Non-Proportional Hazards – An Evaluation of the MaxCombo Test in Cancer Clinical Trials”

Yuan-Li Shena Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDCorrespondence[email protected]
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Sirisha Mushtia Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Flora Mulkeya Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Thomas Gwisea Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Xin Wanga Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Jiaxi Zhoua Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Xin Gaoa Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Shenghui Tanga Office of Biostatistics, Office of Translational Science, CDER, FDA, Silver Spring, MDView further author information
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Marc R. Theoretb Oncology Center for Excellence (OCE), FDA, Silver Spring, MDView further author information
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Richard Pazdurb Oncology Center for Excellence (OCE), FDA, Silver Spring, MDView further author information
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Rajeshwari Sridharab Oncology Center for Excellence (OCE), FDA, Silver Spring, MDView further author information
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Pages 315-317 | Published online: 22 May 2023
 
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Acknowledgments

This article reflects the views of the authors and should not be construed to represent FDA’s views or policies.

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Funding

The author(s) reported there is no funding associated with the work featured in this article.

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