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Journal of Biopharmaceutical Statistics Volume 22, 2012 - Issue 4: Adaptive Designs for Clinical Trials: Considerations about and Beyond the FDA Adaptive Designs Guidance
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Original Articles

Estimation of Treatment Effect Following a Clinical Trial with Adaptive Design

Xiaolong Luo Celgene Corporation, Summit, New Jersey, USA; University of Medicine and Dentistry of New Jersey, New Jersey, USACorrespondence[email protected]
,
Mingyu Li Celgene Corporation, Summit, New Jersey, USA
,
Weichung Joe Shih University of Medicine and Dentistry of New Jersey, New Jersey, USA
&
Peter Ouyang Celgene Corporation, Summit, New Jersey, USA
Pages 700-718 | Received 16 Dec 2010, Accepted 16 Feb 2012, Published online: 31 May 2012

Citations (5)

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Read on this site (1)

Weichung Joe Shih, Yunqi Zhao & Tai Xie. (2023) Modified Simon’s Two-Stage Design for Phase IIA Clinical Trials in Oncology—Dynamic Monitoring and More Flexibility. Statistics in Biopharmaceutical Research 15:4, pages 838-844.
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Articles from other publishers (4)

David S. Robertson, Babak Choodari‐Oskooei, Munya Dimairo, Laura Flight, Philip Pallmann & Thomas Jaki. (2022) Point estimation for adaptive trial designs I: A methodological review. Statistics in Medicine 42:2, pages 122-145.
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Arsénio Nhacolo & Werner Brannath. (2018) Interval and point estimation in adaptive Phase II trials with binary endpoint. Statistical Methods in Medical Research 28:9, pages 2635-2648.
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Kevin Kunzmann, Laura Benner & Meinhard Kieser. (2017) Point estimation in adaptive enrichment designs. Statistics in Medicine 36:25, pages 3935-3947.
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Lawrence M. Friedman, Curt D. Furberg, David L. DeMets, David M. Reboussin & Christopher B. GrangerLawrence M. Friedman, Curt D. Furberg, David L. DeMets, David M. Reboussin & Christopher B. Granger. 2015. Fundamentals of Clinical Trials. Fundamentals of Clinical Trials 373 401 .

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