Adaptive patient enrichment designs in therapeutic trials von Wang, Sue‐Jane, James Hung, H. M., O'Neill, Robert T.

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Challenges to multiple testing in clinical trials von James Hung, H. M., Wang, Sue-Jane

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Commentary on "Applying CHW method to 2-in-1 design: gain or lose" von Cui, Lu, Hung, H.M. James, Wang, Sue Jane

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Statistical inference problems in sequential parallel comparison design von Cui, Yifan, Ogbagaber, Semhar, Hung, H.M. James

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Rejoinder to "Statistical inference problems in sequential parallel comparison designs" von Cui, Yifan, Ogbagaber, Semhar, Hung, H.M. James

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Statistical challenges in a regulatory review of cardiovascular and CNS clinical trials von Hung, H. M. James, Wang, Sue-Jane, Yang, Peiling, Jin, Kun, Lawrence, John, Kordzakhia, George, Massie, Tristan

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2017 Cardiovascular and Stroke Endpoint Definitions for Clinical Trials von Hicks, Karen A, Mahaffey, Kenneth W, Mehran, Roxana, Nissen, Steven E, Wiviott, Stephen D, Dunn, Billy, Solomon, Scott D, Marler, John R, Teerlink, John R, Farb, Andrew, Morrow, David A, Targum, Shari L, Sila, Cathy A, Hai, Mary T Thanh, Jaff, Michael R, Joffe, Hylton V, Cutlip, Donald E, Desai, Akshay S, Lewis, Eldrin F, Gibson, C Michael, Landray, Martin J, Lincoff, A Michael, White, Christopher J, Brooks, Steven S, Rosenfield, Kenneth, Domanski, Michael J, Lansky, Alexandra J, McMurray, John J.V, Tcheng, James E, Steinhubl, Steven R, Burton, Paul, Mauri, Laura, O’Connor, Christopher M, Pfeffer, Marc A, Hung, H.M James, Stockbridge, Norman L, Chaitman, Bernard R, Temple, Robert J

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Methods for Employing Information About Uncertainty of Ascertainment of Events in Clinical Trials von Chen, Yiming, Lawrence, John, Hung, H. M. James, Stockbridge, Norman

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Paradigms for adaptive statistical information designs: practical experiences and strategies von Wang, Sue-Jane, James Hung, H. M., O'Neill, Robert

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Ethnic Sensitive or Molecular Sensitive Beyond All Regions Being Equal in Multiregional Clinical Trials von Wang, Sue-Jane, James Hung, H. M.

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A Regulatory View on Adaptive/Flexible Clinical Trial Design von Hung, H. M. James, O'Neill, Robert T., Wang, Sue-Jane, Lawrence, John

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Impacts on type I error rate with inappropriate use of learn and confirm in confirmatory adaptive design trials von Wang, Sue-Jane, James Hung, H. M., O'Neill, Robert T.

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Regulatory Perspectives on Multiplicity in Adaptive Design Clinical Trials throughout a Drug Development Program von Wang, Sue-Jane, James Hung, H. M., O'Neill, Robert

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Establishing consistency across all regions in a multi-regional clinical trial von Tsou, Hsiao-Hui, James Hung, H. M., Chen, Yue-Ming, Huang, Wong-Shian, Chang, Wan-jung, Hsiao, Chin-Fu

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Sample Size Adaptation in Fixed-Dose Combination Drug Trial von James Hung, H. M., Wang, Sue-Jane

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A Regulatory Perspective on Essential Considerations in Design and Analysis of Subgroups When Correctly Classified von Wang, Sue-Jane, Hung, H. M. James

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Assessing Treatment Effects That Capture Disease Burden in Serious Chronic Diseases von Akacha, Mouna, Binkowitz, Bruce, Claggett, Brian, Hung, H. M. James, Mueller-Velten, Guenther, Stockbridge, Norman

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Modification of Sample Size in Group Sequential Clinical Trials von Chi, Lu, Hung, H. M. James, Wang, Sue‐Jane

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Consideration of regional difference in design and analysis of multi-regional trials von Hung, H. M. James, Wang, Sue-Jane, O'Neill, Robert T.

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Some Controversial Multiple Testing Problems in Regulatory Applications von Hung, H. M. James, Wang, Sue-Jane

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