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Chengxing Cindy Lu

Showing results (1-10 of 8) with videos related to

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Journal of Biopharmaceutical Statistics|February 16, 2024
Considerations for master protocols using external controlsJie Chen, Xiaoyun Nicole Li, Chengxing Cindy Lu, et al.
Therapeutic Innovation & Regulatory Science|May 3, 2022
Statistical and Operational Considerations for 2-Stage Adaptive Designs with Simultaneous Evaluation of Overall and Marker-Selected Populations in Oncology Confirmatory TrialsWeidong Zhang, Sunhee Ro, Qi Jiang, et al.
Therapeutic Innovation & Regulatory Science|June 23, 2021
Practical Considerations and Recommendations for Master Protocol Framework: Basket, Umbrella and Platform TrialsChengxing Cindy Lu, Xiaoyun Nicole Li, Kristine Broglio, et al.
Therapeutic Innovation & Regulatory Science|May 13, 2023
Statistical Considerations on the Use of RWD/RWE for Oncology Drug Approvals: Overview and Lessons LearnedSunhee K Ro, Weidong Zhang, Qi Jiang, et al.
Therapeutic Innovation & Regulatory Science|August 5, 2025
Ensuring Quality and Interpretability of Progression Free Survival and Overall Survival in Oncology Clinical TrialsPhilip He, Haijun Ma, Chengxing Cindy Lu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 4, 2023
Tumor-Agnostic Approvals: Insights and Practical ConsiderationsChengxing Cindy Lu, Robert A Beckman, Xiaoyun Nicole Li, et al.
Statistics in Biopharmaceutical Research|June 5, 2023
Accuracy and Safety of Novel Designs for Phase I Drug-Combination Oncology TrialsRong Liu, Ying Yuan, Suman Sen, et al.
Therapeutic Innovation & Regulatory Science|August 19, 2025
Company Sponsored Platform Trials: Recommendations and Lessons Learned from Cross-Industry InterviewsYujun Wu, Chengxing Cindy Lu, Mehreteab Aregay, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Biopharmaceutical Statistics|February 16, 2024
Considerations for master protocols using external controlsJie Chen, Xiaoyun Nicole Li, Chengxing Cindy Lu, et al.
Therapeutic Innovation & Regulatory Science|May 3, 2022
Statistical and Operational Considerations for 2-Stage Adaptive Designs with Simultaneous Evaluation of Overall and Marker-Selected Populations in Oncology Confirmatory TrialsWeidong Zhang, Sunhee Ro, Qi Jiang, et al.
Therapeutic Innovation & Regulatory Science|June 23, 2021
Practical Considerations and Recommendations for Master Protocol Framework: Basket, Umbrella and Platform TrialsChengxing Cindy Lu, Xiaoyun Nicole Li, Kristine Broglio, et al.
Therapeutic Innovation & Regulatory Science|May 13, 2023
Statistical Considerations on the Use of RWD/RWE for Oncology Drug Approvals: Overview and Lessons LearnedSunhee K Ro, Weidong Zhang, Qi Jiang, et al.
Therapeutic Innovation & Regulatory Science|August 5, 2025
Ensuring Quality and Interpretability of Progression Free Survival and Overall Survival in Oncology Clinical TrialsPhilip He, Haijun Ma, Chengxing Cindy Lu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 4, 2023
Tumor-Agnostic Approvals: Insights and Practical ConsiderationsChengxing Cindy Lu, Robert A Beckman, Xiaoyun Nicole Li, et al.
Statistics in Biopharmaceutical Research|June 5, 2023
Accuracy and Safety of Novel Designs for Phase I Drug-Combination Oncology TrialsRong Liu, Ying Yuan, Suman Sen, et al.
Therapeutic Innovation & Regulatory Science|August 19, 2025
Company Sponsored Platform Trials: Recommendations and Lessons Learned from Cross-Industry InterviewsYujun Wu, Chengxing Cindy Lu, Mehreteab Aregay, et al.
Pageof 1