Designs for phase II trials with trade-of between efficacy and toxicity
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Publication:3511752
zbMATH Open1141.62092MaRDI QIDQ3511752FDOQ3511752
Authors: Menggan Yu, Constantin T. Yiannoutsos
Publication date: 11 July 2008
Recommendations
- Incorporating Toxicity Considerations Into the Design of Two-Stage Phase II Clinical Trials
- Treatment Comparisons Based on Two‐Dimensional Safety and Efficacy Alternatives in Oncology Trials
- On construction of single-arm two-stage designs with consideration of both response and toxicity
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Efficient designs for phase II oncology trials with ordinal outcome
Parametric hypothesis testing (62F03) Applications of statistics to biology and medical sciences; meta analysis (62P10) Sequential statistical design (62L05)
Cited In (9)
- Treatment Comparisons Based on Two‐Dimensional Safety and Efficacy Alternatives in Oncology Trials
- Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
- On construction of single-arm two-stage designs with consideration of both response and toxicity
- Phase 2 and 3 Combination Designs to Accelerate Drug Development
- Two-stage phase II trials with early stopping for effectiveness and safety as well as ineffectiveness or harm
- Incorporating Toxicity Considerations Into the Design of Two-Stage Phase II Clinical Trials
- A hybrid geometric phase II/III clinical trial design based on treatment failure time and toxicity
- Efficient designs for phase II oncology trials with ordinal outcome
- Optimal designs for active controlled dose-finding trials with efficacy-toxicity outcomes
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