Multiple Co-primary Endpoints: Medical and Statistical Solutions: A Report from the Multiple Endpoints Expert Team of the Pharmaceutical Research and Manufacturers of America

Author:

Offen Walter,Chuang-Stein Christy,Dmitrienko Alex,Littman Gary,Maca Jeff,Meyerson Laura,Muirhead Robb,Stryszak Paul,Baddy Alex,Chen Kun,Copley-Merriman Kati,Dere Willard,Givens Sam,Hall David,Henry David,Jackson Joseph D.,Krishen Alok,Liu Thomas,Ryder Steve,Sankoh A. J.,Wang Julia,Yeh Chyon-Hwa

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Drug guides,Pharmacology (nursing)

Reference28 articles.

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2. Sankoh AJ, Huque MF, Dubey SD. Some comments on frequently used multiple endpoint adjustment methods in clinical trials. Stat Med. 1997;16:2529–2542.

3. ICH E9. Statistical Principles for Clinical Trials. Step 5 guidance document, 2000. Available at: http://www.ich.org. Accessed November 11, 2006.

4. CPMP/EWP/908/99. Points to consider on multiplicity issues in clinical trials (adopted September 2002). Available at: http://www.emea.cu.int/pdfs/human/ewp/090899en.pdf. Accessed November 11, 2006.

5. Berger RL, Multiparameter hypothesis testing and acceptance sampling. Technometrics. 1982; 24:295–300.

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