Original language | English (US) |
---|---|
Pages (from-to) | 405-415 |
Number of pages | 11 |
Journal | Clinical Trials |
Volume | 20 |
Issue number | 4 |
DOIs |
|
State | Published - Aug 2023 |
ASJC Scopus subject areas
- Pharmacology
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In: Clinical Trials, Vol. 20, No. 4, 08.2023, p. 405-415.
Research output: Contribution to journal › Comment/debate › peer-review
}
TY - JOUR
T1 - 14th Annual University of Pennsylvania Conference on statistical issues in clinical trials/subgroup analysis in clinical trials
T2 - Opportunities and challenges (afternoon panel discussion)
AU - Imai, Kosuke
AU - Rosenblum, Michael
AU - Rothmann, Mark
N1 - Funding Information: The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: M.R. was supported by the Johns Hopkins Center of Excellence in Regulatory Science and Innovation, which is funded by the Food and Drug Administration (FDA) of the U.S. Department of Health and Human Services (HHS) as part of a financial assistance award (grant no. U01FD005942). The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by any of the aforementioned organizations, the FDA/HHS, nor the U.S. Government. The other author(s) declared no receipt of financial support for the research, authorship, and/or publication of this article. Funding Information: The authors thank their professional society sponsors the Society for Clinical Trials, the American Statistical Association, and the National Institute of Statistical Sciences whose structural support has been invaluable for the success of this conference. Members of the program committee include Drs Susan S. Ellenberg, Jonas H. Ellenberg, Mary Putt, Pam Shaw (currently at Kaiser Permanente Washington Health Research Institute), Alisa J. Stephens-Shields, and James Lewis in the Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania. The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: M.R. was supported by the Johns Hopkins Center of Excellence in Regulatory Science and Innovation, which is funded by the Food and Drug Administration (FDA) of the U.S. Department of Health and Human Services (HHS) as part of a financial assistance award (grant no. U01FD005942). The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by any of the aforementioned organizations, the FDA/HHS, nor the U.S. Government. The other author(s) declared no receipt of financial support for the research, authorship, and/or publication of this article.
PY - 2023/8
Y1 - 2023/8
UR - http://www.scopus.com/inward/record.url?scp=85159000793&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85159000793&partnerID=8YFLogxK
U2 - 10.1177/17407745231169681
DO - 10.1177/17407745231169681
M3 - Comment/debate
C2 - 37148213
AN - SCOPUS:85159000793
SN - 1740-7745
VL - 20
SP - 405
EP - 415
JO - Clinical Trials
JF - Clinical Trials
IS - 4
ER -