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Statistics in Medicine
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September 27, 2002
Monitoring clinical trials: issues and controversies regarding confidentiality
Thomas R Fleming, Susan Ellenberg, David L DeMets
Clinical Trials (London, England)
|
April 10, 2018
Data Monitoring Committees: Current issues
Thomas R Fleming, Susan S Ellenberg, David L DeMets
JAMA
|
February 28, 2020
When Can Intermediate Outcomes Be Used as Surrogate Outcomes?
David L DeMets, Bruce M Psaty, Thomas R Fleming
Biostatistics (Oxford, England)
|
June 22, 2017
Discussion: The role, position, and function of the FDA-The past, present, and future
Thomas R Fleming, David L Demets, Lisa M McShane
Journal of Allergy and Infectious Diseases
|
January 10, 2022
Monitoring clinical trials in infectious diseases
David L DeMets, Thomas R Fleming, Susan S Ellenberg
Journal of Nematology
|
January 23, 2018
Chemosensory Responses of Plant Parasitic Nematodes to Selected Phytochemicals Reveal Long-Term Habituation Traits
Thomas R Fleming, Aaron G Maule, Colin C Fleming
JAMA
|
July 15, 2010
Bias and trials stopped early for benefit
Susan S Ellenberg, David L DeMets, Thomas R Fleming
Clinical Trials (London, England)
|
April 25, 2023
Finding the (biomarker-defined) subgroup of patients who benefit from a novel therapy: No time for a game of hide and seek
Lisa Meier McShane, Mark D Rothmann, Thomas R Fleming
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
May 6, 2009
Issues in using progression-free survival when evaluating oncology products
Thomas R Fleming, Mark D Rothmann, Hong Laura Lu
Science and Engineering Ethics
|
November 25, 2016
Institutional Responsibility and the Flawed Genomic Biomarkers at Duke University: A Missed Opportunity for Transparency and Accountability
David L DeMets, Thomas R Fleming, Gail Geller, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 109) with videos related to
Sort By:
Page
of 11
Statistics in Medicine
|
September 27, 2002
Monitoring clinical trials: issues and controversies regarding confidentiality
Thomas R Fleming, Susan Ellenberg, David L DeMets
Clinical Trials (London, England)
|
April 10, 2018
Data Monitoring Committees: Current issues
Thomas R Fleming, Susan S Ellenberg, David L DeMets
JAMA
|
February 28, 2020
When Can Intermediate Outcomes Be Used as Surrogate Outcomes?
David L DeMets, Bruce M Psaty, Thomas R Fleming
Biostatistics (Oxford, England)
|
June 22, 2017
Discussion: The role, position, and function of the FDA-The past, present, and future
Thomas R Fleming, David L Demets, Lisa M McShane
Journal of Allergy and Infectious Diseases
|
January 10, 2022
Monitoring clinical trials in infectious diseases
David L DeMets, Thomas R Fleming, Susan S Ellenberg
Journal of Nematology
|
January 23, 2018
Chemosensory Responses of Plant Parasitic Nematodes to Selected Phytochemicals Reveal Long-Term Habituation Traits
Thomas R Fleming, Aaron G Maule, Colin C Fleming
JAMA
|
July 15, 2010
Bias and trials stopped early for benefit
Susan S Ellenberg, David L DeMets, Thomas R Fleming
Clinical Trials (London, England)
|
April 25, 2023
Finding the (biomarker-defined) subgroup of patients who benefit from a novel therapy: No time for a game of hide and seek
Lisa Meier McShane, Mark D Rothmann, Thomas R Fleming
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
May 6, 2009
Issues in using progression-free survival when evaluating oncology products
Thomas R Fleming, Mark D Rothmann, Hong Laura Lu
Science and Engineering Ethics
|
November 25, 2016
Institutional Responsibility and the Flawed Genomic Biomarkers at Duke University: A Missed Opportunity for Transparency and Accountability
David L DeMets, Thomas R Fleming, Gail Geller, et al.
Page
of 11