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JAMA
|
March 23, 2026
Reflections on FDA Draft Guidance on Bayesian Methods in Trials-Protecting Scientific Integrity and Evidentiary Standards
Scott R Evans, Thomas R Fleming, Holly Janes, et al.
Drug Information Journal
|
June 23, 2012
Testing in a Prespecified Subgroup and the Intent-to-Treat Population
Mark D Rothmann, Jenny J Zhang, Laura Lu, et al.
Journal of Biopharmaceutical Statistics
|
June 14, 2014
Enhancing trial integrity by protecting the independence of data monitoring committees in clinical trials
Thomas R Fleming, Charles H Hennekens, Marc A Pfeffer, et al.
Biometrics
|
March 23, 2011
Insights on the robust variance estimator under recurrent-events model
Hussein R Al-Khalidi, Yili Hong, Thomas R Fleming, et al.
Clinical Trials (London, England)
|
August 13, 2011
Some essential considerations in the design and conduct of non-inferiority trials
Thomas R Fleming, Katherine Odem-Davis, Mark D Rothmann, et al.
The Journal of Infectious Diseases
|
April 21, 2022
Reliably Assessing Duration of Protection for Coronavirus Disease 2019 Vaccines
Dan-Yu Lin, Donglin Zeng, Yu Gu, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)
|
June 15, 2013
Study design considerations for evaluating efficacy of systemic preexposure prophylaxis interventions
Deborah Donnell, James P Hughes, Lei Wang, et al.
Lancet (London, England)
|
August 31, 2020
COVID-19 vaccine trials should seek worthwhile efficacy
Philip Krause, Thomas R Fleming, Ira Longini, et al.
Lancet (London, England)
|
October 30, 2020
Maintaining confidentiality of emerging results in COVID-19 vaccine trials is essential
Philip R Krause, Thomas R Fleming, Susan S Ellenberg, et al.
Clinical Trials (London, England)
|
April 1, 2008
Maintaining confidentiality of interim data to enhance trial integrity and credibility
Thomas R Fleming, Katrina Sharples, John McCall, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 109) with videos related to
Sort By:
Page
of 11
JAMA
|
March 23, 2026
Reflections on FDA Draft Guidance on Bayesian Methods in Trials-Protecting Scientific Integrity and Evidentiary Standards
Scott R Evans, Thomas R Fleming, Holly Janes, et al.
Drug Information Journal
|
June 23, 2012
Testing in a Prespecified Subgroup and the Intent-to-Treat Population
Mark D Rothmann, Jenny J Zhang, Laura Lu, et al.
Journal of Biopharmaceutical Statistics
|
June 14, 2014
Enhancing trial integrity by protecting the independence of data monitoring committees in clinical trials
Thomas R Fleming, Charles H Hennekens, Marc A Pfeffer, et al.
Biometrics
|
March 23, 2011
Insights on the robust variance estimator under recurrent-events model
Hussein R Al-Khalidi, Yili Hong, Thomas R Fleming, et al.
Clinical Trials (London, England)
|
August 13, 2011
Some essential considerations in the design and conduct of non-inferiority trials
Thomas R Fleming, Katherine Odem-Davis, Mark D Rothmann, et al.
The Journal of Infectious Diseases
|
April 21, 2022
Reliably Assessing Duration of Protection for Coronavirus Disease 2019 Vaccines
Dan-Yu Lin, Donglin Zeng, Yu Gu, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)
|
June 15, 2013
Study design considerations for evaluating efficacy of systemic preexposure prophylaxis interventions
Deborah Donnell, James P Hughes, Lei Wang, et al.
Lancet (London, England)
|
August 31, 2020
COVID-19 vaccine trials should seek worthwhile efficacy
Philip Krause, Thomas R Fleming, Ira Longini, et al.
Lancet (London, England)
|
October 30, 2020
Maintaining confidentiality of emerging results in COVID-19 vaccine trials is essential
Philip R Krause, Thomas R Fleming, Susan S Ellenberg, et al.
Clinical Trials (London, England)
|
April 1, 2008
Maintaining confidentiality of interim data to enhance trial integrity and credibility
Thomas R Fleming, Katrina Sharples, John McCall, et al.
Page
of 11