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Journal of Biopharmaceutical Statistics
|
February 26, 2010
Missing data in biologic oncology products
Mark D Rothmann, Kallappa Koti, Kyung Yul Lee, et al.
Journal of Biopharmaceutical Statistics
|
August 21, 2013
Evaluating and adjusting for premature censoring of progression-free survival
Mark Rothmann, Kallappa Koti, Kyung Yul Lee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 5, 2008
U.S. Food and Drug Administration approval: panitumumab for epidermal growth factor receptor-expressing metastatic colorectal carcinoma with progression following fluoropyrimidine-, oxaliplatin-, and irinotecan-containing chemotherapy regimens
Ruthann M Giusti, Kaushikkumar Shastri, Anne M Pilaro, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 11, 2012
U.S. Food and Drug Administration approval summary: brentuximab vedotin for the treatment of relapsed Hodgkin lymphoma or relapsed systemic anaplastic large-cell lymphoma
R Angelo de Claro, Karen McGinn, Virginia Kwitkowski, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Journal of Biopharmaceutical Statistics
|
February 26, 2010
Missing data in biologic oncology products
Mark D Rothmann, Kallappa Koti, Kyung Yul Lee, et al.
Journal of Biopharmaceutical Statistics
|
August 21, 2013
Evaluating and adjusting for premature censoring of progression-free survival
Mark Rothmann, Kallappa Koti, Kyung Yul Lee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 5, 2008
U.S. Food and Drug Administration approval: panitumumab for epidermal growth factor receptor-expressing metastatic colorectal carcinoma with progression following fluoropyrimidine-, oxaliplatin-, and irinotecan-containing chemotherapy regimens
Ruthann M Giusti, Kaushikkumar Shastri, Anne M Pilaro, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 11, 2012
U.S. Food and Drug Administration approval summary: brentuximab vedotin for the treatment of relapsed Hodgkin lymphoma or relapsed systemic anaplastic large-cell lymphoma
R Angelo de Claro, Karen McGinn, Virginia Kwitkowski, et al.
Page
of 1