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FDA Approval Summary: Axicabtagene Ciloleucel for Relapsed or Refractory Large B-cell Lymphoma
Clinical cancer research, 2019-03, Vol.25 (6), p.1702-1708
2019
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FDA Approval Summary: Brexucabtagene Autoleucel for Treatment of Adults With Relapsed or Refractory B-Cell Precursor Acute Lymphoblastic Leukemia
The oncologist (Dayton, Ohio), 2022-10, Vol.27 (10), p.892-899
2022
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FDA Approval Summary: Axicabtagene Ciloleucel for Relapsed or Refractory Follicular Lymphoma
The oncologist (Dayton, Ohio), 2022-07, Vol.27 (7), p.587-594
2022
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Patient-Reported Outcomes in Pediatric Cancer Registration Trials: A US Food and Drug Administration Perspective
JNCI : Journal of the National Cancer Institute, 2022-01, Vol.114 (1), p.12-19
2022
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Patient-Reported Outcomes in Pediatric Cancer Registration Trials: A US Food and Drug Administration Perspective
JNCI : Journal of the National Cancer Institute, 2021-04, Vol.114 (1)
2021
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Patient-Reported Outcomes in Pediatric Cancer Registration Trials: A US Food and Drug Administration Perspective
JNCI : Journal of the National Cancer Institute, 2021-04, Vol.114 (1)
2021
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2017-2018 Hematology Drug Approvals at the Food and Drug Administration (FDA): Communication of Patient-Reported Outcomes (PRO) Information in FDA Clinical Reviews and Prescribing Information (PI)
Blood, 2019-11, Vol.134 (Supplement_1), p.3450-3450
2019
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A U.S. Food and Drug Administration Age Based Pooled Analysis of Cytokine Release Syndrome and Neurotoxicity in Subjects with Relapsed/Refractory Lymphoma Treated with Chimeric Antigen Receptor (CAR) T Cell Therapy
Blood, 2018-11, Vol.132 (Supplement 1), p.4201-4201
2018
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Paediatric Strategy Forum for medicinal product development of chimeric antigen receptor T-cells in children and adolescents with cancer: ACCELERATE in collaboration with the European Medicines Agency with participation of the Food and Drug Administration
European journal of cancer (1990), 2022-01, Vol.160, p.112-133
2022
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Paediatric Strategy Forum for medicinal product development of chimeric antigen receptor T-cells in children and adolescents with cancer: ACCELERATE in collaboration with the European Medicines Agency with participation of the Food and Drug Administration2
European journal of cancer (1990), 2022-01, Vol.160, p.112
2022
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Paediatric Strategy Forum for medicinal product development of chimeric antigen receptor T-cells in children and adolescents with cancer
European journal of cancer (1990), 2022-01, Vol.160, p.112-133
2022
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Inhibition of STAT1 modulates GVHD after allogeneic BMT through induction of S100A8/A9 (169.38)
The Journal of immunology (1950), 2011-04, Vol.186 (1_Supplement), p.169-169.38
2011
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Dipeptidyl Peptidase Inhibition Alters Myeloid Derived Suppressor Cell Phenotype and Induces Regression of Pediatric Sarcomas
Blood, 2010-11, Vol.116 (21), p.3792-3792
2010
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A pan-inhibitor of DASH family enzymes induces immune-mediated regression of murine sarcoma and is a potent adjuvant to dendritic cell vaccination and adoptive T-cell therapy
Journal of immunotherapy (1997), 2013-10, Vol.36 (8), p.400
2013
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Abstract 1332: Pediatric sarcomas are infiltrated with myeloid derived suppressive cells
Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.1332-1332
2010
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Outreach to immigrant communities: teaching pediatric residents about access to health care
Journal of health care for the poor and underserved, 2007-08, Vol.18 (3), p.510-515
2007
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