Protocol Review and Monitoring System (PRMS) The Perlmutter Cancer Center (PCC) Protocol Review and Monitoring System (PRMS), internally known as the Protocol Review and Monitoring Committee (PRMC), reviews all cancer-related clinical research under the jurisdiction of PCC and NYU Langone Health (NYULH). The objectives of the PRMC are to determine whether a protocol is scientifically and statistically sound, appropriately designed, feasible and not competitive with other ongoing studies at PCC. The PRMC also determines if protocols are aligned with PCC scientific priorities and the needs of our catchment area, evaluates whether accrual goals are realistic, and assesses the likelihood of trial completion. The PRMC has the ultimate authority to approve and prioritize, in an efficient and timely manner, the activation of cancer-related protocols that have a high level of scientific merit and meet the scientific priorities of the PCC. The PRMC also decides whether to terminate protocols that do not demonstrate acceptable progress. Investigator-initiated studies are reviewed for progress at least bi-annually, and other studies annually. All studies are reviewed more frequently if deemed necessary by the PRMC, due to low accrual or if protocol amendments significantly change the scientific design or accrual targets of the protocol. The PRMC is also charged with ensuring that all cancer-related clinical research at NYULH meets appropriate criteria for inclusion of women, minorities and children. The PRMC is fully integrated into the clinical trials review and approval systems of NYULH. In this context, it functions in a well-coordinated, expeditious, but non-overlapping manner with the NYULH IRB, Office of Science and Research (OSR), and various other NYULH review entities, including Environmental Health and Radiation Safety, Biosafety, and Investigational Pharmacy. Consistent with the Institutional agreement with the NCI, the NYULH IRB will not grant full approval to any cancer-related human subjects protocol without receiving documentation of PRMC approval.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016087-40
Application #
10124337
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-12-01
Project End
2024-02-29
Budget Start
2021-03-01
Budget End
2022-02-28
Support Year
40
Fiscal Year
2021
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Snetkova, Valentina; Skok, Jane A (2018) Enhancer talk. Epigenomics 10:483-498
Litwinoff, Evelyn M S; Gold, Merav Y; Singh, Karan et al. (2018) Myeloid ATG16L1 does not affect adipose tissue inflammation or body mass in mice fed high fat diet. Obes Res Clin Pract 12:174-186
Lee, Chul-Hwan; Holder, Marlene; Grau, Daniel et al. (2018) Distinct Stimulatory Mechanisms Regulate the Catalytic Activity of Polycomb Repressive Complex 2. Mol Cell 70:435-448.e5
Fan, Xiaozhou; Alekseyenko, Alexander V; Wu, Jing et al. (2018) Human oral microbiome and prospective risk for pancreatic cancer: a population-based nested case-control study. Gut 67:120-127
Gregory, Ann C; Sullivan, Matthew B; Segal, Leopoldo N et al. (2018) Smoking is associated with quantifiable differences in the human lung DNA virome and metabolome. Respir Res 19:174
Taylor, Martin S; Altukhov, Ilya; Molloy, Kelly R et al. (2018) Dissection of affinity captured LINE-1 macromolecular complexes. Elife 7:
Bertrand, Anne; Baron, Maria; Hoang, Dung M et al. (2018) In Vivo Evaluation of Neuronal Transport in Murine Models of Neurodegeneration Using Manganese-Enhanced MRI. Methods Mol Biol 1779:527-541
Jung, Seungyoun; Allen, Naomi; Arslan, Alan A et al. (2018) Anti-Müllerian hormone and risk of ovarian cancer in nine cohorts. Int J Cancer 142:262-270
Wang, Sophia S; Carrington, Mary; Berndt, Sonja I et al. (2018) HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes. Cancer Res 78:4086-4096
Kirkling, Margaret E; Cytlak, Urszula; Lau, Colleen M et al. (2018) Notch Signaling Facilitates In Vitro Generation of Cross-Presenting Classical Dendritic Cells. Cell Rep 23:3658-3672.e6

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