CLINICAL BIOLOGICS MANUFACTURING AND CELL CULTURE (CBMCC) SHARED RESOURCE Timothy Clay, Ph.D., Director The Cancer Center Clinical Biologics Manufacturing and Cell Culture (CBMCC) Shared Resource combines hree elements: (i) the Clinical Biologics Manufacturing Unit for manufacturing under cGMP cellular, tissue, _rotein, antibody, nucleic acid, and viral vector modified biologics for testing in early phase clinical trials; (ii) ihe Non-clinical Cell Culture Unit which is a specialized cell culture service that includes a cell line repository and large scale cell culture capacity for Cancer Center investigators; and (iii) the Supply Unit, a self-supporting reagent supply service for research laboratories within the Cancer Center and campus-wide. The Clinical Biologics Manufacturing Unit is a new addition to this shared resource since the previous review in 1998. By adding this new component to this shared resource, we have greatly increased the scientific merit of the shared resource and established a critical element within the Cancer Center for translating novel therapies from the research bench to early phase clinical trials. The Unit provides a skilled staff with extensive technica!, expertise in clinical biologics manufacturing under strictly regulated, FDA approved protocols and SOP s, who can perform manufacturing for Cancer Center members. Additionally, regulatory submission s to the IRB, FDA, CTEP, and NIH-RAC, and regulatory oversight of manufacturing is also supported within this Unit. The non-clinical Cell Culture Unit provides technical support for the Cancer Center members. In 2003 the Unit provided services to 97 peer-reviewed Cancer Center members in all 11 Cancer Center Programs. Many Cancer Center members rely on this Unit to perform small and large-scale cell culture because they lack the personnel, expertise, or the equipment to perform this task in their own labs. The Supply Unit provides material support for CMBCC technical efforts and for the Cancer Center member's own labs. Its large user base allows it to negotiate excellent price contracts (75% discounts) and pass these savings directly on to Cancer Center members.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014236-34
Application #
7726668
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-01-01
Budget End
2008-12-31
Support Year
34
Fiscal Year
2008
Total Cost
$126,471
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Dai, Ziwei; Mentch, Samantha J; Gao, Xia et al. (2018) Methionine metabolism influences genomic architecture and gene expression through H3K4me3 peak width. Nat Commun 9:1955
Powell Gray, Bethany; Kelly, Linsley; Ahrens, Douglas P et al. (2018) Tunable cytotoxic aptamer-drug conjugates for the treatment of prostate cancer. Proc Natl Acad Sci U S A 115:4761-4766
Abdi, Khadar; Lai, Chun-Hsiang; Paez-Gonzalez, Patricia et al. (2018) Uncovering inherent cellular plasticity of multiciliated ependyma leading to ventricular wall transformation and hydrocephalus. Nat Commun 9:1655
Hudson, Kathryn E; Rizzieri, David; Thomas, Samantha M et al. (2018) Dose-intense chemoimmunotherapy plus radioimmunotherapy in high-risk diffuse large B-cell lymphoma and mantle cell lymphoma: a phase II study. Br J Haematol :
Fayanju, Oluwadamilola M; Park, Ko Un; Lucci, Anthony (2018) Molecular Genomic Testing for Breast Cancer: Utility for Surgeons. Ann Surg Oncol 25:512-519
Porter, Laura S; Fish, Laura; Steinhauser, Karen (2018) Themes Addressed by Couples With Advanced Cancer During a Communication Skills Training Intervention. J Pain Symptom Manage 56:252-258
Káradóttir, Ragnhildur T; Kuo, Chay T (2018) Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis. Annu Rev Neurosci 41:139-161
Han, Peng; Liu, Hongliang; Shi, Qiong et al. (2018) Associations between expression levels of nucleotide excision repair proteins in lymphoblastoid cells and risk of squamous cell carcinoma of the head and neck. Mol Carcinog 57:784-793
Xu, Yinghui; Wang, Yanru; Liu, Hongliang et al. (2018) Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival. Mol Carcinog 57:22-31
Abdi, Khadar; Kuo, Chay T (2018) Laminating the mammalian cortex during development: cell polarity protein function and Hippo signaling. Genes Dev 32:740-741

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