The proposed Drug Development Shared Resource is designed to facilitated preclinical drug development leading to selection of new agents for clinical trial. It is composed of two sections, one devoted to preclinical Toxicology. The Preclinical Pharmacology Section, headed by Dr. Bernacki, will evaluate, using human in vitro and in vivo tumor model systems, the biological and therapeutic activity of potential anti- tumor agents and treatments, derived as a result of research being carried out by investigators in the CCSG Programs, or if relevant to the Institute's goals, from outside sources. Based on information regarding the activity and mechanism of action of thee new compounds, combinations of agents (e.g., polyamine analogs and inhibitors) or treatments (e.g., anti-angiogenic chemotherapy and photodynamic therapy) will also be evaluated. Preclinical pharmacological studies will be performed to assess both pharmacokinetic parameters and drug metabolism. The Preclinical Toxicology Section of this Resource, headed drugs and treatments. The primary service provided will be the preclinical toxicologic evaluation of new agents or treatments in rats and dogs. All studies will be conducted under strict adherence to the Good Laboratory Practices (GLP) of the U.S. Food and Drug Administration (FDA). This Resource is capable of conducting all of the experimental and regulatory work necessary and sufficient for IND applications to the FDA prior to initial (Phase I and Phase I/II) clinical trials of new anti-cancer drugs in humans. The scope of these preclinical therapeutic and preclinical toxicology core resource activities forms an integral part of Roswell Park Cancer Institute Corporation's (RPCI) strategy for anti-cancer drug development, aiding in the design of new protocols for clinical trial. Both sections of the Drug Development Resource are available to all RPCI researchers with a need for services, and priority access is given to investigators with peer-reviewed funding. Final decisions regarding prioritization of projects is made my the Chemotherapy Strategy Committee.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016056-25
Application #
6405343
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
1983-12-01
Project End
2002-04-30
Budget Start
Budget End
Support Year
25
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Irons, Eric E; Lau, Joseph T Y (2018) Systemic ST6Gal-1 Is a Pro-survival Factor for Murine Transitional B Cells. Front Immunol 9:2150
Chen, George L; Hahn, Theresa; Wilding, Gregory E et al. (2018) Reduced-Intensity Conditioning with Fludarabine, Melphalan, and Total Body Irradiation for Allogeneic Hematopoietic Cell Transplantation: The Effect of Increasing Melphalan Dose on Underlying Disease and Toxicity. Biol Blood Marrow Transplant :
Khoury, Thaer; Gaudioso, Carmelo; Fang, Yisheng V et al. (2018) The role of skin ulceration in breast carcinoma staging and outcome. Breast J 24:41-50
Griffiths, Elizabeth A; Srivastava, Pragya; Matsuzaki, Junko et al. (2018) NY-ESO-1 Vaccination in Combination with Decitabine Induces Antigen-Specific T-lymphocyte Responses in Patients with Myelodysplastic Syndrome. Clin Cancer Res 24:1019-1029
Hanif, Ahmad; Wang, Eunice S; Thompson, James E et al. (2018) Combining blinatumomab with targeted therapy for BCR-ABL mutant relapsed/refractory acute lymphoblastic leukemia. Leuk Lymphoma 59:2011-2013
Travers, Mark J; Kulak, Jessica A; Vogl, Lisa (2018) Waterpipe cafés are hazardous to your health: Determination of a waterpipe specific calibration factor. Int J Hyg Environ Health 221:48-53
Khoury, Thaer; Nagrale, Vidya; Opyrchal, Mateusz et al. (2018) Prognostic Significance of Stromal Versus Intratumoral Infiltrating Lymphocytes in Different Subtypes of Breast Cancer Treated With Cytotoxic Neoadjuvant Chemotherapy. Appl Immunohistochem Mol Morphol 26:523-532
Yang, Lu; Bhattacharya, Arup; Li, Yun et al. (2018) Anticoagulants inhibit proteolytic clearance of plasma amyloid beta. Oncotarget 9:5614-5626
McManus, Hallie; Moysich, Kirsten B; Tang, Li et al. (2018) Usual Cruciferous Vegetable Consumption and Ovarian Cancer: A Case-Control Study. Nutr Cancer 70:678-683
Welliver, R Ross; Polanco, Jessie J; Seidman, Richard A et al. (2018) Muscarinic receptor M3R signaling prevents efficient remyelination by human and mouse oligodendrocyte progenitor cells. J Neurosci :

Showing the most recent 10 out of 1555 publications