The first Gene Therapy clinical trials begin at the Johns Hopkins University in 1992. Material for these studies was generated in part by a small Good Laboratory Practice (GLP) facility on the third floor of the Ross Building and in part by an outside GMP facility. The small GLP facility has since been replaced by The Johns Hopkins University Cell Processing and Gene Therapy Laboratories. These laboratories are composed of two administratively linked laboratories: a 400 square foot GLP room (the Developmental Immunology Laboratory) for pre-scale up development and for scale-up of therapies that can be performed with minimal manipulation and/or in a closed system; and an 1800 square foot fully cGMP facility for the manufacture of clinical grade, bio-therapeutic material for gene therapy phase I and II clinical studies. Five to seven individuals with training in cGMP, cellular and viral manipulations, as well as process development staff the Core facility. The configuration of the Cell Processing and Gene Therapy Facilities allows the simultaneous processing of four clinical products, with development of two to three pre-clinical scale-up projects within the Development Laboratory. This Core is currently utilized by more than ten faculty members who represent five programs within the Oncology department, and faculty members from at least two other departments in the School of Medicine. The mission of the Cell Processing and Gene Therapy Facility at Johns Hopkins University is to act as a resource within the Johns Hopkins Community, providing expertise for the advancement of basic research on human somatic cell and gene therapy. Specifically, this facility supports translational research with: 1) in-house cell expansion and cell separation expertise for phase I and II clinical trials; 2) in-house manufacturing of clinical grade, bio-therapeutics for phase I and II clinical trials; and 3) production of biologic agents under current Good Manufacturing Practices (cGMP) as advised by the United States Food and Drug Administration to ensure the safest possible products for our patients. This CORE facility has already accelerated the initial clinical testing of several vaccines that were developed in laboratories at the Johns Hopkins University. Because the translational activity in somatic cell and gene therapy within the Cancer Center is quite substantial, we expect this CORE to continue to facilitate the clinical development of new therapies for most types of cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA006973-39
Application #
6481453
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
1978-01-01
Project End
2006-04-30
Budget Start
Budget End
Support Year
39
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Kaur, Harsimar B; Guedes, Liana B; Lu, Jiayun et al. (2018) Association of tumor-infiltrating T-cell density with molecular subtype, racial ancestry and clinical outcomes in prostate cancer. Mod Pathol 31:1539-1552
Connolly, Roisin M; Fackler, Mary Jo; Zhang, Zhe et al. (2018) Tumor and serum DNA methylation in women receiving preoperative chemotherapy with or without vorinostat in TBCRC008. Breast Cancer Res Treat 167:107-116
Ye, I Chae; Fertig, Elana J; DiGiacomo, Josh W et al. (2018) Molecular Portrait of Hypoxia in Breast Cancer: A Prognostic Signature and Novel HIF-Regulated Genes. Mol Cancer Res 16:1889-1901
Zhu, Yezi; Sharp, Adam; Anderson, Courtney M et al. (2018) Novel Junction-specific and Quantifiable In Situ Detection of AR-V7 and its Clinical Correlates in Metastatic Castration-resistant Prostate Cancer. Eur Urol 73:727-735
Lu, Yunqi; Hu, Zhongyi; Mangala, Lingegowda S et al. (2018) MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels. Cancer Res 78:64-74
Rao, Karthik; Liang, Stella; Cardamone, Michael et al. (2018) Cost implications of PSA screening differ by age. BMC Urol 18:38
Johnson, Renee M; Fleming, Charles B; Cambron, Christopher et al. (2018) Race/Ethnicity Differences in Trends of Marijuana, Cigarette, and Alcohol Use Among 8th, 10th, and 12th Graders in Washington State, 2004-2016. Prev Sci :
Marrone, Kristen A; Zhou, Xian; Forde, Patrick M et al. (2018) A Randomized Phase II Study of Metformin plus Paclitaxel/Carboplatin/Bevacizumab in Patients with Chemotherapy-Naïve Advanced or Metastatic Nonsquamous Non-Small Cell Lung Cancer. Oncologist 23:859-865
Bar-Shir, Amnon; Alon, Lina; Korrer, Michael J et al. (2018) Quantification and tracking of genetically engineered dendritic cells for studying immunotherapy. Magn Reson Med 79:1010-1019
Altekruse, Sean F; Shiels, Meredith S; Modur, Sharada P et al. (2018) Cancer burden attributable to cigarette smoking among HIV-infected people in North America. AIDS 32:513-521

Showing the most recent 10 out of 2393 publications