drugset / Trial / NCT00625430
A Phase I Gene Therapy Study of FP253/Fludarabine for Prostate Cancer
NaSingle-groupOpen-labelTreatment
Summary
The primary objective of this study is to determine the safety and tolerability of a gene-directed enzyme prodrug therapy for prostate cancer. FP253 contains an ovine atadenovirus that expresses the E. coli enzyme purine nucleoside phosphorylase (PNP) under the control of a prostate-directed promoter. PNP converts systemically administered fludarabine (the prodrug) into 2-fluoroadenine (the active agent) at the site where FP253 has been administered (the prostate). This localized conversion is expected to provide organ-targeted chemotherapy that should reduce the systemic side effects associated with classical chemotherapy and also reduce the risk of debilitating damage to tissues surrounding the prostate.
Timeline
- Start
- 2008-03
- Primary completion
- 2012-12
- Completion
- 2012-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | FP253 | Unknown | 1e+09 unknown | Other |
| Subject | FP253 | Unknown | 3.2e+09 unknown | Other |
| Subject | FP253 | Unknown | 1e+10 unknown | Other |
| Subject | FP253 | Unknown | 3.2e+10 unknown | Other |
| Subject | FP253 | Unknown | 1e+11 unknown | Other |
| Subject | FP253 | Unknown | 3.2e+11 unknown | Other |
| Background | Fludarabine | Small molecule | 20 mg/m2 | Intravenous |