drugset / Trial / NCT00625430

A Phase I Gene Therapy Study of FP253/Fludarabine for Prostate Cancer

NCT00625430 ↗

Phase 1 Unknown 18 enrolled Biotech Equity Partners Pty Ltd
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

EvaluationDrugModalityDoseRoute
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

Indications