1
项与 Prostate cancer gene therapy(Biotech Equity Partners) 相关的临床试验A Phase I, Open-label, Dose Escalation Study to Assess the Safety and Tolerability of FP253 in Combination With Fludarabine Phosphate
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.
100 项与 Prostate cancer gene therapy(Biotech Equity Partners) 相关的临床结果
100 项与 Prostate cancer gene therapy(Biotech Equity Partners) 相关的转化医学
100 项与 Prostate cancer gene therapy(Biotech Equity Partners) 相关的专利(医药)
100 项与 Prostate cancer gene therapy(Biotech Equity Partners) 相关的药物交易