drugset / Trial / NCT01621854

NUC-1031 in Patients With Advanced Solid Tumours

NCT01621854

Phase 1 Completed 68 enrolled Imperial College London Nucana · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a two-part Phase I, open label, dose-escalation, study of NUC-1031 as a single agent in patients with advanced solid tumours who have failed to respond to or who have relapsed after treatment with standard therapy. NUC-1031 is a ProTide of gemcitabine, a drug that has been used widely and effectively against cancers for many years. Both NUC-1031 and gemcitabine work by preventing cancer cells from dividing by attacking their DNA (deoxyribonucleic acid). Non clinical studies have shown that NUC-1031 is more effective than gemcitabine because it is able to reach cancer cells by passive diffusion, is less easily degraded by the cancer cell, and delivers the monophosphate form of the active agent. The first part of the study is to determine recommended phase 2 dose by dose escalation and the second part is to explore preliminary anti-tumour activity.

Timeline

Start
2012-10
Primary completion
2015-06
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject FOSGEMCITABINE PALABENAMIDE Small molecule 500 mg/m2 Intravenous
Subject FOSGEMCITABINE PALABENAMIDE Small molecule 1000 mg/m2 Intravenous
Subject FOSGEMCITABINE PALABENAMIDE Small molecule 2000 mg/m2 Intravenous

Indications