drugset / Trial / NCT00780663

Quarfloxin in Patients With Low to Intermediate Grade Neuroendocrine Carcinoma

NCT00780663 ↗

Phase 2 Completed 25 enrolled Cylene Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a Phase 2, open-label, multicenter, efficacy and safety study of quarfloxin in patients with low or intermediate grade neuroendocrine cancer. The purpose of this study is to evaluate the rate of clinical benefit response to quarfloxin treatment including the reduction in secretory symptoms of flushing and/or diarrhea or the reduction quantifiable hormones or other biochemical tumor markers.

Timeline

Start
2008-10
Primary completion
2010-03
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Quarfloxin Small molecule 240 mg/m2 Intravenous

Indications