drugset / Trial / NCT02138955

A Phase IB Dose Escalation Study of Lipocurc in Patients With Cancer

NCT02138955

Phase 1/2 Completed 30 enrolled SignPath Pharma, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a single center in patient/outpatient, uncontrolled dose escalating study in cancer patients to evaluate the safety, tolerability and pharmacokinetic (PK) profiles of body surface area adjusted doses of liposomal curcumin administered intravenously as an 8 hour infusion once weekly for 8 weeks.

Timeline

Start
2014-03
Primary completion
2017-11-30
Completion
2018-02-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Curcumin Small molecule 100 mg/m2 Intravenous
Subject Curcumin Small molecule 300 mg/m2 Intravenous

Indications

No indication recorded.