drugset / Trial / NCT00882180

Dose Escalation Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intravenous ALN-VSP02 In Patients With Advanced Solid Tumors With Liver Involvement

NCT00882180 ↗

Phase 1 Completed 41 enrolled Alnylam Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to determine the safety, tolerability, pharmacokinetics, and pharmacodynamics of intravenous ALN-VSP02, an RNAi therapeutic, in patients with advanced solid tumors with liver involvement.

Timeline

Start
2009-03
Primary completion
2011-07
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject ALN-VSP02 Small interfering RNA (siRNA) — Intravenous

Indications