drugset / Trial / NCT00310895

Safety and Dose Study of GRN163L Administered to Patients With Refractory or Relapsed Solid Tumor Malignancies

NCT00310895

Phase 1 Completed 85 enrolled Geron Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety and the maximum tolerated dose of GRN163L administration in treating patients with refractory or relapsed solid tumor malignancies.

Timeline

Start
2006-03
Primary completion
2013-03
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Imetelstat Oligonucleotide (other)

Indications

No indication recorded.