drugset / Trial / NCT00150072

Efficacy and Safety of Imatinib in Chordoma

NCT00150072 ↗

Phase 2 Completed 55 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

Preliminary response data, observed by Casali (Cancer, 2004) with imatinib 800 mg/day in patients affected by chordoma, need to be confirmed by a Phase II study, whose primary endpoint will be the formal assessment of clinical and pathological response. Aim of the study will be to explore treatment's activity, but also the potential impact of tumor response, the feasibility and outcome of subsequent surgery and radiotherapy. In addition, patterns of tumour response need to be investigated as well, given the peculiar patterns of response shown with molecular-targeted therapy in solid tumors.

Timeline

Start
2004-10
Primary completion
2008-04
Completion
2008-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Imatinib Small molecule — —

Indications