drugset / Trial / NCT00304200

Temodar and Sutent as Therapy for Melanoma

NCT00304200 ↗

Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study is designed to evaluate the safety and appropriate dose of the combination of Temodar and Sutent as first-line therapy for patients with metastatic malignant melanoma (Phase 1). Once the safety and appropriate dose is determined, additional patients will be studied at that dose to determine if there is clinical benefit as determined by the primary end-point of progression-free survival (PFS) at 6 months and additional secondary endpoints (Phase II).

Timeline

Start
2006-03
Primary completion
2007-10
Completion
2009-01

Outcome

Outcome not reported

Stopped (Business): “Funding was inadequate to continue; Companies requested closure.”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sunitinib Small molecule 25 mg Oral
Subject Temozolomide Small molecule 100 mg/m2 Oral

Indications