drugset / Trial / NCT00441155

Patients Completing Core Protocol (CAMN107A2103), Exhibiting Stable Disease (SD), Partial Response (PR) or Complete Response (CR) to Nilotinib in Combination With Imatinib

NCT00441155 ↗

Phase 1 Completed 14 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To provide study drug to patients that benefit from treatment judged by the investigator - to obtain additional long-term safety and efficacy data of this combination regimen in GIST

Timeline

Start
2006-11
Primary completion
2011-01
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Imatinib Small molecule 0 mg Oral
Subject Imatinib Small molecule 400 mg Oral
Subject Imatinib Small molecule 600 mg Oral
Subject Nilotinib Small molecule 100 mg —
Subject Nilotinib Small molecule 200 mg —
Subject Nilotinib Small molecule 300 mg —
Subject Nilotinib Small molecule 400 mg —