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

PHASE1CompletedINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

January 31, 2011

Study Completion Date

January 31, 2011

Conditions
Gastrointestinal Stromal Tumors
Interventions
DRUG

Nilotinib, Imatinib

Nilotinib 50 mg and 200 mg gelatin capsules and Imatinib 100 mg and 400 mg film-coated tablets in bottles.. Medication labels for each study drug complied with the legal requirements of each country, were printed in the local language.

Trial Locations (4)

20133

Novartis Investigative Site, Milan

69373

Novartis Investigative Site, Lyon

02115

Dana Farber Cancer Institute, Boston

19111-2497

Fox Chase Cancer Center, Philadelphia

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY