Dasatinib in Relapsed or Refractory Non-Hodgkin's Lymphoma

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

September 17, 2007

Primary Completion Date

August 1, 2016

Study Completion Date

December 1, 2017

Conditions
Non-Hodgkin's Lymphoma
Interventions
DRUG

Dasatinib

"Dasatinib will be orally administered once daily for 28 day cycles.~There will be three dose cohorts for the Dasatinib in the Phase I portion of this trial. A minimum of three patients will be enrolled into each of the following dose cohorts:~Dose cohort # 1 will be 100 mg per day Dose cohort # 2 will be 150 mg per day Dose cohort # 3 will be 200 mg per day~The MTD will be determined in the Phase I portion of this trial."

DRUG

Dasatinib Maximum Tolerated Dose

An additional 29 patients using the Two-Stage Simon design will be enrolled into Phase II using the MTD determined in Phase I.

Trial Locations (1)

68198-7680

University of Nebraska Medical Center, Internal Medicine Section of Oncology/Hematology, Omaha

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

lead

University of Nebraska

OTHER

NCT00550615 - Dasatinib in Relapsed or Refractory Non-Hodgkin's Lymphoma | Biotech Hunter | Biotech Hunter