RecruitMe Clinical Trial
A Phase 1/2 Multi-Center Study Evaluating the Safety and Efficacy of KTE-X19 in Pediatric and Adolescent Subjects with Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia or Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma (ZUMA-4)
Study Evaluating KTE-C19 in Adolescent Subjects With Acute Lymphoblastic Leukemia or B-Cell Non-Hodgkin Lymphoma (ZUMA-4)
Sponsor: | KITE Pharma |
Enrolling: | Male and Female Patients |
Study Length: | 15 Years |
Clinic Visits: | 40 |
Age Range: | Between 2 and 21 years old |
IRB Number: | AAAS3695 |
U.S. Government ID: | NCT02625480 |
Contact: | Jean Sosna, RN: 212-305-2050 / js4403@cumc.columbia.edu |
Additional Study Information:
The main purpose of this research study is to determine if the experimental product, KTE-C19, when administered after you receive 3 days of chemotherapy, is safe and effective in treating your leukemia or non-Hodgkin lymphoma.
Do You Qualify?
Do you have leukemia or Non-Hodgkin Lymphoma? | Yes | No |
Do you have measurable disease in the Bone Marrow? | Yes | No |
Is CD19 tumor expression on blasts after your most recent completion of therapy? | Yes | No |
Do you have any fungal, bacterial, viral or other infection that is uncontrolled or requiring IV microbials? | Yes | No |
Are you taking corticosteroid therapy at a does of or = to 0.7 mg/kg/day? | Yes | No |