Acute Myeloid Leukemia Clinical Trial
A Safety Study of SGN-CD19A for Leukemia and Lymphoma
Summary
This is a phase 1, open-label, dose-escalation, multicenter study to evaluate the safety and tolerability of SGN-CD19A in adult and pediatric patients with relapsed or refractory B-lineage acute lymphoblastic leukemia (B-ALL), Burkitt lymphoma or leukemia, or B-lineage lymphoblastic lymphoma (B-LBL).
Eligibility Criteria
Inclusion Criteria:
Adult patients must be relapsed or refractory to at least 1 prior multi-agent systemic therapy. Pediatric patients must be relapsed or refractory to at least 2 prior multi-agent systemic therapies. Patients with acute lymphoblastic leukemia who are Philadelphia chromosome-positive must have failed a second generation tyrosine kinase inhibitor.
Eastern Cooperative Oncology Group status of 2 or lower
Pathologically confirmed diagnosis of B-lineage acute lymphoblastic leukemia, Burkitt leukemia or lymphoma, or B-lineage lymphoblastic lymphoma
Measurable disease
Exclusion Criteria:
Allogeneic stem cell transplant within 60 days, active acute or chronic graft-versus-host disease (GvHD), or receiving immunosuppressive therapy as treatment for GvHD
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There are 12 Locations for this study
Birmingham Alabama, 35233, United States
Birmingham Alabama, 35294, United States
Scottsdale Arizona, 85259, United States
Duarte California, 91010, United States
Jacksonville Florida, 32224, United States
Saint Petersburg Florida, 33701, United States
Tampa Florida, 33612, United States
Atlanta Georgia, 30322, United States
Boston Massachusetts, 02114, United States
Boston Massachusetts, 02215, United States
Boston Massachusetts, 02215, United States
New York New York, 10021, United States
Cincinnati Ohio, 45229, United States
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