Study of Tisagenlecleucel in Combination With Ibrutinib in r/r Diffuse Large B-cell Lymphoma Patients

Trial ID or NCT#

NCT03876028

Status

not recruiting iconNOT RECRUITING

Purpose

A multi-center, open-label, phase Ib study to evaluate the safety and tolerability of the administration of tisagenlecleucel in combination with ibrutinib in patients with r/r DLBCL who have received two or more lines of systemic therapy, including an anti-CD20 and anthracycline based chemotherapy, and who have progressed after or are not candidates for ASCT.

Official Title

A Phase Ib, Multicenter Study to Determine the Safety and Tolerability of Tisagenlecleucel in Combination With Ibrutinib in Adult Patients With Relapsed and/or Refractory Diffuse Large B-cell Lymphoma

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. 1. Confirmed DLBCL as per the local histopathological assessment. 2. Relapsed or refractory disease having received 2 or more lines of systemic therapy, including anti-CD20 and anthracycline based chemotherapy, and either having progressed after (or relapsed after) ASCT, or being ineligible for or not consenting to ASCT. 3. Measurable disease at time of enrollment. 4. Eastern Cooperative Oncology Group (ECOG) performance status that is either 0 or 1 at screening. 5. Adequate renal, liver, and bone marrow, organ function, and minimum level of pulmonary reserve.
Exclusion Criteria:
  1. 1. Patients with Richter's transformation, Burkitt's lymphoma, and primary DLBCL of the CNS. 2. Prior anti-CD19 directed therapy. 3. Prior gene therapy. 4. Prior adoptive T cell therapy. 5. Prior ibrutinib therapy within the 30 days prior to screening. 6. Patients with active CNS involvement are excluded, except if the CNS involvement has been effectively treated and provided that local treatment was > 4 weeks before enrollment. 7. Prior allogeneic HSCT 8. . Significant cardiac abnormality including history of myocardial infarction within 6 months prior to screening as detailed in the study protocol. Other eligibility criteria may apply.
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Contact

Maria Iglesias
6507234247

View on ClinicalTrials.gov