Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma
Conditions
Interventions
investigational material(s)
Generic name etc : E7438
INN of investigational material : Tazemetostat
Therapeutic category code : 429 Other antitumor agents
Dosage and Administration for Investigationa
Sponsors
Eisai Co., Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: -Participants with histological diagnosis of B-cell non-Hodgkin's lymphoma (NHL) as follows: --Cohort 1: Follicular lymphoma (FL) --Cohort 2: Diffuse large B-cell lymphoma (including primary mediastinal B-cell lymphoma and transformed FL) -Participants who have confirmed EZH2 gene mutation of tumor in central laboratory -Participants who have measurable disease -Participants who had previous therapy with systemic chemotherapy and/or antibody therapy and for which no standard therapy exists -Participants who had progressive disease or did not have response (complete response or partial response) in previous systemic therapy, or relapsed or progressed after previous systemic therapy -Participants with Eastern Cooperative Oncology Group performance status of 0 to 1 -Participants with life expectancy of >= 3 months from starting study drug administration -Participants with adequate renal, liver, and bone marrow function -Male and female participants >= 20 years of age at the time of informed consent -Participants who has provided written consent to participate in the study
Exclusion criteria
Exclusion criteria: -Participants with prior exposure to EZH2 inhibitor -Participants with a history or a presence of central nerves invasion -Participants with malignant pleural effusion, cardiac effusion, or ascites retention -Participants with allogeneic stem cell transplantation -Participants with medical need for the continued use of potent inhibitors of Cytochrome P450 3A (CYP3A)or potent inducer of CYP3A (including St. John's wort) -Participants with significant cardiovascular impairment -Participants with prolongation of corrected QT interval using Fridericia's formula to > 480 milliseconds (msec) -Participants with venous thrombosis or pulmonary embolism within the last 3 months before starting study drug -Participants with complications of hepatic cirrhosis, interstitial pneumonia or pulmonary fibrosis -Participants with active infection requiring systemic therapy -Women of childbearing potential or man of impregnate potential who don't agree that both the participant and his/her partner will use a medically effective method for contraception for periods from before informed consent to during the clinical study and 30 days later (for males 90 days later) from last administration of study drug
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| safety efficacy Objective response rate (ORR) | — |
Secondary
| Measure | Time frame |
|---|---|
| other - | — |
Countries
Japan
Outcome results
None listed