Tazemetostat for the Treatment of Relapsed/Refractory Follicular Lymphoma
About the study
Treating Relapsed/Refractory Follicular Lymphoma with Tazemetostat
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Fully aware this study and signed the informed consent form in voluntary manner, and willing and able to comply with the study procedure;
- Age ≥18 years;
- Patients with histologically confirmed R/R FL (Grades 1, 2, 3a)
- Patients must have one measurable lesion
- Life expectancy ≥ 12 weeks;
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 to 2
- Adequate bone marrow function, renal function and hepatic function:
- Currently human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV) or cytomegalovirus (CMV) is inactive:
- Female patients of childbearing potential must agree to adopt dual contraceptive method
EXCLUSION CRITERIA
Exclusion Criteria:
- Previous use of Tazemetostat or other EZH2 inhibitors;
- Patients with invasion of lymphoma to the central nervous system (CNS) or the pia mater;
- Previous bone marrow malignancies,
- Abnormalities associated with MDS and myeloproliferative neoplasms observed by cytogenetic testing and DNA sequencing;
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study Details
Contition
Relapsed/Refractory Follicular Lymphoma With EZH2
Age
18+
Phase
PHASE2
Participants Needed
39
Est. Completion Date
Feb 29, 2024
Treatment Type
INTERVENTIONAL
Sponsor
Hutchmed
ClinicalTrials.gov NCT Identifier
NCT05467943
Study Number
2021-TAZ-00CH1
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