For Healthcare Professionals

Tazemetostat for the Treatment of Relapsed/Refractory Follicular Lymphoma

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About the study

Treating Relapsed/Refractory Follicular Lymphoma with Tazemetostat
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

  1. Fully aware this study and signed the informed consent form in voluntary manner, and willing and able to comply with the study procedure;
  2. Age ≥18 years;
  3. Patients with histologically confirmed R/R FL (Grades 1, 2, 3a)
  4. Patients must have one measurable lesion
  5. Life expectancy ≥ 12 weeks;
  6. Eastern Cooperative Oncology Group (ECOG) Performance Status 0 to 2
  7. Adequate bone marrow function, renal function and hepatic function:
  8. Currently human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV) or cytomegalovirus (CMV) is inactive:
  9. Female patients of childbearing potential must agree to adopt dual contraceptive method

EXCLUSION CRITERIA

Exclusion Criteria:

  1. Previous use of Tazemetostat or other EZH2 inhibitors;
  2. Patients with invasion of lymphoma to the central nervous system (CNS) or the pia mater;
  3. Previous bone marrow malignancies,
  4. Abnormalities associated with MDS and myeloproliferative neoplasms observed by cytogenetic testing and DNA sequencing;
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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.
Phone iconCall 19512230542Email iconEmail Study Center

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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