Skip to content

All Case Study of Tazemetostat on Safety in Participants

A Study of Tazemetostat on Safety in Participants With Relapsed or Refractory Follicular Lymphoma With Enhancer of Zeste Homolog 2 (EZH2) Gene Mutation in Japan

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT2001220001
Enrollment
145
Registered
2022-04-06
Start date
2021-08-16
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lymphoma, Follicular

Interventions

None listed

Sponsors

Inquiry Service
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Participants with relapsed or refractory follicular lymphoma with EZH2 gene mutation 2. Participants treated with tazemetostat

Exclusion criteria

Exclusion criteria: Participants with a history of hypersensitivity to any ingredient of Tazverik

Design outcomes

Primary

MeasureTime frame
Number of participants with adverse drug reactions and Serious adverse drug reactions.

Secondary

MeasureTime frame
1. Factors considered to affect myelosuppression and infection. 2.Percentage of participants with overall response

Contacts

Public ContactInquiry Service

Eisai Co. Ltd.

eisai-chiken_hotline@hhc.eisai.co.jp+81-120-419-497

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026