MedPath

Ezharmia Tablet Post-marketing Surveillance

Active, not recruiting
Conditions
Relapsed or refractory Adult T-cell leukemia/lymphoma (ATL)
Registration Number
jRCT2031220503
Lead Sponsor
Daiichi Sankyo Co.,Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Recruiting
Sex
All
Target Recruitment
150
Inclusion Criteria

All patients who start receiving Ezharmia Tablet during the registration period.

Exclusion Criteria

None

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
-

Cumulative incidence of AEs (safety specifications of the survey and other AEs)

Secondary Outcome Measures
NameTimeMethod

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