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A multi-center and non-interventional registry of Brentuximab Vedotin in patients with relapsed or refractory anaplastic large cell lymphoma or classical Hodgkin lymphoma

Not Applicable
Recruiting
Conditions
Neoplasms
Registration Number
KCT0003789
Lead Sponsor
Samsung Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
150
Inclusion Criteria

1) Any patient planning to administer BrentuximabVedotin to treat the target disease.
2) Any patient administering BrentuximabVedotin to treat the target disease.
3) Any patient tracing BrentuximabVedotin after treating the target disease.
4) Any patient administering another salvage option for cancer as the target disease has relapsed after terminating treatment using BrentuximabVedotin

Exclusion Criteria

If conditions for target diseases are not met.
If conditions for target patients are not met.
If patients do not give written consent to participate in study.

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Overall response rate
Secondary Outcome Measures
NameTimeMethod
Response retention period;Survival with no therapy;Overall survival period;Length of time until next treatment
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