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Spots Global Cancer Trial Database for Zevalin Post-marketing Surveillance in Japan

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Zevalin Post-marketing Surveillance in Japan

Official Title: Drug Use Investigation of Zevalin

Study ID: NCT01448928

Study Description

Brief Summary: This study is a regulatory post marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Zevalin for relapsed or refractory, CD20+, low grade B-cell non-Hodgkin's lymphoma and Mantle cell lymphoma. The objective of this study is to assess safety and efficacy of using Zevalin in clinical practice. This study is also all case investigation of which the enrollment period is five years, and all patients who received Zevalin will be recruited and followed 13 weeks after the administration.

Detailed Description:

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

, Multiple Locations, , Japan

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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