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CompletedNCT02434484

Symbenda Post-Marketing Surveillance (PMS)

Post-Marketing Surveillance of Symbenda Injection (Bendamustine Hydrochloride) in Korean Patients

Status
Completed
Phase
Study type
Observational
Enrollment
84 (actual)
Sponsor
Eisai Korea Inc. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This is a PMS of Symbenda Injection (bendamustine hydrochloride) in Korean Patients. The main objective is to obtain safety information related to Symbenda treatment from clinical practice.

Conditions

Timeline

Start date
2018-07-04
Primary completion
2020-03-20
Completion
2020-03-20
First posted
2015-05-05
Last updated
2021-01-26

Locations

9 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02434484. Inclusion in this directory is not an endorsement.

Symbenda Post-Marketing Surveillance (PMS) (NCT02434484) · Clinical Trials Directory