Clinical Trials Directory

Trials / Completed

CompletedNCT06790420

RITUXIMAB BS Intravenous Infusion 100mg・500mg [Pfizer] Post-marketing Database Study

Status
Completed
Phase
Study type
Observational
Enrollment
1 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

To evaluate the incidence of the outcomes for the safety specifications in patients of Medical Data Vision database in Japan diagnosed with CD20 positive B-cell non- Hodgkin's lymphoma who were treated with Rituximab Pfizer to compare it with outcomes in patients who were treated with Rituxan from 01 January 2020 through 31 December 2024

Conditions

Interventions

TypeNameDescription
DRUGRituximab PfizerFor the acute therapy, Rituximab is administrated once a week up to 8 times and for maintenance therapy, it is administrated every 8 weeks up to 12 times
DRUGRituxanFor the acute therapy, Rituximab is administrated once a week up to 8 times and for maintenance therapy, it is administrated every 8 weeks up to 12 times

Timeline

Start date
2025-01-31
Primary completion
2025-03-14
Completion
2025-03-14
First posted
2025-01-24
Last updated
2025-05-31

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT06790420. Inclusion in this directory is not an endorsement.