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
| Type | Name | Description |
|---|---|---|
| DRUG | Rituximab Pfizer | For 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 |
| DRUG | Rituxan | For 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.