A Multicenter, Retrospective Observational Study to Evaluate the Effectiveness and Safety of Polatuzumab Vedotin
- Sponsor
- Jiangsu Cancer Institute & Hospital
- Study ID
- NCT04624893
- Status
- Unknown
Conditions
- Diffuse Large B-Cell Lymphoma (DLBCL)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Polatuzumab Vedotin-Piiq — DRUGPatients will receive a total of six cycles of Pola in combination with rituximab and bendamustine or in combination with only rituximab. A cycle is typically 21 days for DLBCL.
Study Details
To assess the clinical outcomes following treatment with Pola in combination with Bendamustine, Rituximab (BR) or Rituximab (R) in patients with R/R DLBCL who are not eligible for transplantation in the real-world setting.
Key Dates
- Start date
- Dec 12, 2019
- Status verified
- Nov 2020
- Primary completion
- Dec 31, 2020
- Completion
- Dec 31, 2020
Study Design
- Enrollment
- 35 participants (estimated)
Arms
- Arm: Pola BR/RPatients with R/R DLBCL who are enrolled in the Pola CUP program in China, and treated with Pola-BR or Pola-R regimens.
Primary Outcome Measure
Investigator-assessed best overall response (BOR) [ Time Frame: From the start of the treatment until the date of first documented progression or the completion of the treatment(up to six cycles, each cycle is 21 days) ]
Central Contacts
- Jianqiu Wu, Ph.D+86-13951671579
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