Axicabtagene Ciloleucel for Consolidation After First-line Treatment of High-risk Large B-cell Lymphoma
Condition(s) studied
Investigational drug(s) / intervention(s)
Axicabtagene Ciloleucel: Axicabtagene Ciloleucel at 2.0×10\^6/Kg
Study summary
The goal of this clinical trial is to learn if Axicabtagene Ciloleucel (axi-cel) works for consolidation after first-line treatment of high-risk Large B-cell Lymphoma (LBCL). It will also learn about the safety of axi-cel treatment. The main questions it aims to answer are:
* Does axi-cel treatment result in prolonged clinical benefit to patients with high-risk LBCL after first-line treatment?
* What medical problems do participants have when receiving axi-cel treatment?
In this investigator-initiated, single-arm clinical trial, participants will:
* Receive atezolizumab treatment at 2.0×10\^6 cells/Kg as a one-time therapy.
* Visit the clinic as instructed for checkups and tests.
Eligibility
Primary outcome measure(s)
- one year PFS — From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| The First Affiliated Hospital of Zhengzhou University, Department of Oncology | Zhengzhou | Henan | Recruiting |
On this site
📄 Yescarta (axicabtagene ciloleucel) drug profile →More Zhengzhou University trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06609304 on ClinicalTrials.gov ↗ ← All trials in China