drugset / Trial / NCT07334574
Clinical Study of XP-006 mRNA Vaccine for R/R B-NHL
Phase 1
Not yet recruiting
20 enrolled
Ruijin Hospital
Shanghai Xinpu BioTechnology Company Limited · collab
NaSingle-groupOpen-labelTreatment
Summary
The main objective of this study is to observe and evaluate the safety and tolerability of the XP-006 personalized tumor mRNA vaccine for the treatment of relapsed or refractory B-cell non-Hodgkin's lymphoma. Secondary objectives focus on evaluating preliminary efficacy through several parameters: XP-006-induced antigen-specific CD4+/CD8+ T cell activation levels, objective remission rate (ORR), complete remission rate (CRR), disease control rate (DCR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS).
Timeline
- Start
- 2026-01-15
- Primary completion
- 2028-01-01
- Completion
- 2029-01-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Personalized neoantigen tumor vaccine | Messenger RNA (mRNA) | 0.2 mg | — |
| Subject | Personalized neoantigen tumor vaccine | Messenger RNA (mRNA) | 0.4 mg | — |
| Subject | Personalized neoantigen tumor vaccine | Messenger RNA (mRNA) | 1 mg | — |