Clinical trial · Interventional
Study of Recombinant Human-Mouse Chimeric Anti-CD20 Monoclonal Antibody to Treat Non-hodgkin's Lymphoma
An Open-labeled, Multi-center, Randomized, Prospective Phase III Study Comparing CMAB304 in Combination With CHOP to CHOP Alone With CMAB304 Maintenance in Patients With DLBCL
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
CD20, the protein which is expressed on the surface of all mature B cells, is active in many B-cell lymphomas that express this molecule such as Diffuse Large B Cell Lymphoma (DLBCL), the most frequently occurring subtype of non-Hodgkin lymphomas. In clinical practice, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone combination chemotherapy (CHOP) is still considered one of the standard treatment to DLBCL. CMAB304(Retuxira), the chimeric monoclonal antibody is designed to targeted against CD20 for treatment of lymphoma diseases. This trial aimed to observe the safety and efficacy of CMAB304, by added CMAB304 to CHOP chemotherapy regimen compared with CHOP chemotherapy alone.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Diffuse Large B Cell Lymphoma | Diffuse Large B-Cell Lymphoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CHOP, CMAB304 | Drug | — | UNRESOLVED |
| CHOP combined with CMAB304 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- combination group
- interventionNames
- Drug: CHOP combined with CMAB304
- type
- EXPERIMENTAL
- label
- sequential group
- interventionNames
- Drug: CHOP, CMAB304
Primary outcomes (1)
- measure
- overall response rate
- timeFrame
- up to 18 weeks
- description
- Tumor responses were assessed after 6 cycles of CMAB304-CHOP or 6 cycles of CHOP alone and classified as CR,CRu,PR,SD or PD.
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age from 18 to 70 year, male or female 2. Previously untreated 3. DLBCL patients with CD20-positive 4. Lymphoma lesions can be Measured and evaluated; Spiral CT or MR evaluation of the lesion must be ≥ 1cm; Measured by clinical examination or others must be ≥ 2cm 5. Normal blood test, adequate liver and renal function; 6. ECOG score 0\~2 7. Life expectancy of greater than 3 months 8. No other malignancy treatment history, except cured carcinoma in situ of the cervix or squamous cell or basal cell skin cancer 9. Signed ICF Exclusion Criteria: 1. DLBCL transformed from other low-grade NHL types 2. Primary central nervous system lymphoma, or primary gastrointestinal DLBCL 3. History of foreign protein allergies 4. Abnormal liver and/or renal function 5. Suspected or diagnosed central nervous system violation 6. Serious infection or organic diseases 7. Heart disease, heart failure, heart block above second degree, myocardial infarction occurred within six months 8. Breastfeeding or pregnant 9. Leukemia crisis or bone marrow metastases
References
Publications (0)
Data not yet available