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Biomarker and diagnostic research for aggressive B-cell non-Hodgkin lymphoma has been reported in the published literature.
8 clinical trials registered, 5 recruiting. Interventions under study include drug therapy, biologic therapy, other interventions, and procedural interventions. Pipeline includes 3 PHASE2, 5 PHASE1. Research is sponsored by a mix of industry and academic institutions.
NCT ID | Title | Phase | Sponsor | Status |
|---|---|---|---|---|
[NCT07097363](https://clinicaltrials.gov/study/NCT07097363) |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:56 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about aggressive B-cell non-Hodgkin lymphoma
Epcoritamab With Dose Adjusted Etoposide, Cyclophosphamide, Vincristine, Doxorubicin, Prednisone and Rituximab (EPOCH-R) for the Treatment of Aggressive B-Cell Non-Hodgkin Lymphoma |
PHASE2 |
University of Washington |
RECRUITING |
[NCT03625037](https://clinicaltrials.gov/study/NCT03625037) | First-in-Human (FIH) Trial in Patients With Relapsed, Progressive or Refractory B-Cell Lymphoma | PHASE1 | Genmab | UNKNOWN |
[NCT06544265](https://clinicaltrials.gov/study/NCT06544265) | SynKIR-310 for Relapsed/Refractory B-NHL | PHASE1 | Verismo Therapeutics | RECRUITING |
[NCT05025800](https://clinicaltrials.gov/study/NCT05025800) | ALX148, Rituximab and Lenalidomide for the Treatment of Indolent and Aggressive B-cell Non-Hodgkin Lymphoma | PHASE1 | M.D. Anderson Cancer Center | ACTIVE_NOT_RECRUITING |
[NCT07432022](https://clinicaltrials.gov/study/NCT07432022) | A Phase I/II Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of the EMB-07 Combination Therapy in Patients With Aggressive B-Cell Non-Hodgkin Lymphoma | PHASE1 | Shanghai EpimAb Biotherapeutics Co., Ltd. | RECRUITING |
63 publications have been identified in PubMed for aggressive B-cell non-Hodgkin lymphoma. Research spans Case Report / Case Series (35%), Review / Meta-Analysis (21%), and Epidemiology / Natural History (16%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 22 | 35% |
Research summaries | 13 | 21% |
Disease patterns and progression | 10 | 16% |
Clinical study results | 8 | 13% |
Laboratory research | 5 | 8% |
New treatment approaches | 3 | 5% |
Testing and diagnosis research | 2 | 3% |
Swomley A (2026). [PMID: 41921675](https://pubmed.ncbi.nlm.nih.gov/41921675/). *Journal of the National Comprehensive Cancer Network : JNCCN*. [Review / Meta-Analysis]
Mao Z (2026). [PMID: 41680140](https://pubmed.ncbi.nlm.nih.gov/41680140/). *Signal transduction and targeted therapy*. [Epidemiology / Natural History]
Gupta T (2026). [PMID: 41585338](https://pubmed.ncbi.nlm.nih.gov/41585338/). *Iranian journal of otorhinolaryngology*. [Case Report / Case Series]
de la Hoz C (2026). [PMID: 41695339](https://pubmed.ncbi.nlm.nih.gov/41695339/). *Frontiers in oncology*. [Diagnostic / Biomarker]
Malik K (2026). [PMID: 41884191](https://pubmed.ncbi.nlm.nih.gov/41884191/). *Clinical medicine insights. Case reports*. [Case Report / Case Series]
Zhang Y (2026). [PMID: 42121877](https://pubmed.ncbi.nlm.nih.gov/42121877/). *Cells*. [Basic Science / Preclinical]
O'Connor E (2026). [PMID: 41297313](https://pubmed.ncbi.nlm.nih.gov/41297313/). *Translational oncology*. [Review / Meta-Analysis]
Li W (2026). [PMID: 41457036](https://pubmed.ncbi.nlm.nih.gov/41457036/). *Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery*. [Review / Meta-Analysis]
Swomley A (2026). [PMID: 42055038](https://pubmed.ncbi.nlm.nih.gov/42055038/). *J Natl Compr Canc Netw*. [Clinical Trial Publication]
Vaughn JL (2026). [PMID: 41510578](https://pubmed.ncbi.nlm.nih.gov/41510578/). *Hematological oncology*. [Epidemiology / Natural History]
AI-curated news mentioning aggressive B-cell non-Hodgkin lymphoma
Updated Feb 13, 2026
A study highlights the curative potential of dual CD19/CD22 CAR-T-cell therapy for patients with TP53-altered relapsed/refractory B-cell non-Hodgkin lymphoma. The findings suggest that combining this therapy with autologous stem cell transplantation may improve long-term outcomes and manage toxicity.