In laboratory cell-line and mouse studies, a Stanford-engineered small molecule that forces two proteins (the lymphoma oncogene BCL6 and the enzyme CDK9) into physical proximity reprogrammed BCL6 to switch ON…
In the single-arm, phase 1/2 EPCORE NHL-1 trial, epcoritamab — a subcutaneously-injected bispecific antibody that physically brings a patient's own T-cells into contact with lymphoma cells — produced an objective…
In the MZL cohort of the single-arm, phase 2 TRANSCEND FL trial, lisocabtagene maraleucel -- a CD19-directed CAR T-cell therapy -- produced an intent-to-treat overall response rate of 84.4% and…
In laboratory cell-line and mouse studies, a Stanford-engineered small molecule that forces two proteins (the lymphoma oncogene BCL6 and the enzyme CDK9) into physical proximity reprogrammed BCL6 to switch ON…
In the single-arm, phase 1/2 EPCORE NHL-1 trial, epcoritamab — a subcutaneously-injected bispecific antibody that physically brings a patient's own T-cells into contact with lymphoma cells — produced an objective…
In the MZL cohort of the single-arm, phase 2 TRANSCEND FL trial, lisocabtagene maraleucel -- a CD19-directed CAR T-cell therapy -- produced an intent-to-treat overall response rate of 84.4% and…
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Last reviewed
Clinical Trials
Important: Eligibility and enrollment are not guaranteed, and listing here is not a treatment recommendation. Talk to your care team.
Laboratory cell-line panels (including 859 distinct cancer cell lines used to test selectivity) and mouse xenograft models of diffuse large B-cell lymphoma (DLBCL) — no human patients have been treated with this compound.
Last reviewed
2026-08-13
Regulatory status by jurisdiction
Unspecified jurisdiction
Status
Investigational
Last verified
2026-08-13
This record has no structured cancer-type scope on file yet — editorial review recommended before treating it as applicable to a specific cancer type.
A Bivalent Molecular Glue Linking Lysine Acetyltransferases to Oncogene-Induced Cell Death (bioRxiv preprint). DOI 10.1101/2025.03.14.643404, PMID 40166243.
Eligibility varies — review trial criteria.
FDA Approvals
Regulatory approval is separate from evidence certainty and from guideline position. Approval applies only to the exact indication stated in each jurisdiction record.
Adults with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) or other large B-cell lymphoma after two or more prior lines of systemic therapy, enrolled in the dose-expansion cohort of the single-arm, open-label, phase 1/2 EPCORE NHL-1 trial.
View approval details
Last reviewed
2026-08-13
Regulatory status by jurisdiction
United States (FDA)
Status
FDA-approved for the exact stated cancer/use
Indication
Adults with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) not otherwise specified (including DLBCL arising from indolent lymphoma) and high-grade B-cell lymphoma, after two or more lines of systemic therapy.
Biomarker requirement
CD20-expressing B-cell lymphoma (target of the bispecific antibody; not a patient-selection biomarker test)
Decision date
2023-05-19
Access notes
Requires a step-up dosing schedule and monitoring for cytokine release syndrome, particularly around the first doses.
Epcoritamab, a Novel, Subcutaneous CD3xCD20 Bispecific T-Cell-Engaging Antibody, in Relapsed or Refractory Large B-Cell Lymphoma: Dose Expansion in a Phase I/II Trial (Journal of Clinical Oncology). DOI 10.1200/JCO.22.01725, PMID 36548927.
Adults with relapsed or refractory marginal zone lymphoma (MZL) who had received at least 2 lines of prior systemic therapy (including an anti-CD20 antibody and an alkylating agent) or who relapsed after stem cell transplantation, enrolled in the MZL cohort of the open-label, single-arm, phase 2 TRANSCEND FL trial.
View approval details
Last reviewed
2026-08-13
Regulatory status by jurisdiction
United States (FDA)
Status
FDA-approved for the exact stated cancer/use
Indication
Adults with relapsed or refractory marginal zone lymphoma who have received at least 2 prior lines of systemic therapy.
Biomarker requirement
CD19-expressing B-cell lymphoma (target of the CAR T-cell construct; not a patient-selection biomarker test)
CancerDiscoveries summarizes verified records in its database. Absence of a listing here does not establish that a treatment lacks regulatory authorization or access.