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NCT06242834

Pembrolizumab and Tazemetostat to Overcome Immune Tolerance Following ASCT or CAR T-cell Therapy in Patients With Aggressive B-Cell Non-Hodgkin's Lymphoma

Active, enrolled Phase 2 Last updated 1 April 2026
What this trial tests

Phase 2 trial testing Biospecimen Collection in B-Cell Non-Hodgkin Lymphoma in 32 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
30 September 2024
Primary endpoint
24 April 2027
24 November 2028

Quick facts

Lead sponsorNorthwestern University
PhasePhase 2
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment32
Start date30 September 2024
Primary completion24 April 2027
Estimated completion24 November 2028
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Northwestern University

Who can join

18 and older, any sex, with B-Cell Non-Hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This phase II trial tests how well pembrolizumab and tazemetostat work to treat patients who have received autologous stem cell transplantation (ASCT) or chimeric antigen receptor (CAR) T cell therapy for aggressive non hodgkins lymphoma. A monoclonal antibody, such as pembrolizumab, is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Tazemetostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving pembrolizumab and tazemetostat may work better to treat patients who have received ASCT or CAR-T cell therapy for aggressive non hodgkins lymphoma.

Publications & conference data

5 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Epigenetic drugs in cancer therapy.
    Suraweera A, O'Byrne KJ, Richard DJ. · · 2025 · cited 50× · PMID 40011240 · DOI 10.1007/s10555-025-10253-7
  2. Mechanisms of Resistance to CAR T-Cells and How to Overcome Them.
    Legato L, Bisio M, Fasano F, Benevolo Savelli C, et al · · 2025 · cited 3× · PMID 40981226 · DOI 10.3390/mps8050108
  3. Genomic and Immune Correlates of EZH2 Expression and Activity in Olfactory Neuroblastoma.
    Xue E, Adeyelu T, Krause H, Elliott A, et al · · 2026 · cited 1× · PMID 41221671 · DOI 10.1002/hed.70076
  4. The role of <i>EZH2</i> dysregulation in the pathogenesis of B-cell lymphomas and its implications as a target therapy.
    Candelaria M. · · 2026 · PMID 42211521 · DOI 10.3389/fonc.2026.1843273
  5. Targeting epigenetic regulators to boost T cell immunotherapy against cancer.
    Xiao T, Zhang YE. · · 2026 · PMID 41634788 · DOI 10.1186/s13578-026-01533-y

Verify or expand the search:

Other trials of Biospecimen Collection

Trials testing the same drug.

Other recruiting trials for B-Cell Non-Hodgkin Lymphoma

Currently open trials in the same condition.

Other Northwestern University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06242834.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing