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NCT07819214Not yet recruitingPhase 2

Epcoritamab as Consolidation Therapy for High-Risk Pts w/CLL on BTKI

Epcoritamab as Consolidation Therapy for High-risk Patients With Chronic Lymphocytic Leukemia on Bruton Tyrosine Kinase Inhibitor

Source: ClinicalTrials.gov · Last updated 14 Sept 2026

Brief summary (registry, in English)

This is a phase 2, single-arm, open-label clinical trial determining efficacy of Epcoritamab in subjects with Chronic Lymphocytic Leukemia (CLL) on Burton Tyrosine Kinase Inhibitor (BTKi).

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
24 (estimated)
First submitted
8 Sept 2026
Start date
Oct 2026
Primary completion date
Oct 2028
Lead sponsor
University of California, Irvine
NCT number
NCT07819214

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 24
  • From Oct 2026 to the primary completion date, Oct 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current or prior Richter's transformation

Other illness

  • Second active malignancy requiring treatment (excluding non-melanamatous skin cancers and cancers requiring hormonal therapies alone such as breast/prostate cancer)

Other

  • Active CNS involvement
  • Active immune-mediated cytopenias
  • Pregnant or breastfeeding

Who the study is looking for

  • Patients with CLL and at least 1 of the following risk factors:
    • ≥1 prior line of therapy before BTKi
    • 17p deletion and/or TP53 mutation
    • Complex karyotype (≥3 chromosomal abnormalities)
  • Treated with a BTKi for ≥ 6 months
  • Receiving or able to obtain a commercial supply of BTKi
  • Measurable residual disease defined as the presence of CLL cells by conventional flow cytometry
  • ALC ≤10 K/mcL
  • Lymph nodes ≤5 cm in the longest diameter
  • Normal organ function and hematologic parameters
  • ECOG performance status of 0-1

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chao Family Comprehensive Cancer Center, University of California, Irvine
Coordinator of this site? Confirm its status
OrangeUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.