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NCT04880434CompletedPhase 2

Study of Brexucabtagene Autoleucel (KTE-X19) in Participants With Relapsed/Refractory Mantle Cell Lymphoma (Cohort 3)

A Phase 2 Multicenter Study Evaluating the Efficacy of KTE-X19 in Subjects With Relapsed/Refractory Mantle Cell Lymphoma (ZUMA-2)

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

The goal of this clinical study is to test how well the study drug, brexucabtagene autoleucel (KTE-X19), works in participants with relapsed/refractory (r/r) mantle cell lymphoma (MCL) who have not previously received Bruton's tyrosine kinase inhibitor (BTKi).

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
95 (actual)
First submitted
30 Apr 2021
Start date
23 Apr 2021
Primary completion date
17 Jun 2025
Lead sponsor
Kite, A Gilead Company
NCT number
NCT04880434
EudraCT number
2015-005008-27

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 95
  • From 23 Apr 2021 to the primary completion date, 17 Jun 2025
  • 40 sites in 6 countries
  • 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.

Other illness

  • Known history of infection with human immunodeficiency virus (HIV) or hepatitis B (HBsAG positive) or anti-hepatitis C virus (HCV) positive. Individuals with a history of hepatitis infection must have cleared their infection as determined by standard serological and genetic testing
  • History of a seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, cerebral edema, posterior reversible encephalopathy syndrome, or any autoimmune disease with central nervous system (CNS) involvement
  • Presence of fungal, bacterial, viral, or other infection that is uncontrolled or requiring IV antimicrobials for management
    • Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Who the study is looking for

  • Up to 5 prior regimens for mantle cell lymphoma (MCL). Prior therapy must have included anthracycline- or bendamustine-containing chemotherapy and anti-cluster of differentiation 20 (CD20) monoclonal antibody therapy. Individuals must not have received prior therapy with a Bruton's tyrosine kinase inhibitor (BTKi).
  • At least 1 measurable lesion
  • Platelet count ≥ 75,000/μL
  • Creatinine clearance (as estimated by Cockcroft Gault) ≥ to 60 cc/min
  • Cardiac ejection fraction ≥ 50%, no evidence of pericardial effusion as determined by an echocardiogram (ECHO) or multigated acquisition (MUGA), and no clinically significant electrocardiogram (ECG) findings
  • Baseline oxygen saturation \> 92% on room air

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

Full criteria on ClinicalTrials.gov

Sites (40)

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

SiteCityCountrySite status
Johannes Gutenberg University Hospital-University Mainz
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MainzGermanyUnknown status
Munich University of Technology-Medical Faculty- Ethics Committee
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MünchenGermanyUnknown status
Universitaetsklinikum Wuerzburg
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WürzburgGermanyUnknown status
Hospital Clinic Barcelona
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BarcelonaSpainUnknown status
Hospital Universitari Vall d'Hebron
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BarcelonaSpainUnknown status
Hospital Universitario De Salamanca
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SalamancaSpainUnknown status
CHU de Montpellier
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MontpellierFranceUnknown status
Hospital Saint-Louis
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ParisFranceUnknown status
Hopital Haut-Leveque
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PessacFranceUnknown status
Centre Hospitalier Lyon-Sud
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Pierre-BéniteFranceUnknown status
CHU de Rennes
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RennesFranceUnknown status
Queen Elizabeth University Hospital
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GlasgowUnited KingdomUnknown status
Kings College Hospital
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LondonUnited KingdomUnknown status
Manchester Royal Infirmary
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ManchesterUnited KingdomUnknown status
Academisch Medisch Centrum
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AmsterdamNetherlandsUnknown status
University Medical Center Groningen
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GroningenNetherlandsUnknown status
Erasmus MC
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RotterdamNetherlandsUnknown status
Emory University
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AtlantaUnited StatesUnknown status
Dana-Farber Cancer Institute
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BostonUnited StatesUnknown status
University of Chicago
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ChicagoUnited StatesUnknown status
Cleveland Clinic Taussig Cancer Institute
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ClevelandUnited StatesUnknown status
Ohio State University
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ColumbusUnited StatesUnknown status
Baylor Cancer Hospital
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DallasUnited StatesUnknown status
Sarah Cannon- Denver
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DenverUnited StatesUnknown status
Karmanos Cancer Institute
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DetroitUnited StatesUnknown status
Duke University
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DurhamUnited StatesUnknown status
Banner MD Anderson Cancer Center
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GilbertUnited StatesUnknown status
Hackensack University Medical Center
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HackensackUnited StatesUnknown status
MD Anderson Cancer Center
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HoustonUnited StatesUnknown status
Loyola University Medical Center
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MaywoodUnited StatesUnknown status
University of Miami
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MiamiUnited StatesUnknown status
Sarah Cannon - Tenessee
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NashvilleUnited StatesUnknown status
Vanderbilt University
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NashvilleUnited StatesUnknown status
Stanford University
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Palo AltoUnited StatesUnknown status
Advocate Aurora Health - Advocate Lutheran General Hospital
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Park RidgeUnited StatesUnknown status
Fox Chase Cancer Center
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PhiladelphiaUnited StatesUnknown status
University of Rochester
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RochesterUnited StatesUnknown status
University California Los Angeles (UCLA)
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Santa MonicaUnited StatesUnknown status
Swedish Cancer Institute
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SeattleUnited StatesUnknown status
Moffitt Cancer Center
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TampaUnited StatesUnknown status

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