Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsPhase2

Zanubrutinib Plus Rituximab for Patients With Indolent Mantle Cell Lymphoma

Sponsor: University College, London

NCT ID: NCT05635162

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Zanubrutinib (drug), Rituximab (drug)
How long the study runs
Study runs about 53 months (dates as stated)
About the drug or intervention
Zanubrutinib — drug: Zanubrutinib dose is 160 mg twice daily (BD) orally (PO) on days 1-28 of each 28-day cycle. · Rituximab — drug: Rituximab 375 mg/m2 intravenous (IV)\* on day 1 (+/-3 days) of each 28-day cycle
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
50
Started
2024-05-17
Last checked
2025-04

Plain English Summary

What is this study?

  • • Testing a new treatment for mantle cell lymphoma
  • • Phase2 - 50 participants
  • • Phase II, multicentre, randomised, open-label study to assess the benefit of early intervention with fixed duration, time-limited zanubrutinib-rituximab in indolent mantle cell lymphoma (MCL)

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with mantle cell lymphoma

Where?

  • • Derby - Royal Derby Hospital
  • • Glasgow - Beatson West of Scotland Cancer Centre
  • • Liverpool - Clatterbridge Cancer Centre
  • • London - Guy's Hospital
  • • +9 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Phase II, multicentre, randomised, open-label study to assess the benefit of early intervention with fixed duration, time-limited zanubrutinib-rituximab in indolent mantle cell lymphoma (MCL)

More detail

This is a phase II, multicentre, randomised open label study to assess the safety and efficacy of zanubrutinib in combination with rituximab for previously untreated indolent MCL patients. 50 patients will be recruited from 15 UK centres over 30 months. Enrolled patients will be randomised (1:1) to ongoing observation (control arm; arm A) or fixed-duration zanubrutinib-rituximab (experimental arm; arm B). Patients will discontinue zanubrutinib-rituximab after 6 cycles of therapy or sooner in the advent of unacceptable toxicity or any other reason. All patients will be followed up for a minimum of 2 years after randomisation. Patients in arm B who develop disease progression and require further therapy after the initial time-limited Zanu-R will receive standard of care therapy according to front line treatment available at that time.

Mantle Cell Lymphoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Biomarkers mentioned

have a negativeHbsAg positivePCR positiveantibody positivePCR negative

Treatment history

Treatments you must have had:

  • ✓ evaluations and procedures in this study protocol including swallowing capsules without difficulty

What the study is looking for

  • ✓18 years of age or over.
  • ✓Life expectancy ≥ 6 months.
  • ✓Pathologically confirmed MCL, with documentation of monoclonal B cells that have a chromosome translocation...
  • ✓Stage II-IV MCL measurable by CT imaging or by white cell count (WCC)/BM infiltration.
  • ✓'Indolent' MCL, defined as 1 or more of the following:

Who cannot take part

  • ✗Any prior therapy for MCL, including prior radiotherapy.
  • ✗Central nervous system (CNS) involvement of MCL.
  • ✗No progression requiring treatment since initial diagnosis.
  • ✗Vaccinated with live vaccines (not including messenger ribonucleic acid (mRNA), viral vector or other non-live...
  • ✗Requirement for moderate or strong CYP3A inducers. Moderate and strong CYP3A inhibitors are allowed although these...
See the full criteria
Inclusion Criteria: 1. 18 years of age or over. 2. Life expectancy ≥ 6 months. 3. Pathologically confirmed MCL, with documentation of monoclonal B cells that have a chromosome translocation t(11;14)(q13;q32) and/or overexpress cyclin D1, D2 or D3. 4. Stage II-IV MCL measurable by CT imaging or by white cell count (WCC)/BM infiltration. 5. 'Indolent' MCL, defined as 1 or more of the following: * Observation with no treatment for a minimum of 6 months after the initial diagnosis * Leukaemic non-nodal variant (lymphocytosis/splenomegaly only without nodal involvement) * Low tumour volume (largest lymph node ≤ 3cm in maximal diameter), proliferation fraction (Ki67 or equivalent) ≤30% and classical morphology (non-blastoid/pleomorphic) 6. Eastern Cooperative Oncology Group (ECOG) Performance Status 0-2. 7. Absolute neutrophil count ≥1.0 x 109/L and platelets ≥75 x 109/L independent of growth factor support. 8. AST and/or ALT ≤3 x upper limit of normal (ULN). 9. Total Bilirubin ≤1.5 x ULN unless due to Gilberts syndrome or of non-hepatic origin unless directly attributable to the patient's MCL. 10. Calculated creatinine clearance ≥30 mL/min. Glomerular filtration rate (GFR) ≥30 mL/min directly measured with 24 hour urine collection, or creatinine clearance calculated according to the modified formula of Cockcroft and Gault (for men: GFR ≈ ((140 - age) x bodyweight)/ (72 x creatinine), for women x 0, 85). 11. Able to give voluntary written informed consent. 12. Willing and able to participate in all required evaluations and procedures in this study protocol including swallowing capsules without difficulty. 13. Negative serum or urine pregnancy test for women of childbearing potential (WOCBP). 14. Willing to comply with the contraceptive requirements of the trial. Exclusion Criteria: 1. Any prior therapy for MCL, including prior radiotherapy. 2. Central nervous system (CNS) involvement of MCL. 3. Uncontrolled infection with HIV or any uncontrolled active systemic infection (e.g., bacterial, viral or fungal). Patients with well-controlled HIV status (undetectable viral load) will not be excluded. 4. Hepatitis B or C serologic status: subjects who are hepatitis B core antibody (anti-HB core) positive and who are surface antigen (HBsAg) negative will need to have a negative polymerase chain reaction (PCR) test. Those who are hepatitis B HbsAg positive or hepatitis B PCR positive will be excluded. Those who are hepatitis C antibody and PCR positive will be excluded (those who are hepatitis C antibody positive and PCR negative will not be excluded). 5. No progression requiring treatment since initial diagnosis. 6. Vaccinated with live vaccines (not including messenger ribonucleic acid (mRNA), viral vector or other non-live COVID19 vaccines) within four weeks prior to randomisation. 7. Major surgical procedure within 28 days prior to randomisation. Note: If a subject had major surgery, they must have recovered adequately from any toxicity and/or complications from the intervention before the first dose of study drug. 8. Prior malignancy (or any other malignancy requiring active treatment), except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, localised prostate cancer or other cancer from which the subject has been disease free for ≥ 2 years or which will not limit survival to \< 5 years. 9. Requirement for moderate or strong CYP3A inducers. Moderate and strong CYP3A inhibitors are allowed although these should be switched to agents causing less CYP3A inhibition where possible. 10. Requirement for vitamin K antagonists (alternative anticoagulation is allowed (e.g. DOACs), but patients must be properly informed about the potential risk of bleeding alongside zanubrutinib). Requires ongoing treatment with warfarin or warfarin derivatives 11. Active bleeding or history of bleeding diathesis (e.g. haemophilia or von Willebrand disease) or history of spontaneous bleeding requiring blood transfusion or other medical intervention. 12. Clinically significant cardiovascular disease such as uncontrolled arrhythmias, or history of ventricular tachycardia, ventricular fibrillation, torsades de points or myocardial infarction within 6 months of randomisation, or any Class 3 or 4 cardiac disease as defined by the New York Heart Association (NYHA) Functional Classification, or corrected QT interval (QTc) \> 480 msec, second-degree atrioventricular block Type II, third-degree atrioventricular block at randomisation, unstable angina within 3 months prior to randomisation. 13. History of stroke or intracranial haemorrhage within 6 months prior to randomisation. 14. Any other severe medical or psychiatric illness that in the opinion of the investigator would interfere with participation in this clinical study. 15. Malabsorption syndrome, unable to swallow capsules, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel that is likely to affect absorption, symptomatic inflammatory bowel disease, partial or complete bowel obstruction, or gastric restrictions and bariatric surgery, such as gastric bypass. 16. Women who are pregnant or breastfeeding. 17. Male participants with female partners of childbearing potential who are unwilling to use appropriate contraception methods. 18. Concurrent treatment with another investigational agent. 19. History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies, known sensitivity or allergy to murine products. 20. Known hypersensitivity to any active substance or to any of the excipients of one of the drugs used in the trial. 21. Severe or debilitating pulmonary disease. 22. Underlying medical conditions that, in the investigator's opinion, will render the administration of study drug hazardous or obscure the interpretation of toxicity or AEs 23. Concurrent participation in another therapeutic clinical trial. 24. Active and/or ongoing autoimmune anaemia and/or autoimmune thrombocytopenia (eg. idiopathic thrombocytopenia purpura).

Where Is This Study? (13 UK sites)

Royal Derby Hospital

Derby, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Teresa Grieve

uhdb.researchgov@nhs.net01332 724639 / 01332 724638

Beatson West of Scotland Cancer Centre

Glasgow, United Kingdom

Recruiting
Hospital R&D contact (matched)

Jennifer McLean

jennifer.mclean@health.scot.nhs.uk0131 537 4718

Clatterbridge Cancer Centre

Liverpool, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Maria Maguire

maria.maguire2@nhs.net0151 556 5321

Guy's Hospital

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Main Email: gstt.research.rbhh@nhs.net

gstt.research.rbhh@nhs.netn/a

St Bartholomew's Hospital

London, United Kingdom

Recruiting

University College London Hospital

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Rajinder Sidhu - Associate Director, Research Governance and Operations

uclh.jro-communications@nhs.net020 3447 9825

Christie Hospital

Manchester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Innovation Office

the-christie.ri@nhs.net---

Norfolk and Norwich University Hospitl

Norwich, United Kingdom

Recruiting
Hospital R&D contact (matched)

Julie Dawson

rdsubmissions@nnuh.nhs.uk01603 286611

Nottingham City Hospital

Nottingham, United Kingdom

Recruiting
Hospital R&D contact (matched)

Alison Lloyd

nuhnt.researchsponsor@nhs.net0115 9249924

Churchill Hospital

Oxford, United Kingdom

Recruiting

Derriford Hospital

Plymouth, United Kingdom

Recruiting

Southampton General Hospital

Southampton, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Mikayala King

researchmanagement@uhs.nhs.uk023 81208215

Royal Cornwall Hospital

Truro, United Kingdom

Recruiting
Hospital R&D contact (matched)

Abi Weeks

rch-tr.CornwallResearch@nhs.net01872 25 6424

How to Get in Touch

ZEBRA Trial Manager

Sponsor contact

CONTACT

(+44) (0)2076799860 ctc.zebra@ucl.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2025-04