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Looking for participantsPhase2/Phase3

Rituximab and Ibrutinib (RI) Versus Dexamethasone, Rituximab and Cyclophosphamide (DRC) as Initial Therapy for Waldenström's Macroglobulinaemia

Sponsor: University College, London

NCT ID: NCT04061512

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
Dexamethasone, cyclophosphamide, rituximab (drug), Rituximab, ibrutinib (drug)
How long the study runs
Study runs about 121 months (dates as stated)
About the drug or intervention
Dexamethasone, cyclophosphamide, rituximab — drug: DRC Arm (chemotherapy) consists of dexamethasone, cyclophosphamide and rituximab treatment · Rituximab, ibrutinib — drug: RI Arm (chemotherapy free) consists of rituximab and ibrutinib treatment
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
148
Started
2020-02-03
Last checked
2024-05

Plain English Summary

What is this study?

  • • Testing a new treatment for waldenstrom macroglobulinemia
  • • Phase2/Phase3 - 148 participants
  • • Waldenström's macroglobulinaemia (WM) is a rare type of slow growing lymphoma

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with waldenstrom macroglobulinemia

Where?

  • • Bath - Royal United Hospital, Bath
  • • Bournemouth - The Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust
  • • Canterbury - East Kent Hospitals University NHS Foundation Trust
  • • Cardiff - University Hospital of Wales
  • • +21 more UK sites

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

About This Trial

Waldenström's macroglobulinaemia (WM) is a rare type of slow growing lymphoma. It develops when white blood cells grow abnormally. Typically a disease of the elderly, the median age of presentation is \>70 years and the current treatment for WM is unsatisfactory, with incomplete responses and inevitable recurrence. Therefore there is a need to find alternative treatments that are more effective, leading to lasting responses and improved quality of life. The RAINBOW study is a phase 2-3 trial assessing 'chemotherapy free' treatment as primary therapy for WM which can potentially improve response outcome, durability and importantly, reduce toxicity for WM patients. This approach will be done using the drug Ibrutinib, which in combination with rituximab (RI) will be the experimental arm. As there is no agreed standard on first-line therapy for WM, the control arm is the current treatment based on the most recently published clinical trial results. The control arm consists of rituximab, cyclophosphamide and dexamethasone (DCR), and is widely recommended by international consensus as appropriate treatment for first-line therapy for WM. In this study, 148 adults (aged ≥ 18 years) with treatment naïve WM will be randomised on a 1:1 ratio to either the treatment or control arm. Randomised treatment lasts for a maximum of 6 cycles and response will be assessed following 3 cycles of treatment and completion of randomised treatment at approximately 24 weeks after commencing treatment. RI patients may then have up to 5 years of Ibrutinib monotherapy. Patients will be seen regularly during treatment and then every 3 months for 5 years after treatment discontinuation. Patients will enter annual follow up for survival until the end of trial (including progressed patients). The study will be conducted at NHS hospitals and is expected to last 9 years and 6 months.

Waldenstrom Macroglobulinemia

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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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

if negativeHBcAb positiveand if positive

What the study is looking for

  • ✓Patients ≥ 18 years
  • ✓Confirmed diagnosis of WM (according to consensus panel / WHO criteria) with measurable IgM paraprotein
  • ✓Previously untreated disease at any stage requiring therapy at the discretion of the treating physician. Suggested...
  • ✓haematological suppression to Hb \<10g/dl, or neutrophils \<1.5x109/l or platelets \<150x109/l
  • ✓clinical evidence of hyperviscosity

Who cannot take part

  • ✗Prior therapy for WM
  • ✗Lymphoplasmacytic lymphoma with no detectable serum IgM paraprotein
  • ✗CNS involvement with WM
  • ✗Autoimmune cytopenias
  • ✗Major surgery within 4 weeks prior to randomisation
See the full criteria
Inclusion Criteria: 1. Patients ≥ 18 years 2. Confirmed diagnosis of WM (according to consensus panel / WHO criteria) with measurable IgM paraprotein 3. Previously untreated disease at any stage requiring therapy at the discretion of the treating physician. Suggested criteria for initiating treatment include: * haematological suppression to Hb \<10g/dl, or neutrophils \<1.5x109/l or platelets \<150x109/l * clinical evidence of hyperviscosity * bulky lymphadenopathy and/or bulky splenomegaly * presence of B symptoms 4. No previous chemotherapy (prior plasma exchange and steroids are permissible) 5. Eastern Cooperative Oncology Group (ECOG) performance status grade 0 - 2 6. Life expectancy of greater than 6 months 7. Written informed consent 8. Willing to comply with the contraceptive requirements of the trial 9. Negative serum or urine pregnancy test for women of childbearing potential (WOCBP) Exclusion Criteria: 1. Prior therapy for WM 2. Lymphoplasmacytic lymphoma with no detectable serum IgM paraprotein 3. CNS involvement with WM 4. Autoimmune cytopenias 5. Major surgery within 4 weeks prior to randomisation 6. Clinically significant cardiac disease including the following: * Myocardial infarction within 6 months prior to randomisation * Unstable angina within 3 months prior to randomisation * New York Heart Association class III or IV congestive heart failure * History of clinically significant arrhythmias (e.g. sustained ventricular tachycardia, ventricular fibrillation, torsades de pointes) * QTcF \> 480 msecs based on Fredericia's formula or Bazette's formula * History of Mobitz II second degree or third degree heart block without a permanent pacemaker in place * Uncontrolled hypertension as indicated by a minimum of 2 consecutive blood pressure measurements showing systolic blood pressure \> 170 mmHg and diastolic blood pressure \> 105 mm Hg * Cardiac event within 6 months of screening (e.g. coronary artery stent) requiring dual antiplatelet treatment 7. History of stroke or intracranial haemorrhage within 6 months prior to randomisation 8. Requires anticoagulation with warfarin or equivalent vitamin K antagonists (direct oral anticoagulants (DOACs) allowed) 9. History of severe bleeding disorders considered not to be disease related (Haemophilia A, B or von Willebrand's disease) 10. Requires ongoing treatment with a strong CYP3A inhibitor or inducer 11. Known infection with HIV, or serologic status reflecting active hepatitis B or C infection as follows: * Presence of hepatitis B surface antigen (HBsAg). In addition, if negative for HBsAg but HBcAb positive (regardless of HBsAb status), a HB DNA test will be performed and if positive the patient will be excluded * Presence of hepatitis C virus (HCV) antibody. Patients with presence of HCV antibody are eligible if HCV RNA is undetectable 12. Women who are pregnant or breastfeeding or males expecting to conceive or father children at any point from the start of treatment until the end of the "at risk period" 13. Renal failure (creatinine clearance \<30 ml/min as estimated by the Cockroft-Gault equation) 14. Patients with chronic liver disease with hepatic impairment Child-Pugh class B or C 15. Known history of anaphylaxis following exposure to rat or mouse derived CDR-grafted humanised monoclonal antibodies. 16. Inability to swallow oral medication 17. Disease significantly affecting gastrointestinal function and/or inhibiting small intestine absorption (e.g. malabsorption syndrome, resection of the small bowel, poorly controlled inflammatory bowel disease) 18. Active systemic infection requiring treatment 19. Concomitant treatment with another investigational agent 20. Any life-threatening illness, medical condition, organ system dysfunction, need for profound anticoagulation, or bleeding disorder, which, in the investigator's opinion, could compromise the patient's safety, or put the study at risk 21. Unwilling or unable to take PCP prophylaxis (e.g. cotrimoxazole) 22. History of prior malignancy, with the exception of the following: * Malignancy treated with curative intent and with no evidence of active disease present for more than 3 years prior to screening and felt to be at low risk for recurrence by treating physician * Adequately treated non-melanomatous skin cancer or lentigo maligna melanoma, superficial bladder cancer, carcinoma in situ of the cervix or breast or localized Gleason score 6 prostate cancer without current evidence of disease.

Where Is This Study? (25 UK sites)

Royal United Hospital, Bath

Bath, United Kingdom

Recruiting
Hospital R&D contact (matched)

Amy Lloyd

ruh-tr.researchgovernance@nhs.net01225 821669

The Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust

Bournemouth, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research Development & Support

clinicalresearch@bournemouth.ac.uk01202 961200

East Kent Hospitals University NHS Foundation Trust

Canterbury, United Kingdom

Recruiting
Hospital R&D contact (matched)

Caroline Cowley, Research & Innovation/Clinical Trials Unit Manager

ekhuft.researchandinnovation@nhs.net01227 783169

University Hospital of Wales

Cardiff, United Kingdom

Recruiting
Hospital R&D contact (matched)

Elen de Lacy

PHW.Research@wales.nhs.uk02920 104468

Colchester Hospital

Colchester, United Kingdom

Recruiting

Mid Yorkshire NHS Trust

Dewsbury, United Kingdom

Recruiting
Hospital R&D contact (matched)

Judith Holliday

Midyorks.My.Research@nhs.net01924 543772

Royal Devon University Hospital

Exeter, United Kingdom

Recruiting
Hospital R&D contact (matched)

Samantha Smart

rduh.research-eastern@nhs.net01392 406075

Medway Maritime Hospital

Gillingham, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Jennifer Teke

j.teke@nhs.net01634 976918

Castle Hill Hospital

Hull, United Kingdom

Recruiting
Hospital R&D contact (matched)

James Illingworth

hyp-tr.development.research@nhs.net01482 461883 or 461903

NHS Lanarkshire

Lanark, United Kingdom

Recruiting
Site contact (verified)
Iain SingerPrincipal Investigator

St James's University Hospital

Leeds, United Kingdom

Recruiting
Hospital R&D contact (matched)

R&I Team

leedsth-tr.researchfacilitation@nhs.net0113 2060469

Leicester Royal Infirmary

Leicester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Carolyn Maloney

uhl-tr.researchandinnovationadminmailbox@nhs.net0116 258 8351

Barking, Havering and Redbridge University Hospitals NHS Trust

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Heidi Chandler

bhrut.development.research@nhs.net01708 435000 ex 2923

Barts Health NHS Trust

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Mays Jawad

research.governance@qmul.ac.uk020 7882 6826

King's College Hospital

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Jasmine Palmer

kch-tr.research@nhs.net0203 299 1980

Northwick Park Hospital

London, United Kingdom

Recruiting

University College London Hospitals NHS Foundation Trust

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 NHS Foundation Trust

Manchester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Innovation Office

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

Norfolk and Norwich Hospital

Norwich, United Kingdom

Recruiting
Hospital R&D contact (matched)

Julie Dawson

rdsubmissions@nnuh.nhs.uk01603 286611

Oxford University Hospital

Oxford, United Kingdom

Recruiting
Hospital R&D contact (matched)

Shahista Hussain

ouhtma@ouh.nhs.uk---

University Hospitals Plymouth NHS Trust

Plymouth, United Kingdom

Recruiting
Hospital R&D contact (matched)

R&D Manager

plh-tr.RD-office@nhs.net01752 431776

Salisbury NHS Foundation Trust

Salisbury, United Kingdom

Recruiting
Hospital R&D contact (matched)

Kate Ames

sft.sftresearch@nhs.net01722 336262

Torbay & Newton Abbot Hospital

Torquay, United Kingdom

Recruiting

Royal Cornwall Hospital

Truro, United Kingdom

Recruiting
Hospital R&D contact (matched)

Abi Weeks

rch-tr.CornwallResearch@nhs.net01872 25 6424

Hampshire Hospitals NHS Foundation Trust

Winchester, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research Manager

research.team@hhft.nhs.uk01256 473202 Ext 4557

How to Get in Touch

RAINBOW Trial Coordinator

Sponsor contact

CONTACT

020 7679 9711 ctc.rainbow@ucl.ac.uk

UCL CTC haematology trials team

Sponsor contact

CONTACT

020 7679 9860
Data sourced from ClinicalTrials.gov · Last verified: 2024-05