Clinical trial · Interventional
Zanubrutinib, Ixazomib and Dexamethasone in Patients With Treatment Naive Waldenstrom's Macroglobulinemia
A Phase 2 Clinical Trial to Evaluate the Efficacy of Zanubrutinib Plus Ixazomib and Dexamethasone in Newly Diagnosed Symptomatic Waldenström Macroglobulinemia
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to evaluate the efficacy of BTK inhibitor Zanubrutinib combined with Ixazomib and Dexamethasone (ZID) for the newly diagnosed Waldenstrom Macroglobulinemia. This ZID regimen will be given up to 24 months and stopped for observation. We propose this combination will improve the deep remission (≥VGPR) compared to single Zanubrutinib or IRD regimen and can be a time-limited regimen which will reduce the life-time therapy and benefit the patients.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Waldenström Macroglobulinemia | Waldenstrom Macroglobulinemia | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Zanubrutinib,Ixazomib and Dexamethasone | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- ZID regimen
- description
- Zanubrutinib, 160mg orally, twice a day; Ixazomib, 4 mg orally, day 1, 8, 15; Dexamethasone, 20mg orally, days 1, 8, 15.
- interventionNames
- Drug: Zanubrutinib,Ixazomib and Dexamethasone
Primary outcomes (1)
- measure
- Deep remission response rate
- timeFrame
- up to 5 years
- description
- ≥VGPR after 6 cycles introduction
Secondary outcomes (6)
- measure
- Complete response (CR)
- timeFrame
- up to 12 months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. The gender of the patient is not limited, and the age is ≥18 years old; 2. Must meet WM's diagnostic standards; 3. The patient is an untreated or patient who has not undergone standard treatment. The specific conditions are as follows: 1. No combined chemotherapy with BR, RCD, VRD, CHOP and COP 2. No treatment regimen containing fludarabine 3. Chlorambucil or cyclophosphamide for less than 4 weeks (alone or in combination with adrenal glucocorticoids) 4. The above treatment did not reach the treatment response (MR) 5. If the above treatment has been applied, the treatment needs to be stopped for 2 weeks before entering the group to start treatment 4. The indications for the treatment of indolent lymphoma mainly include (at least one of the following conditions): 1. Symptomatic hyperviscosity; 2. symptomatic peripheral neuropathy; 3. Amyloidosis; 4. Cold agglutinin disease; cryoglobulinemia; 5. Disease-related cytopenia (Hb\<100 g/L, PLT\<100×10\^9/L); 6. giant lymph nodes; 7. Those with systemic systemic symptoms: for two weeks/recurrent fever (above 38℃) and not caused by infection, or Night sweats and/or weight loss \>10% within 6 months; 8. The disease progresses rapidly, for example, the lymph nodes increase by more than 50% within 2 months, and/or peripheral blood lymphocytes absolute value doubling time \<6 months, and/or rapid hemoglobin or platelet non-autoimmune causes slow down 9. When there is evidence that the disease has transformed. 5. ECOG score ≤ 2 points 6. Laboratory examination: neutrophils ≥ 0.75×10\^9/L; platelets ≥ 50×10\^9/L; total bilirubin ≤ 2.5 times upper limit; alanine aminotransferase/aspartate aminotransferase ≤3 times upper limit. Creatinine clearance rate ≥ 30ml/min. 7. The patient's expected survival time is ≥ 3 months. Exclusion Criteria: 1. Malignant tumors (including active central nervous system lymphoma) other than B-NHL have been diagnosed or treated within the past year; 2. There is clinical evidence that large cell lymphoma transformation has occurred; 3. Non-lymphoma-related liver and kidney damage: alanine aminotransferase (ALT)\> 3 times the upper limit of normal value, aspartate aminotransferase (AST)\> 3 times the upper limit of normal value, total bilirubin (TBIL)\> upper limit of normal value 2 Times, serum creatinine clearance rate \<30ml/min; 4. Other serious medical conditions will affect the study (such as uncontrolled diabetes, gastric ulcers, other serious cardiopulmonary diseases, etc.). The decision-making power belongs to the researcher; 5. Known history of infection with human immunodeficiency virus (HIV) or active hepatitis B virus (HBV) infection, or any uncontrolled active systemic infection requiring intravenous antibiotics. 6. Central nervous system dysfunction with clinical manifestations or central invasion (Bing-Neel syndrome); 7. Patients who have undergone major surgery (not including lymph node biopsy) within the past 14 days or expected major surgery during treatment; 8. Inability to swallow capsules or suffer from malabsorption syndrome, diseases that significantly affect gastrointestinal function, have undergone gastric or small bowel resection, symptomatic inflammatory bowel disease or ulcerative colitis, partial or complete intestinal obstruction. 9. Need to receive strong cytochrome P450 (CYP) 3A inhibitor treatment. 10. Women who are pregnant or breastfeeding, women of childbearing age who have not taken contraception; 11. Allergy to the drugs used.
References
Publications (3)
- BACKGROUNDTreon SP, Xu L, Guerrera ML, Jimenez C, Hunter ZR, Liu X, Demos M, Gustine J, Chan G, Munshi M, Tsakmaklis N, Chen JG, Kofides A, Sklavenitis-Pistofidis R, Bustoros M, Keezer A, Meid K, Patterson CJ, Sacco A, Roccaro A, Branagan AR, Yang G, Ghobrial IM, Castillo JJ. Genomic Landscape of Waldenstrom Macroglobulinemia and Its Impact on Treatment Strategies. J Clin Oncol. 2020 Apr 10;38(11):1198-1208. doi: 10.1200/JCO.19.02314. Epub 2020 Feb 21. PMID 32083995
- BACKGROUNDTreon SP, Xu L, Hunter Z. MYD88 Mutations and Response to Ibrutinib in Waldenstrom's Macroglobulinemia. N Engl J Med. 2015 Aug 6;373(6):584-6. doi: 10.1056/NEJMc1506192. No abstract available. PMID 26244327
- BACKGROUNDCastillo JJ, Meid K, Gustine JN, Dubeau T, Severns P, Hunter ZR, Yang G, Xu L, Treon SP. Prospective Clinical Trial of Ixazomib, Dexamethasone, and Rituximab as Primary Therapy in Waldenstrom Macroglobulinemia. Clin Cancer Res. 2018 Jul 15;24(14):3247-3252. doi: 10.1158/1078-0432.CCR-18-0152. Epub 2018 Apr 16. PMID 29661775