About this trial
Follicular lymphoma (FL) remains an incurable indolent B-cell lymphoma for many patients, and although rituximab-based chemoimmunotherapy can achieve high initial response rates, a substantial proportion of patients experience early progression, including POD24, which is associated with poor long-term outcomes. This underscores the need for more effective and better-tolerated frontline treatment strategies, particularly chemotherapy-free approaches. The present study is based on a strong biologic rationale that simultaneously targets two key pathogenic mechanisms in FL: aberrant B-cell receptor signaling and impaired apoptosis driven by BCL2 overexpression. Zanubrutinib, a next-generation BTK inhibitor, has shown clinical activity with a favorable safety profile in FL, while sonrotoclax, a potent and highly selective next-generation BCL2 inhibitor, has demonstrated promising preclinical and early clinical activity. In combination with rituximab, this chemotherapy-free triplet regimen may produce deeper and more durable remissions while maintaining manageable toxicity, and therefore has the potential to expand frontline treatment options and improve outcomes for patients with previously untreated FL.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Willing to participate in the clinical study and signed informed consent.
Age ≥18 years, no gender restrictions.
Pathologically diagnosed with follicular lymphoma (Grade 1, 2, or 3a) and previously untreated.
Has at least one measurable or assessable lesion.
Disqualifiers
Known active central nervous system lymphoma or leptomeningeal disease.
Evidence of follicular lymphoma with transformation to diffuse large B-cell lymphoma.
Prior history of other malignancies other than follicular lymphoma (except for those with disease-free survival ≥5 years and assessed by the investigator as having low risk of recurrence).
History of allergy to the investigational drug, similar drugs, or excipients.
Trial design
Single group
Treatments tested in this trial
Sotoclax in combination with zanubrutinib and rituximab regimen
DrugZanubrutinib oral administration, Sotoclax oral administration, Rituximab intravenous injection.
Treatment groups
Trial outcomes
Primary outcomes
CR rate
Complete response rate
Secondary outcomes
ORR
Overall response rate
DoR
Duration of response
PFS
Progression free survival
OS
Overall survival
Other outcomes
Exploratory Analysis of Biomarkers and Mechanisms Related to Efficacy and Safety
Tumor tissue and peripheral blood samples will be analyzed using multi-omics approaches to explore biomarkers and biological mechanisms associated with efficacy and safety.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: