Sonrotoclax, Zanubrutinib and Rituximab in Previously Untreated Patients With Follicular Lymphoma

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorSun Yat-sen University

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • Sotoclax in combination with zanubrutinib and rituximab regimen

    Drug

    Zanubrutinib oral administration, Sotoclax oral administration, Rituximab intravenous injection.

Treatment groups

52 Participants
are divided into 1 treatment group
Group A: Experimental GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

CR rate

Complete response rate

Time frame
Up to 6 months

Secondary outcomes

1

ORR

Overall response rate

Time frame
Up to 6 months
2

DoR

Duration of response

Time frame
Up to 3 years
3

PFS

Progression free survival

Time frame
Up to 3 years
4

OS

Overall survival

Time frame
Up to 3 years

Other outcomes

1

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.

Time frame
Up to 3 years

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: