Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

A Study to Investigate the Efficacy and Safety of Sonrotoclax Plus Zanubrutinib Compared With Placebo Plus Zanubrutinib in Adults With Relapsed/Refractory Mantle Cell Lymphoma (CELESTIAL-RRMCL)

NCT06742996 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this study is to compare how well sonrotoclax plus zanubrutinib works versus zanubrutinib plus placebo in treating adults with relapsed/refractory (R/R) mantle cell lymphoma (MCL). This study will also look at the safety of sonrotoclax plus zanubrutinib versus zanubrutinib plus placebo.

Interventions

  • DRUG Zanubrutinib
  • DRUG Sonrotoclax
  • DRUG Placebo

Study Locations (20)

Florida

  • Memorial Cancer Institute, Memorial Healthcare System — Pembroke Pines
  • Cleveland Clinic Florida — Weston

Michigan

  • University of Michigan — Ann Arbor
  • The Cancer and Hematology Centers — Grand Rapids

Nebraska

  • Nebraska Cancer Specialists St Francis Grand Island — Grand Island
  • Nebraska Cancer Specialists — Omaha

North Carolina

  • Atrium Health Levine Cancer Institute (Lci) — Charlotte
  • Duke University — Durham

Alabama

  • University of Alabama At Birmingham Hospital — Birmingham

Arizona

  • Mayo Clinic Phoenix — Phoenix

Connecticut

  • Yale University, Yale Cancer Center — New Haven

Illinois

  • Rush University Medical Center — Chicago

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2025-03-05
Est. Completion 2032-03-30
Phase Phase 3

Sponsor

BeOne Medicines

138 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06742996

The ClinicalTrials.gov registry entry for NCT06742996 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BeOne Medicines, which has 138 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Mantle Cell Lymphoma appearing as the primary indexed condition, and to 3 interventions — of which Zanubrutinib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06742996 reports 20 study locations spanning 16 distinct geographic areas — top geographies include Florida, Michigan, Nebraska. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06742996 about?

NCT06742996 is a clinical study titled "A Study to Investigate the Efficacy and Safety of Sonrotoclax Plus Zanubrutinib Compared With Placebo Plus Zanubrutinib in Adults With Relapsed/Refractory Mantle Cell Lymphoma (CELESTIAL-RRMCL)". The goal of this study is to compare how well sonrotoclax plus zanubrutinib works versus zanubrutinib plus placebo in treating adults with relapsed/refractory (R/R) mantle cell lymphoma (MCL). This study will also look at the safety of sonrotoclax plus zanubrutinib versus zanubrutinib plus placebo.

What is the current status of trial NCT06742996?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 300 participants. The study started on 2025-03-05. Estimated completion is 2032-03-30.

What conditions does trial NCT06742996 study?

This clinical trial studies the following conditions: Mantle Cell Lymphoma, B Cell Lymphoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06742996?

The interventions under investigation include: Zanubrutinib (DRUG), Sonrotoclax (DRUG), Placebo (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06742996?

This trial is sponsored by BeOne Medicines, which has 138 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06742996 being conducted?

This trial has 20 study locations across Alabama, Arizona, Connecticut, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial