Patient Guide: 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

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 148 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06742996
Status: 🟢 Enrolling Now
Condition: Mantle Cell Lymphoma, B Cell Lymphoma
Phase: PHASE3

Where You Can Participate

This study is available at 148 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Phoenix, Arizona
  • • New Haven, Connecticut
  • • And 145 more locations

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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 - Join Clinical Trial NCTNCT06742996

How to Join This Clinical Trial - NCTNCT06742996

Learn how to participate in this PHASE3 trial studying an investigational therapy for Mantle Cell Lymphoma, B Cell Lymphoma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Mantle Cell Lymphoma, B Cell Lymphoma. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Mantle Cell Lymphoma, B Cell Lymphoma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06742996 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 148 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35294-0004 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Phoenix, Arizona 85054-4502 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

New Haven, Connecticut 06520-8028 - United States

Status: RECRUITING

Clinical Research Site

Pembroke Pines, Florida 33026-4119 - United States

Status: RECRUITING

Clinical Research Site

Weston, Florida 33331-3609 - United States

Status: RECRUITING

Clinical Research Site

Chicago, Illinois 60612 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Fort Wayne, Indiana 46804 - United States

Status: RECRUITING

Clinical Research Site

Waukee, Iowa 50263 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Baltimore, Maryland 21201-1544 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Boston, Massachusetts 02215-5418 - United States

Status: RECRUITING

And 138 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Mantle Cell Lymphoma, B Cell Lymphoma:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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