Patient Guide: A Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Adults With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 16 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06973187
Status: 🟢 Enrolling Now
Condition: Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma
Phase: PHASE3

Where You Can Participate

This study is available at 16 locations across the country.

Top locations include:
  • • Jacksonville, Florida
  • • Dayton, Ohio
  • • Roanoke, Virginia
  • • And 13 more locations

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A Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Adults With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma - Join Clinical Trial NCTNCT06973187

How to Join This Clinical Trial - NCTNCT06973187

Learn how to participate in this PHASE3 trial studying an investigational therapy for Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06973187 - 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 16 locations. Find a study site near you:

Clinical Research Site

Jacksonville, Florida 001625 - United States

Status: RECRUITING

Clinical Research Site

Dayton, Ohio 45415 - United States

Status: RECRUITING

Clinical Research Site

Roanoke, Virginia 24014 - United States

Status: RECRUITING

Clinical Research Site

Spokane, Washington 99208-1129 - United States

Status: RECRUITING

Clinical Research Site

Tacoma, Washington 98405 - United States

Status: RECRUITING

Clinical Research Site

Concord, New South Wales NSW 2139 - Australia

Status: RECRUITING

Clinical Research Site

Birtinya, Queensland QLD 4575 - Australia

Status: RECRUITING

Clinical Research Site

Frankston, Victoria VIC 3199 - Australia

Status: RECRUITING

Clinical Research Site

Malvern East, Victoria VIC 3144 - Australia

Status: RECRUITING

Clinical Research Site

Melbourne, Victoria VIC 3000 - Australia

Status: RECRUITING

And 6 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 Chronic Lymphocytic Leukemia, Small Lymphocytic 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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