Patient Guide: A Study to Evaluate the Effect of Venetoclax on Participants Receiving a Covalent Bruton's Tyrosine Kinase Inhibitor (cBTKi) for First-line Chronic Lymphocytic Leukemia (1L CLL) to Achieve Deep Durable Remissions to Allow Off-treatment Period.

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 21 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06524375
Status: 🟢 Enrolling Now
Condition: Chronic Lymphocytic Leukemia
Phase: PHASE2

Where You Can Participate

This study is available at 21 locations across the country.

Top locations include:
  • • Springdale, Arkansas
  • • Aurora, Colorado
  • • Jacksonville, Florida
  • • And 18 more locations

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A Study to Evaluate the Effect of Venetoclax on Participants Receiving a Covalent Bruton's Tyrosine Kinase Inhibitor (cBTKi) for First-line Chronic Lymphocytic Leukemia (1L CLL) to Achieve Deep Durable Remissions to Allow Off-treatment Period. - Join Clinical Trial NCTNCT06524375

How to Join This Clinical Trial - NCTNCT06524375

Learn how to participate in this PHASE2 trial studying an investigational therapy for Chronic Lymphocytic Leukemia. 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. 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
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06524375 - 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 21 locations. Find a study site near you:

Clinical Research Site

Springdale, Arkansas 72762 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80012-5405 - United States

Status: RECRUITING

Clinical Research Site

Jacksonville, Florida 32256-6932 - United States

Status: RECRUITING

Clinical Research Site

Athens, Georgia 30607 - United States

Status: RECRUITING

Clinical Research Site

Fort Wayne, Indiana 46804 - United States

Status: RECRUITING

Clinical Research Site

Des Moines, Iowa 50314-3030 - United States

Status: RECRUITING

Clinical Research Site

Bethesda, Maryland 20817-1915 - United States

Status: RECRUITING

Clinical Research Site

Boston, Massachusetts 02215-5418 - United States

Status: RECRUITING

Clinical Research Site

Grand Island, Nebraska 68803 - United States

Status: RECRUITING

Clinical Research Site

Omaha, Nebraska 68130-2042 - United States

Status: RECRUITING

And 11 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Chronic Lymphocytic Leukemia:

  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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