Patient Guide: A Study to Customize Ibrutinib Treatment Regimens for Participants With Previously Untreated Chronic Lymphocytic Leukemia

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 74 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05963074
Status: 🟢 Enrolling Now
Condition: Leukemia, Leukemia, Lymphoid, Leukemia, Lymphocytic, Chronic, B-Cell
Phase: PHASE2

Where You Can Participate

This study is available at 74 locations across the country.

Top locations include:
  • • Cerritos, California
  • • Los Alamitos, California
  • • San Luis Obispo, California
  • • And 71 more locations

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A Study to Customize Ibrutinib Treatment Regimens for Participants With Previously Untreated Chronic Lymphocytic Leukemia - Join Clinical Trial NCTNCT05963074

How to Join This Clinical Trial - NCTNCT05963074

Learn how to participate in this PHASE2 trial studying an investigational therapy for Leukemia, Leukemia, Lymphoid, Leukemia, Lymphocytic, Chronic, B-Cell. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Leukemia, Leukemia, Lymphoid, Leukemia, Lymphocytic, Chronic, B-Cell
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05963074 - 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 74 locations. Find a study site near you:

Clinical Research Site

Cerritos, California 90703 - United States

Status: RECRUITING

Clinical Research Site

Los Alamitos, California 90720 - United States

Status: RECRUITING

Clinical Research Site

San Luis Obispo, California 93401 - United States

Status: RECRUITING

Clinical Research Site

Santa Rosa, California 95403 - United States

Status: RECRUITING

Clinical Research Site

Whittier, California 90602 - United States

Status: RECRUITING

Clinical Research Site

Grand Junction, Colorado 81505 - United States

Status: RECRUITING

Clinical Research Site

Miami Beach, Florida 33140-2948 - United States

Status: RECRUITING

Clinical Research Site

North Miami Beach, Florida 33169 - United States

Status: RECRUITING

Clinical Research Site

Orange, Florida 32763 - United States

Status: RECRUITING

Clinical Research Site

Boise, Idaho 83702 - United States

Status: RECRUITING

And 64 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 Leukemia, Leukemia, Lymphoid, Leukemia, Lymphocytic, Chronic, B-Cell:

  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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