Patient Guide: Long-Term Follow-up Study

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 30 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05332054
Status: ENROLLING_BY_INVITATION
Condition: Lymphoma, Multiple Myeloma, Lymphoma, Non-Hodgkin, Lymphoma, B-Cell, Hematologic Neoplasms
Phase: Not Specified

Where You Can Participate

This study is available at 30 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Gilbert, Arizona
  • • Scottsdale, Arizona
  • • And 27 more locations

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Long-Term Follow-up Study - Join Clinical Trial NCTNCT05332054

How to Join This Clinical Trial - NCTNCT05332054

Learn how to participate in this Not Specified trial studying an investigational therapy for Lymphoma, Multiple Myeloma, Lymphoma, Non-Hodgkin, Lymphoma, B-Cell, Hematologic Neoplasms. Current status: ENROLLING_BY_INVITATION.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Lymphoma, Multiple Myeloma, Lymphoma, Non-Hodgkin, Lymphoma, B-Cell, Hematologic Neoplasms
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT05332054 - 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 30 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35233 - United States

Status: Contact for availability

Clinical Research Site

Gilbert, Arizona 85234 - United States

Status: Contact for availability

Clinical Research Site

Scottsdale, Arizona 85258 - United States

Status: Contact for availability

Clinical Research Site

Irvine, California 92868 - United States

Status: Contact for availability

Clinical Research Site

La Jolla, California 92093 - United States

Status: Contact for availability

Clinical Research Site

Denver, Colorado 80045 - United States

Status: Contact for availability

Clinical Research Site

Denver, Colorado 80218 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33136 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32804 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30342 - United States

Status: Contact for availability

And 20 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Lymphoma, Multiple Myeloma, Lymphoma, Non-Hodgkin, Lymphoma, B-Cell, Hematologic Neoplasms:

  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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