Patient Guide: A Study to Evaluate the Optimization of the Cytokine Release Syndrome Profile for Glofitamab in Combination With Gemcitabine Plus Oxaliplatin in Participants With Relapsed/Refractory Diffuse Large B-Cell Lymphoma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 48 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06806033
Status: 🟢 Enrolling Now
Condition: Diffuse Large B-Cell Lymphoma
Phase: PHASE2

Where You Can Participate

This study is available at 48 locations across the country.

Top locations include:
  • • Anchorage, Alaska
  • • Fullerton, California
  • • Glendale, California
  • • And 45 more locations

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A Study to Evaluate the Optimization of the Cytokine Release Syndrome Profile for Glofitamab in Combination With Gemcitabine Plus Oxaliplatin in Participants With Relapsed/Refractory Diffuse Large B-Cell Lymphoma - Join Clinical Trial NCTNCT06806033

How to Join This Clinical Trial - NCTNCT06806033

Learn how to participate in this PHASE2 trial studying an investigational therapy for Diffuse Large 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 Diffuse Large 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
Diffuse Large B-Cell Lymphoma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06806033 - 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 48 locations. Find a study site near you:

Clinical Research Site

Anchorage, Alaska 99508 - United States

Status: RECRUITING

Clinical Research Site

Fullerton, California 92835 - United States

Status: RECRUITING

Clinical Research Site

Glendale, California 91204 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90067 - United States

Status: RECRUITING

Clinical Research Site

San Francisco, California 94110 - United States

Status: RECRUITING

Clinical Research Site

Torrance, California 90502-2006 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80012 - United States

Status: RECRUITING

Clinical Research Site

Gainesville, Florida 32608 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33140 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32806 - United States

Status: RECRUITING

And 38 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 Diffuse Large 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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