Patient Guide: Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Previously Untreated Follicular Lymphoma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 247 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06191744
Status: 🟢 Enrolling Now
Condition: Follicular Lymphoma (FL)
Phase: PHASE3

Where You Can Participate

This study is available at 247 locations across the country.

Top locations include:
  • • San Diego, California
  • • Santa Barbara, California
  • • Boulder, Colorado
  • • And 244 more locations

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Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Previously Untreated Follicular Lymphoma - Join Clinical Trial NCTNCT06191744

How to Join This Clinical Trial - NCTNCT06191744

Learn how to participate in this PHASE3 trial studying an investigational therapy for Follicular Lymphoma (FL). This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Follicular Lymphoma (FL). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Follicular Lymphoma (FL)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06191744 - 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 247 locations. Find a study site near you:

Clinical Research Site

San Diego, California 92103 - United States

Status: RECRUITING

Clinical Research Site

Santa Barbara, California 93105 - United States

Status: RECRUITING

Clinical Research Site

Boulder, Colorado 80303 - United States

Status: RECRUITING

Clinical Research Site

Newark, Delaware 19713 - United States

Status: RECRUITING

Clinical Research Site

Jacksonville, Florida 32256 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32803 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32806 - United States

Status: RECRUITING

Clinical Research Site

Coeur d'Alene, Idaho 83814 - United States

Status: RECRUITING

Clinical Research Site

Chicago, Illinois 60611-4494 - United States

Status: RECRUITING

Clinical Research Site

Decatur, Illinois 62526 - United States

Status: RECRUITING

And 237 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 Follicular Lymphoma (FL):

  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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