Patient Guide: A Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Mosunetuzumab + Lenalidomide (+Len), and the Safety, Tolerability, and Pharmacokinetics of SC Versus IV Mosunetuzumab + Len in Participants With Follicular Lymphoma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 28 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04246086
Status: 🟢 Enrolling Now
Condition: Follicular Lymphoma
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 28 locations across the country.

Top locations include:
  • • Duarte, California
  • • Cleveland, Ohio
  • • Cleveland, Ohio
  • • And 25 more locations

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A Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Mosunetuzumab + Lenalidomide (+Len), and the Safety, Tolerability, and Pharmacokinetics of SC Versus IV Mosunetuzumab + Len in Participants With Follicular Lymphoma - Join Clinical Trial NCTNCT04246086

How to Join This Clinical Trial - NCTNCT04246086

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Follicular Lymphoma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Follicular Lymphoma. 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
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT04246086 - 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 28 locations. Find a study site near you:

Clinical Research Site

Duarte, California 91010 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Cleveland, Ohio 44111 - United States

Status: RECRUITING

Clinical Research Site

Cleveland, Ohio 44195-0001 - United States

Status: RECRUITING

Clinical Research Site

Mayfield Heights, Ohio 44124 - United States

Status: RECRUITING

Clinical Research Site

Chattanooga, Tennessee 37404 - United States

Status: RECRUITING

Clinical Research Site

Franklin, Tennessee 37067 - United States

Status: RECRUITING

Clinical Research Site

Seattle, Washington 98122 - United States

Status: WITHDRAWN

Clinical Research Site

Changchun, 130021 - China

Status: RECRUITING

Clinical Research Site

Changsha City, 410013 - China

Status: WITHDRAWN

Clinical Research Site

Chengdu, 610041 - China

Status: RECRUITING

And 18 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Follicular 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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