Patient Guide: A Study of Zilovertamab Vedotin (MK-2140) in Combination With Cyclophosphamide, Doxorubicin, and Prednisone Plus Rituximab or Rituximab Biosimilar (Truxima) (R-CHP) in Participants With Diffuse Large B-Cell Lymphoma (DLBCL) (MK-2140-007)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 22 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05406401
Status: ACTIVE_NOT_RECRUITING
Condition: Lymphoma, Large B-Cell, Diffuse (DLBCL)
Phase: PHASE2

Where You Can Participate

This study is available at 22 locations across the country.

Top locations include:
  • • Victoria, British Columbia
  • • Toronto, Ontario
  • • Montreal, Quebec
  • • And 19 more locations

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A Study of Zilovertamab Vedotin (MK-2140) in Combination With Cyclophosphamide, Doxorubicin, and Prednisone Plus Rituximab or Rituximab Biosimilar (Truxima) (R-CHP) in Participants With Diffuse Large B-Cell Lymphoma (DLBCL) (MK-2140-007) - Join Clinical Trial NCTNCT05406401

How to Join This Clinical Trial - NCTNCT05406401

Learn how to participate in this PHASE2 trial studying an investigational therapy for Lymphoma, Large B-Cell, Diffuse (DLBCL). Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Lymphoma, Large B-Cell, Diffuse (DLBCL)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05406401 - 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 22 locations. Find a study site near you:

Clinical Research Site

Victoria, British Columbia V8R 6V5 - Canada

Status: Contact for availability

Clinical Research Site

Toronto, Ontario L6R3J7 - Canada

Status: Contact for availability

Clinical Research Site

Montreal, Quebec H4J 1C5 - Canada

Status: Contact for availability

Clinical Research Site

Jerusalem, 9112001 - Israel

Status: Contact for availability

Clinical Research Site

Ramat Gan, 5265601 - Israel

Status: Contact for availability

Clinical Research Site

Roma, Lazio 00168 - Italy

Status: Contact for availability

Clinical Research Site

Milano, Lombardia 20132 - Italy

Status: Contact for availability

Clinical Research Site

Palermo, Sicilia 90146 - Italy

Status: Contact for availability

Clinical Research Site

Firenze, Toscana 50134 - Italy

Status: Contact for availability

Clinical Research Site

Alessandria, 15121 - Italy

Status: Contact for availability

And 12 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 Lymphoma, Large B-Cell, Diffuse (DLBCL):

  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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