Patient Guide: Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 144 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04246047
Status: ACTIVE_NOT_RECRUITING
Condition: Multiple Myeloma
Phase: PHASE3

Where You Can Participate

This study is available at 144 locations across the country.

Top locations include:
  • • Yuma, Arizona
  • • Denver, Colorado
  • • Fairfield, Connecticut
  • • And 141 more locations

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Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma - Join Clinical Trial NCTNCT04246047

How to Join This Clinical Trial - NCTNCT04246047

Learn how to participate in this PHASE3 trial studying an investigational therapy for Multiple Myeloma. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Multiple Myeloma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04246047 - 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 144 locations. Find a study site near you:

Clinical Research Site

Yuma, Arizona 85364 - United States

Status: Contact for availability

Clinical Research Site

Denver, Colorado 80218 - United States

Status: Contact for availability

Clinical Research Site

Fairfield, Connecticut 45242 - United States

Status: Contact for availability

Clinical Research Site

Kansas City, Kansas 66205 - United States

Status: Contact for availability

Clinical Research Site

Tyler, Texas 75702 - United States

Status: Contact for availability

Clinical Research Site

Roanoke, Virginia 24014 - United States

Status: Contact for availability

Clinical Research Site

Camperdown, New South Wales 2050 - Australia

Status: Contact for availability

Clinical Research Site

Liverpool, New South Wales 2170 - Australia

Status: Contact for availability

Clinical Research Site

St Leonards, New South Wales 2065 - Australia

Status: Contact for availability

Clinical Research Site

Waratah, New South Wales 2298 - Australia

Status: Contact for availability

And 134 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 Multiple Myeloma:

  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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