Patient Guide: A Study to Investigate Subcutaneous Isatuximab in Combination With Weekly Carfilzomib and Dexamethasone in Adult Participants With Relapsed and/or 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 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: NCTNCT06356571
Status: 🟢 Enrolling Now
Condition: Plasma Cell Myeloma Refractory
Phase: PHASE2

Where You Can Participate

This study is available at 22 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • West Hollywood, California
  • • New Haven, Connecticut
  • • And 19 more locations

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A Study to Investigate Subcutaneous Isatuximab in Combination With Weekly Carfilzomib and Dexamethasone in Adult Participants With Relapsed and/or Refractory Multiple Myeloma - Join Clinical Trial NCTNCT06356571

How to Join This Clinical Trial - NCTNCT06356571

Learn how to participate in this PHASE2 trial studying an investigational therapy for Plasma Cell Myeloma Refractory. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Plasma Cell Myeloma Refractory
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06356571 - 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

Phoenix, Arizona 85054 - United States

Status: RECRUITING

Clinical Research Site

West Hollywood, California 90069 - United States

Status: RECRUITING

Clinical Research Site

New Haven, Connecticut 06511 - United States

Status: RECRUITING

Clinical Research Site

Jacksonville, Florida 32224 - United States

Status: RECRUITING

Clinical Research Site

Margate, Florida 33063 - United States

Status: RECRUITING

Clinical Research Site

Pembroke Pines, Florida 33024 - United States

Status: RECRUITING

Clinical Research Site

Plantation, Florida 33322 - United States

Status: RECRUITING

Clinical Research Site

Covington, Louisiana 70433 - United States

Status: RECRUITING

Clinical Research Site

Dearborn, Michigan 48126 - United States

Status: RECRUITING

Clinical Research Site

Royal Oak, Michigan 48073 - United States

Status: RECRUITING

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 Plasma Cell Myeloma Refractory:

  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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