Patient Guide: A Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of Forimtamig in Participants With Relapsed or Refractory Multiple Myeloma (r/r MM)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 20 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04557150
Status: ACTIVE_NOT_RECRUITING
Condition: Multiple Myeloma
Phase: PHASE1

Where You Can Participate

This study is available at 20 locations across the country.

Top locations include:
  • • Melbourne, Victoria
  • • Ghent,
  • • København Ø,
  • • And 17 more locations

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A Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of Forimtamig in Participants With Relapsed or Refractory Multiple Myeloma (r/r MM) - Join Clinical Trial NCTNCT04557150

How to Join This Clinical Trial - NCTNCT04557150

Learn how to participate in this PHASE1 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
PHASE1 - Early safety study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04557150 - 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 20 locations. Find a study site near you:

Clinical Research Site

Melbourne, Victoria 3000 - Australia

Status: Contact for availability

Clinical Research Site

Ghent, 9000 - Belgium

Status: Contact for availability

Clinical Research Site

København Ø, 2100 - Denmark

Status: Contact for availability

Clinical Research Site

Odense C, 5000 - Denmark

Status: Contact for availability

Clinical Research Site

Lille, 59037 - France

Status: Contact for availability

Clinical Research Site

Nantes, 44093 - France

Status: Contact for availability

Clinical Research Site

Pessac, 33604 - France

Status: Contact for availability

Clinical Research Site

Napoli, Campania 80131 - Italy

Status: Contact for availability

Clinical Research Site

Bologna, Emilia-Romagna 40138 - Italy

Status: Contact for availability

Clinical Research Site

Milan, Lombardy 20133 - Italy

Status: Contact for availability

And 10 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 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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