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Tests a new PET/MR scan with a tracer to image multiple myeloma

Tests a new combined scan using a tracer in adults with multiple myeloma.

Plain-language title generated from the registry record
Registry title: PET/MR Scan With [68Ga]Ga-PentixaFor (CXCR4) vs Standard of Care (SOC) for Initial Staging and Follow up in Multiple Myeloma (MM)

Key facts

Where
Toronto, CanadaSee the site

Where in Canada

  • University Health NetworkToronto, CanadaTaking people

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Trial details

Who runs it
University Health Network, Toronto
Trial code
NCT06871176
Record updated
1 October 2026
Original description
Multiple myeloma is a disease mainly located in participants bones. Usually a participants physician arrives at this diagnosis by doing blood tests and ordering standard of care imaging tests (18F-FDG PET/CT and maybe additional MRI) to see how many bones (and/or other organs) are affected. While these two imaging tests are already very good, recent research indicates that even more precise imaging methods could be used to diagnose participants disease more precisely.Read full original descriptionShow less

[68Ga]Ga-PentixaFor (CXCR4) PET/MR for Initial Staging and Follow up in Multiple Myeloma: Prospective Comparison With Standard of Care PET/CT and Evaluation of Therapy Influence

Multiple myeloma is a disease mainly located in participants bones. Usually a participants physician arrives at this diagnosis by doing blood tests and ordering standard of care imaging tests (18F-FDG PET/CT and maybe additional MRI) to see how many bones (and/or other organs) are affected. While these two imaging tests are already very good, recent research indicates that even more precise imaging methods could be used to diagnose participants disease more precisely.

The purpose of this study is to learn if a combined PET/MR scan with a new radiotracer, [68Ga]Ga-PentixaFor, can provide more accurate and precise diagnostic information in patients with Multiple Myeloma, a type of cancer primarily affecting the bones.

This study aims to improve the accuracy of diagnosing and monitoring Multiple Myeloma using more advanced imaging techniques.

Inclusion: Patient older than 18 years of age; Clinical diagnosis of (nonsecretory, oligosecretory, suspicion for extramedullary MM) MM. MM diagnosis is based on IMWG (International Myeloma Working Group) criteria.No treatment received beyond first course of.

Exclusion: Any hypersensitivity or known allergy to any component of the investigational product ([68Ga]Ga-PentixaFor)No concomitant other malignant hemato-oncological disease being diagnosed (i.e. additional lymphoma or leukemia); Any contra-indications for MRI or 18F-FDG PET/CT imaging according to institutional guideline; Pregnancy (will be ruled out as per institutional protocol); Inability to lie still in prone position in MRI for at least 30 min or PET/CT for at least 30 min; Patients or unwilling to use contraception during study and breastfeeding women can also not partake in this study; Inability to provide consent.

ClinicalTrials.gov NCT06871176