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2022-501811-14-00RecruitingPhase 1/2

[68Ga]Ga-PentixaFor positron emission tomography for improved risk and disease assessment in myeloma

Source: EU CTIS (euclinicaltrials.eu) · Last updated 2 Sept 2026

Next steps

Brief summary (registry, in English)

To evaluate the proportion of false negative (FN) PET results for [68Ga]Ga-PentixaFor PET/AC-CT at baseline.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
90 (estimated)
First submitted
24 Mar 2023
Start date
20 Sept 2024
Lead sponsor
University Of Antwerp
EU CT number
2022-501811-14-00

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 90
  • 4 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with newly diagnosed multiple myeloma who are planned for induction chemotherapy followed by a stem-cell transplant (ASCT). It tests a [68Ga]Ga-PentixaFor PET scan.

Age
18 years or older.
Sex
All sexes can join.
Disease stage
Newly diagnosed multiple myeloma by current IMWG criteria, scheduled for induction chemotherapy followed by ASCT. WHO performance status 0-2; above 2 may be allowed if fit for intensive chemotherapy in the physician's opinion. Life expectancy over 12 months.
Earlier treatment
No induction chemotherapy yet: the [68Ga]Ga-PentixaFor PET/CT must be scheduled before it starts.
Biomarker or test result
A baseline 18F-FDG PET/CT scan is needed. The [68Ga]Ga-PentixaFor scan must come at most 14 days from the 18F-FDG scan.

Main reasons for not taking part

  • A condition that may affect following the study, such as severe claustrophobia or not being able to lie still for 30 minutes
  • Another cancer, except non-melanoma skin cancer, carcinoma in situ of the cervix, or a cancer treated and in remission for more than 5 years
  • Pregnant or breastfeeding
  • Refusal or inability to give written informed consent

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of concomitant presence of any other malignancy, except for: non-melanoma skin cancer, carcinoma in situ of the cervix, or any other effectively treated malignancy that has been in remission for >5 years or that is highly likely to be cured at the time of enrollment.

Other illness

  • Any physical or physiological condition that may affect adherence to the study protocol, e.g severe claustrophobia or the inability to lie still for 30 minutes.

Other

  • Pregnant or breastfeeding
  • Refusal or inability to provide written informed consent

Who the study is looking for

  • Transplant-eligible newly diagnosed multiple myeloma based on current IMWG criteria and scheduled for induction chemotherapy followed by ASCT.
  • Baseline 18F-FDG PET/CT scan
  • WHO performance status 0-2 (WHO > 2 can be allowed if the patient is fit for intensive chemotherapy based on the opinion of the physician).
  • 18 years of older.
  • Signed informed consent.
  • Life expectancy > 12 months, based on clinical judgement.
  • Baseline [68Ga]Ga-PentixaFor PET/CT should be scheduled before starting induction chemotherapy.
  • An interval of maximum 14 days is allowed between the 18F-FDG and [68Ga]Ga-PentixaFor PET/CT scans (Specific for this study).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (4)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Antwerp University HospitalEdegemBelgiumRecruiting
Universitair Ziekenhuis GentGentBelgiumRecruiting
UZ LeuvenLeuvenBelgiumRecruiting
Amsterdam UMCAmsterdamNetherlandsNot yet recruiting

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.