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sdAb-based TRNT of Multiple Myeloma: a Feasibility Study (MUM)

U

Universitair Ziekenhuis Brussel

Status

Completed

Conditions

Multiple Myeloma

Treatments

Other: Blood sampling and bone marrow analysis

Study type

Interventional

Funder types

Other

Identifiers

NCT03956615
UZBRU_MUM

Details and patient eligibility

About

This study aims to show that antiidiotypic sdAb are a new, sensitive, specific and non-invasive tool for imaging and therapeutic purposes and provides a rationale for their clinical evaluation as a personalized treatment option for MM patients expressing surface paraprotein.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients will only be included in the study if they meet all of the following criteria:

  • Patients who have given informed consent
  • Patients at least 18 years old
  • Patients scheduled to undergo bone marrow sampling in clinical routine because of a clinically suspected or pathologically confirmed multiple myeloma.

Exclusion criteria

Patients will not be included in the study if one of the following criteria applies:

  • Patients who cannot communicate reliably with the investigator
  • Patients who are unlikely to cooperate with the requirements of the study
  • Patients at increased risk of death from a pre-existing concurrent illness
  • Patients who participated already in part I of this study

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Clinically Suspected or Pathologically Confirmed Multiple Myeloma.
Other group
Description:
Patients with a clinically suspected or pathologically confirmed multiple myeloma.
Treatment:
Other: Blood sampling and bone marrow analysis

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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