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NCT06477783Recruiting

Study on the Clinical Efficacy of Teclistamab and Talquetamab

Prospective Observational Study on the Clinical Efficacy of Teclistamab and Talquetamab in Patients With Relapsed and Refractory Multiple Myeloma in Belgium

Source: ClinicalTrials.gov · Last updated 25 Sept 2026

Brief summary (registry, in English)

The aim of this study is to assess the clinical efficacy of the anti-BCMA/CD3 bispecific antibody teclistamab and anti-GPRC5D/CD3 bispecific antibody talquetamab in a prospective, real-life setting in Belgium.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
14 May 2024
Start date
1 Dec 2024
Primary completion date
Sept 2027
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
NCT number
NCT06477783

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 1 Dec 2024 to the primary completion date, Sept 2027
  • 17 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has started teclistamab or talquetamab treatment \>28 days before intended screening visit.

Other

  • Inability or unwillingness to comply with the study protocol, including scheduled visits, treatment plans, or follow-up requirements.

Who the study is looking for

  • Age 18 years or older
  • Written informed consent
  • Has a diagnosis of relapsed and refractory multiple myeloma
  • Has already received at least three previous treatments
  • Is refractory to at least 1 proteasome inhibitor, at least 1 immunomodulatory agent, and an anti-CD38 monoclonal antibody
  • Evidence of disease progression on the last line of therapy, based on determination of response by the IMWG response criteria
  • Anticipated to start treatment with teclistamab or talquetamab per routine clinical care or has started with teclistamab treatment ≤28 days before intended screening visit

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

Full criteria on ClinicalTrials.gov

Sites (17)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Imelda
Coordinator of this site? Confirm its status
BonheidenBelgiumNot yet recruiting
Institut Jules Bordet
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BrusselsBelgiumRecruiting
UCL - Saint Luc
Coordinator of this site? Confirm its status
BrusselsBelgiumRecruiting
Grand Hopital de Charleroi
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CharleroiBelgiumRecruiting
Universitair Ziekenhuis Antwerpen (Uza)
Coordinator of this site? Confirm its status
EdegemBelgiumRecruiting
Universitair Ziekenhuis Gent (Uz Gent)
Coordinator of this site? Confirm its status
GhentBelgiumRecruiting
Algemeen Ziekenhuis Maria Middelares (AZMM)
Coordinator of this site? Confirm its status
GhentBelgiumRecruiting
JESSA Ziekenhuis
Coordinator of this site? Confirm its status
HasseltBelgiumRecruiting
Epicura
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HornuBelgiumRecruiting
AZ Groeninge
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KortrijkBelgiumRecruiting
UZ Leuven Gasthuisberg
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LeuvenBelgiumRecruiting
CHU Liège
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LiègeBelgiumRecruiting
CHR Citadelle
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LiègeBelgiumRecruiting
CHU Ambroise Paré
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MonsBelgiumRecruiting
AZ Delta
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RoeselareBelgiumRecruiting
Vitaz
Coordinator of this site? Confirm its status
Sint-NiklaasBelgiumRecruiting
Chu Ucl Namur
Coordinator of this site? Confirm its status
YvoirBelgiumRecruiting

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