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RECRUITING
NCT06477783

Study on the Clinical Efficacy of Teclistamab

Sponsor: Universitaire Ziekenhuizen KU Leuven

View on ClinicalTrials.gov

Summary

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

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2024-12-01

Completion Date

2027-09

Last Updated

2025-03-12

Healthy Volunteers

No

Interventions

DRUG

Teclistamab

Intervention is part of standard clinical care, as Tecvayli/Teclistamab is reimbursed for this group of patients.

Locations (17)

Imelda

Bonheiden, Antwerpen, Belgium

Universitair Ziekenhuis Antwerpen (UZA)

Edegem, Antwerpen, Belgium

Grand Hôpital de Charleroi

Charleroi, Henegouwen, Belgium

EpiCURA

Hornu, Henegouwen, Belgium

CHU Ambroise Paré

Mons, Henegouwen, Belgium

Jessa Ziekenhuis

Hasselt, Limburg, Belgium

CHR Citadelle

Liège, Liège, Belgium

CHU Liège

Liège, Liège, Belgium

CHU UCL Namur

Yvoir, Namur, Belgium

Algemeen Ziekenhuis Maria Middelares (AZMM)

Ghent, Oost-Vlaanderen, Belgium

Universitair Ziekenhuis Gent (UZ Gent)

Ghent, Oost-Vlaanderen, Belgium

Vitaz

Sint-Niklaas, Oost-Vlaanderen, Belgium

Institut Jules Bordet

Brussels, Vlaams-Brabant, Belgium

UCL Saint Luc

Brussels, Vlaams-Brabant, Belgium

AZ Groeninge

Kortrijk, West-Vlaanderen, Belgium

AZ Delta

Roeselare, West-Vlaanderen, Belgium

UZ Leuven Gasthuisberg

Leuven, Belgium