Condition: Multiple Myeloma · Sponsor: Intergroupe Francophone du Myelome
200 adult patients with multiple myeloma receiving teclistamb will be included. Effectiveness, safety, and condition of use of teclistamab in early access program (post-MA) will be assessed. Primary objective is the evaluation of overall response rate (ORR) of teclistamab according to IMWG criteria. This is a multicenter, prospective, observational study.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| CHU Amiens Picardie | Amiens, France | — |
| CH d'ANNECY | Annecy, France | — |
| Centre hospitalier d'Argenteuil | Argenteuil, France | — |
| Hopital de la cote Basque | Bayonne, France | — |
| CHU de Besançon | Besançon, France | — |
| CHU Bordeaux | Bordeaux, France | — |
| Centre hospitalier de Brive-la-Gaillarde | Brive-la-Gaillarde, France | — |
| CHU CAEN | Caen, France | — |
| Centre hospitalier Métropole de Savoie | Chambéry, France | — |
| CHU Clermont-Ferrand Site Estaing | Clermont-Ferrand, France | — |
| CHU Henri Mondor | Créteil, France | — |
| Chu Dijon | Dijon, France | — |
+ 19 more locations — full list on the registry record.
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