Etude de Phase III, randomisée, ouverte, internationale, multicentrique, évaluant l’efficacité et la tolérance du mosunetuzumab associé au lénalidomide versus un anticorps monoclonal anti-CD20 associé à une chimiothérapie chez des patients atteints d’un lymphome folliculaire FLIPI 2-5 non préalablement traité

[Code officiel acronyme : MO44842 - MorningLyte]

Date d'ouverture : 07/10/2024

Investigateur : BIJOU F.

Domaine : III

Phase : Ouvert aux inclusions

Statut : LYSARC

Intervention : médicament

Population : lymphome folliculaire

Promoteur : Rechercheclinique@bordeaux.unicancer.fr

Spécialité : Hématologie

BIJOU F.

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