26
Participants
Start Date
November 29, 2019
Primary Completion Date
October 22, 2024
Study Completion Date
November 1, 2024
Cabozantinib
All participants will be treated by 60 mg of cabozantinib once daily. Temporary or permanent discontinuation and/or dose reduction of cabozantinib therapy may be required for the management of some adverse reactions. When dose reduction is necessary, it is recommended to reduce to 40 mg daily, and then to 20 mg daily.
CHU Besancon, Besançon
IUCT-Institut Claudius Regaud, Toulouse
CHU Bordeaux, Bordeaux
Institut de Cancérologie de l'Ouest-site René Gauducheau, Saint-Herblain
Institut de Cancérologie de l'Ouest-Site Paul Papin, Angers
Institut de Cancérologie de la Lorraine, Nancy
Centre Jean Perrin, Clermont-Ferrand
ICANS, Strasbourg
Centre Leon Berard, Lyon
Hopital Européen Georges Pompidou, Paris
Hopital Foch, Suresnes
Institut Gustave Roussy, Villejuif
Centre Leon Berard
OTHER