Groupe d'Etude en Oncologie du Quebec

Titre	Study to Describe the Management and the Use of Healthcare Resources in Patients With Chronic Lymphocytic Leukemia (CLL) Initiating Venetoclax in Routine Clinical Practice
Protocole ID	P16-489 (DEVOTE)
ClinicalTrials.gov ID	NCT03310190
Type(s) de cancer	Leucémie lymphoïde chronique (LLC)
Phase	Autres
Médicament	venetoclax
Institution	CISSS DU BAS-SAINT-LAURENT HOPITAL REGIONAL DE RIMOUSKI 150 av. Rouleau, Rimouski, QC, G5L 5T1
Ville	Rimouski
Investigateur(trice) principal(e)	Dre Marie-Pierre Bernard
Coordonnateur(trice)	Julie Levesque 418-724-3000 poste 8029
Statut	Fermé
Critètes d'éligibilité	Patient's physician prescribed venetoclax as per product monograph independent of the patient participation in this study. Has chronic lymphocytic leukemia (CLL) with deletion of the short arm of chromosome (17del[17p]) who have received at least 1 prior therapy, or CLL without del(17p) who have received at least one prior therapy and for whom there are no other available treatment options.
Critètes d'exclusion	Currently participating in an interventional study. Using strong CYP3A inhibitors. Has other condition that, in the opinion of the treating physician, prohibits the patient from participating in the study or obscures the assessment of the treatment of CLL. Is pregnant or not using appropriate means of contraception.

Groupe d'étude en oncologie du Québec