Groupe d'Etude en Oncologie du Quebec

Titre	A Phase 3 Randomized Study Comparing Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) Followed by Ciltacabtagene Autoleucel Versus Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) Followed by Autologous Stem Cell Transplant (ASCT) in Participants With Newly Diagnosed Multiple Myeloma Who Are Transplant Eligible
Protocole ID	CARTITUDE-6
ClinicalTrials.gov ID	NCT05257083
Type(s) de cancer	Myélome
Phase	Phase III
Type étude	Clinique
Médicament	Daratumumab, bortézomib, lénalidomide et Dexaméthasone (DVRd) suivi de Ciltacabtagène Autoleucel versus Daratumumab, bortézomib, lénalidomide et dexaméthasone (DVRd) suivi d'une greffe autologue de cellules souches
Institution	CHU DE QUEBEC – UNIVERSITE LAVAL HOPITAL DE L'ENFANT-JESUS 1401 18e Rue, Québec, QC, G1J 1Z4
Ville	Québec
Investigateur(trice) principal(e)	Dr Marc Lalancette
Coordonnateur(trice)	Philippe Nadeau 418-649-0252 poste 63115
Statut	Actif en recrutement
Date d'activation	01-08-2024
Critètes d'éligibilité	Participants with documented NDMM according to IMWG diagnostic criteria, for whom high-dose therapy and ASCT are part of the intended initial treatment plan. Measurable disease, as assessed by central laboratory, at screening as defined by any of the following: Serum monoclonal paraprotein (M-protein) level ≥1.0 g/dL or urine M-protein level ≥200 mg/24 hours; or Light chain MM without measurable disease in serum or urine: serum Ig free-light chain (FLC) ≥10 mg/dL and abnormal serum Ig kappa lambda FLC ratio. ECOG performance status of grade 0 or 1 Clinical laboratory values within prespecified range.
Critètes d'exclusion	Prior treatment with CAR-T therapy directed at any target. Any prior BCMA target therapy. Any prior therapy for MM or smoldering myeloma other than a short course of corticosteroids Received a strong cytochrome P450 (CYP)3A4 inducer within 5 half-lives prior to randomization Received or plans to receive any live, attenuated vaccine (except for COVID-19 vaccines) within 4 weeks prior to randomization. Known active, or prior history of central nervous system (CNS) involvement or clinical signs of meningeal involvement of MM Stroke or seizure within 6 months of signing Informed Consent Form (ICF)

Groupe d'étude en oncologie du Québec