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Title
Status

 

M13-833 - A Study of the Safety and Pharmacokinetics of Venetoclax in Pediatric and Young Adult Patients With Relapsed or Refractory Malignancies

Closed

M13-833 - A Study of the Safety and Pharmacokinetics of Venetoclax in Pediatric and Young Adult Patients With Relapsed or Refractory Malignancies

Go to Health Care Provider version

DiagnosisALL AML all solid tumoursStudy StatusClosed
PhaseI
AgeChild, Adult - (Up to 25 years)RandomisationNO
Line of treatmentDisease relapse or progression
Routes of Treatment AdministrationOral tablet or suspension (Venetoclax) IV Chemotherapies
Last Posted Update2024-03-18
ClinicalTrials.gov #NCT03236857
International Sponsor
AbbVie
Principal Investigators for Canadian Sites
The Hospital for Sick Children – Dr. Daniel Morgenstern
CHU Ste-Justine- Dr. Henrique Bittencourt
Centres
Medical contact

Dr. Daniel Morgenstern

daniel.morgenstern@sickkids.ca

Social worker/patient navigator contact

Karen Fung 

karen.fung@sickkids.ca

Clinical research contact

New Agent and Innovative Therapies (NAIT) 

nait.info@sickkids.ca

 

Medical contact
Dr. Henrique Bittencourt
Dr. Monia Marzouki
Dr. Sebastien Perreault (neuro-onc)
 
Social worker/patient navigator contact
Marie-Claude Charrette
 
Clinical research contact
Marie Saint-Jacques
 

 

 

Study Description

Venetoclax is a medication, taken by mouth, which selectively binds and blocks a molecule called BCL-2, restoring the ability for natural cell death in cancer cells that have the BCL-2 marker. It is expected to slow or stop the growth of cancer cells.

The aim of this study is to evaluate the dose, safety, tolerability, antitumor activity and other characteristics of venetoclax given with or without chemotherapy.

Inclusion Criteria
  • Participants must have cancer that has come back or is not responding to current therapy
  • Age up to 25 years
  • Multiple other inclusion and exclusion criteria could apply and will be reviewed by your treating team.