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Iron Chelator
Deferasirox plus amlodipine for Iron Overload (CANALI Trial)
N/A
Waitlist Available
Led By Kevin HM Kuo, MD MSc FRCPC
Research Sponsored by Kevin H.M. Kuo, MD, MSc, FRCPC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months following randomization
Awards & highlights
CANALI Trial Summary
This is a randomized, open label, two arms superiority trial of a representative population of patients with a primary diagnosis of transfusion dependent thalassemia with evidence of moderate cardiac iron overload, defined as an average T2* MRI parameter at the mid inter-ventricular septum between 10 and 20ms.
Eligible Conditions
- Iron Overload
- Beta Thalassemia
CANALI Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months following randomization
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months following randomization
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in cardiac T2*
Secondary outcome measures
Change in left ventricular ejection fraction
Number of Participants with Adverse Events
CANALI Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Deferasirox plus amlodipineExperimental Treatment2 Interventions
deferasirox iron chelation therapy with amlodipine
Group II: DeferasiroxActive Control1 Intervention
deferasirox iron chelation therapy and standard of care by the treating physician
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Amlodipine
FDA approved
Deferasirox
FDA approved
Find a Location
Who is running the clinical trial?
Kevin H.M. Kuo, MD, MSc, FRCPCLead Sponsor
1 Previous Clinical Trials
50 Total Patients Enrolled
Kevin HM Kuo, MD MSc FRCPCPrincipal InvestigatorUniversity Health Network, Toronto
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