Effect of Nilotinib in Cerebellar Ataxia Patients
Primary Purpose
Ataxia, Cerebellar, Ataxia, Progressive
Status
Completed
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Nilotinib
Sponsored by
About this trial
This is an interventional treatment trial for Ataxia, Cerebellar focused on measuring spinocerebellar ataxia, treatment, nilotinib, bcr-abl, receptor-tyrosine-kinase-inhibitor
Eligibility Criteria
Inclusion Criteria:
- Diagnosed as chronic cerebellar ataxia
- Confirmed as spinocerebellar ataxia by gene test
Exclusion Criteria:
- Laboratory abnormalities that could interfere with the proper use of Nilotinib QTc interval >450ms on initial electrocardiograph, Hb <8.0, WBC<2000, ANC <1600, PLT <140,000, AST >200, ALT>200, ALP>575, Positive HIV serology, active hepatitis B
- Unstable mental or physical status that could interfere with precise evaluation and proper management of SCA Heart failure (NYHA Grade III or IV), history of major heart disease Pregnancy, on breast feeding
Sites / Locations
- Seoul National University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Nilotinib group
Arm Description
Patients with SCA and taking nilotinib treatment
Outcomes
Primary Outcome Measures
Activity of daily living
Barthel index: score range 0-6
Secondary Outcome Measures
Cerebellar function
Scale for the assessment and rating of ataxia (SARA): score range 0-36
General function
Rating scale for Friedreich's ataxia I: score range 0-6
Activity of daily living
Rating scale for Friedreich's ataxia II: score range 0-36
Full Information
NCT ID
NCT03932669
First Posted
April 25, 2019
Last Updated
September 23, 2021
Sponsor
Seoul National University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03932669
Brief Title
Effect of Nilotinib in Cerebellar Ataxia Patients
Official Title
Effect of Nilotinib in Cerebellar Ataxia Patients
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
November 19, 2018 (Actual)
Primary Completion Date
August 13, 2020 (Actual)
Study Completion Date
August 13, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is an institutional cohort study. Patients confirmed with spinocerebellar ataxia (SCA) and taking or planning to take Nilotinib (Tasigna®) are enrolled in this study. The daily dose of Nilotinib is 150mg-300mg and the patients will be followed up at 1, 3, 6, and 12 months. Rating scale for Friedreich's ataxia I and II and Barthel index are used as general function and daily living performance index. Scale for assessment and rating of ataxia (SARA) are used as an objective measure of cerebellar function. Adverse drug reactions are evaluated based on CTCAE version 4.0.
Detailed Description
Patients taking Nilotinib 1-1.Baseline information: demographics, genetic type of SCA, brain MRI, electrocardiography, routine blood evaluations 1-2. Time point of evaluation: At initiation of taking Nilotinib, 1, 3, 6, and 12 months 1-3. Evaluation items (at each time point) Routine check-up: electrocardiography, routine blood evaluations Adverse events: CTCAE version 4.0 Daily living performance: Barthel index General function: Friedreich's ataxia I and II 1-4. Change of drug dose Based on the attending physician's decision
Patients planning to take Nilotinib 2-1.Baseline information: demographics, genetic type of SCA, brain MRI, electrocardiography, routine blood evaluations 2-2. Time point of evaluation: Baseline, 1, 3, 6, and 12 months 2-3. Evaluation items (at each time point) Routine check-up: electrocardiography, routine blood evaluations Adverse events: CTCAE version 4.0 Cerebellar function: Scale for assessment and rating of ataxia (SARA) Daily living performance: Barthel index General function: Friedreich's ataxia I and II 2-4. Change of drug dose Based on the attending physician's decision
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ataxia, Cerebellar, Ataxia, Progressive
Keywords
spinocerebellar ataxia, treatment, nilotinib, bcr-abl, receptor-tyrosine-kinase-inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
70 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nilotinib group
Arm Type
Experimental
Arm Description
Patients with SCA and taking nilotinib treatment
Intervention Type
Drug
Intervention Name(s)
Nilotinib
Intervention Description
150-300mg daily dose of nilotinib
Primary Outcome Measure Information:
Title
Activity of daily living
Description
Barthel index: score range 0-6
Time Frame
12 month
Secondary Outcome Measure Information:
Title
Cerebellar function
Description
Scale for the assessment and rating of ataxia (SARA): score range 0-36
Time Frame
12 month
Title
General function
Description
Rating scale for Friedreich's ataxia I: score range 0-6
Time Frame
12 month
Title
Activity of daily living
Description
Rating scale for Friedreich's ataxia II: score range 0-36
Time Frame
12 month
Other Pre-specified Outcome Measures:
Title
Occurrence of adverse events
Description
CTCAE version 4.0
Time Frame
Baseline, 1 month, 3 month, 6 month, 12 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed as chronic cerebellar ataxia
Confirmed as spinocerebellar ataxia by gene test
Exclusion Criteria:
Laboratory abnormalities that could interfere with the proper use of Nilotinib QTc interval >450ms on initial electrocardiograph, Hb <8.0, WBC<2000, ANC <1600, PLT <140,000, AST >200, ALT>200, ALP>575, Positive HIV serology, active hepatitis B
Unstable mental or physical status that could interfere with precise evaluation and proper management of SCA Heart failure (NYHA Grade III or IV), history of major heart disease Pregnancy, on breast feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kon Chu, MD, PhD
Organizational Affiliation
Seoul National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
03080
Country
Korea, Republic of
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
The IPD will be provided upon request from any qualified investigator.
Citations:
PubMed Identifier
28601294
Citation
Lee WJ, Moon J, Kim TJ, Jun JS, Lee HS, Ryu YJ, Lee ST, Jung KH, Park KI, Jung KY, Kim M, Lee SK, Chu K. The c-Abl inhibitor, nilotinib, as a potential therapeutic agent for chronic cerebellar ataxia. J Neuroimmunol. 2017 Aug 15;309:82-87. doi: 10.1016/j.jneuroim.2017.05.015. Epub 2017 May 24.
Results Reference
result
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Effect of Nilotinib in Cerebellar Ataxia Patients
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