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Trial registered on ANZCTR


Registration number
ACTRN12618000970246
Ethics application status
Approved
Date submitted
4/06/2018
Date registered
8/06/2018
Date last updated
25/04/2024
Date data sharing statement initially provided
1/10/2019
Date results provided
25/04/2024
Type of registration
Prospectively registered

Titles & IDs
Public title
A safety and efficacy study of ATL1102 in patients with Duchenne Muscular Dystrophy
Scientific title
A Phase 2 open label, study to determine the safety, efficacy and pharmacokinetic profile of weekly dosing of ATL1102 in patients with non-ambulatory Duchenne Muscular Dystrophy.
Secondary ID [1] 294185 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Duchenne Muscular Dystrophy 306822 0
Condition category
Condition code
Human Genetics and Inherited Disorders 305928 305928 0 0
Other human genetics and inherited disorders
Musculoskeletal 307228 307228 0 0
Other muscular and skeletal disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
One cohort will be investigated. ATL1102 25mg/week, administered SC once weekly for 24 weeks in 25kg-65kg patients, (0.4-1mg/kg/w dose).
All doses of ATL1102 will be administered subcutaneously by a nurse in the hospital and by a nurse at home.
Monitoring of adherence to the intervention is by diary card and by return of the used and unused vials of investigational product and reconciliation at the hospital.
Intervention code [1] 300482 0
Treatment: Drugs
Comparator / control treatment
No control group.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 304960 0
Safety and tolerability as assessed by safety data on adverse events, injection site reactions and laboratory assessments.
Mild injection site erythema, increased liver enzymes and decreased platelet count.
These will be assessed visually and by biochemistry (bilirubin & gamma glutamyl transferase) and haematology respectively.
Timepoint [1] 304960 0
Assessed at screening, baseline (week 1, day 1) and during treatment weeks 1, 3, 5, 7, 8, 10, 12, 14, 16, 18, 20, 22, 24, and post treatment weeks 28 and 32.
Secondary outcome [1] 343743 0
Lymphocyte modulation assessed by haematological parameters lymphocytes, CD4 and CD8 T cells
Timepoint [1] 343743 0
Assessed at baseline, (week 1, day 1), and during treatment weeks 5, 8, 12, 24 and post treatment at week 28.
Secondary outcome [2] 347820 0
Performance of upper limb assessment will be assessed via the Myo-Pinch device (pinch strength),
Timepoint [2] 347820 0
Assessed at baseline (week 1, day 1) and during treatment weeks 5, 8, 12, and 24.
Secondary outcome [3] 347821 0
Performance of upper limb assessment will be assessed via the Myo-Grip device (grip strength).
Timepoint [3] 347821 0
Assessed at baseline (week 1, day 1) and during treatment weeks 5, 8, 12, and 24.
Secondary outcome [4] 375371 0
Performance of upper limb assessment will be assessed via the score as determined by the MoviPlate device (hand function) scores.
Timepoint [4] 375371 0
Assessed at baseline (week 1, day 1) and during treatment weeks 5, 8, 12, and 24.

Eligibility
Key inclusion criteria
Adolescent males aged 10 to 18 years with a diagnosis of non-ambulatory Duchenne Muscular Dystrophy for at least 3 months.
Minimum age
10 Years
Maximum age
18 Years
Sex
Males
Can healthy volunteers participate?
No
Key exclusion criteria
Ambulatory patients with DMD who are able to complete at least 75 meters during a 6-minute walk test, or have abnormal haematology values or a history of bleeding or coagulation abnormalities.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 2
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
A clinically important reduction in lymphocyte count from baseline to end of treatment was judged to be 25%, equating to a reduction of 0.47 (=0.75x1.89 x109/L) in mean lymphocyte count. A level of significance was set to 0.05 with a 2-sided paired t-test, resulting in a sample size of at least 9 participants being required to achieve a power of 80%.
Quantitative safety, efficacy, PK and PD data will be summarised by descriptive statistics (arithmetic mean, SD, SEM, median, minimum, and maximum) for both cohorts as well as overall and over time. Summaries will be presented for the change from baseline, when appropriate. Qualitative variables will be summarised by frequency, percentage of patients, and Clopper-Pearson 95% CI for the cohort, overall ,and over time. For key efficacy variables, the paired t-test will be used to test the change from baseline to end of treatment.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
2/07/2018
Actual
28/08/2018
Date of last participant enrolment
Anticipated
22/10/2018
Actual
27/05/2019
Date of last data collection
Anticipated
31/12/2019
Actual
25/03/2020
Sample size
Target
9
Accrual to date
Final
9
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 10231 0
The Royal Childrens Hospital - Parkville
Recruitment postcode(s) [1] 21895 0
3052 - Parkville

Funding & Sponsors
Funding source category [1] 298819 0
Commercial sector/Industry
Name [1] 298819 0
Antisense Therapeutics Limited
Country [1] 298819 0
Australia
Primary sponsor type
Commercial sector/Industry
Name
Antisense Therapeutics Limited
Address
6 Wallace Avenue
Toorak, Victoria, 3142
Country
Australia
Secondary sponsor category [1] 298015 0
None
Name [1] 298015 0
Address [1] 298015 0
Country [1] 298015 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 299768 0
The Royal Children's Hospital Human Research Ethics Committee
Ethics committee address [1] 299768 0
Ethics committee country [1] 299768 0
Australia
Date submitted for ethics approval [1] 299768 0
10/01/2018
Approval date [1] 299768 0
21/05/2018
Ethics approval number [1] 299768 0
HREC37114C

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 81502 0
Dr Ian Woodcock
Address 81502 0
The Royal Children's Hospital
50 Flemington Road
Parkville, Vic 3052
Country 81502 0
Australia
Phone 81502 0
+61 3 9345 5661
Fax 81502 0
Email 81502 0
Ian.Woodcock@rch.org.au
Contact person for public queries
Name 81503 0
Susan Turner
Address 81503 0
Percheron Therapeutics Limited
Level 30. 35 Collins Street
ME.LBOURNE VIC 3000
Country 81503 0
Australia
Phone 81503 0
+61 398278999
Fax 81503 0
Email 81503 0
info@percherontx.com
Contact person for scientific queries
Name 81504 0
Ian Woodcock
Address 81504 0
The Royal Children's Hospital
50 Flemington Road
Parkville, Vic 3052
Country 81504 0
Australia
Phone 81504 0
+61 3 9345 5661
Fax 81504 0
Email 81504 0
Ian.Woodcock@rch.org.au

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
Privacy and intellectual property considerations


What supporting documents are/will be available?

No Supporting Document Provided


Results publications and other study-related documents

Documents added manually
TypeIs Peer Reviewed?DOICitations or Other DetailsAttachment
Study results articleYes Woodcock IR, Tachas G, Desem N, Houweling PJ, Kean... [More Details]

Documents added automatically
SourceTitleYear of PublicationDOI
Dimensions AIVLA-4 Expression and Activation in B Cell Malignancies: Functional and Clinical Aspects2020https://doi.org/10.3390/ijms21062206
EmbaseCardiorespiratory management of Duchenne muscular dystrophy: emerging therapies, neuromuscular genetics, and new clinical challenges.2022https://dx.doi.org/10.1016/S2213-2600%2821%2900581-6
EmbaseEmerging therapies for Duchenne muscular dystrophy.2022https://dx.doi.org/10.1016/S1474-4422%2822%2900125-9
EmbaseTherapeutic approaches to preserve the musculature in Duchenne Muscular Dystrophy: The importance of the secondary therapies.2022https://dx.doi.org/10.1016/j.yexcr.2021.112968
Dimensions AITargeting integrins in drug-resistant acute myeloid leukaemia2023https://doi.org/10.1111/bph.16149
EmbaseA phase 2 open-label study of the safety and efficacy of weekly dosing of ATL1102 in patients with non-ambulatory Duchenne muscular dystrophy and pharmacology in mdx mice.2024https://dx.doi.org/10.1371/journal.pone.0294847
N.B. These documents automatically identified may not have been verified by the study sponsor.