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Clinical Trials/NCT05938023
NCT05938023
Terminated
Phase 2

A Multicentre, Randomised, Double-blind, Placebo-controlled and Open Label Extension Study to Assess the Efficacy, Safety, and Pharmacokinetic Profile of of ATL1102 in Non-ambulatory Participants with Duchenne Muscular Dystrophy

Percheron Therapeutics13 sites in 5 countries48 target enrollmentMay 18, 2023

Overview

Phase
Phase 2
Intervention
ATL1102 25mg
Conditions
Duchenne Muscular Dystrophy
Sponsor
Percheron Therapeutics
Enrollment
48
Locations
13
Primary Endpoint
Change in the Performance of Upper Limb (PUL) 2.0 score from baseline to Week 49 (combined treatment period).
Status
Terminated
Last Updated
last year

Overview

Brief Summary

This Phase IIb study is a two part, multicenter study to evaluate the efficacy, safety, pharmacokinetics and pharmacodynamics of ATL1102 in non-ambulant boys with Duchenne Muscular Dystrophy aged 10 to <18 years old. The study includes a randomised, double-blind, placebo-controlled treatment period (Part A), followed by an open labelled treatment period (Part B).

Detailed Description

This Phase IIb study is a two part, multicenter study to evaluate the efficacy, safety, pharmacokinetics and pharmacodynamics of ATL1102 and will enroll 45 non-ambulant boys with Duchenne Muscular Dystrophy (DMD) aged 10 to \<18 years old. During the 24 week randomised, double-blind, placebo-controlled treatment period (Part A) participants will be enrolled and randomised to receive either ATL1102 25mg, ATL1102 50mg or matched placebo in a 1:1:1 ratio given as a weekly subcutaneous injection. Participants will then continue to the 24 week Open Labelled Treatment Period (Part B) and continue to receive ATL1102 25mg or ATL1102 50mg for a further 24 weeks. Participants on placebo in Part A will transition to ATL1102. The study will consist of a 4 week screening period, 24 week randomised, double-blind, placebo-controlled treatment period (Part A), 24 week open label treatment period (Part B) and 16 week follow up period.

Registry
clinicaltrials.gov
Start Date
May 18, 2023
End Date
January 15, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
Percheron Therapeutics
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Has a clinical diagnosis of DMD confirmed by validated genetic testing
  • Is considered to be non-ambulatory, defined as unable to walk 10 meters without assistance or help at Screening.
  • Male aged 10 to less than 18 years, at the time of Screening.
  • Body weight of at least 25 kg at Screening.
  • If receiving corticosteroid therapy, therapy was initiated at least six months prior to the baseline visit and a stable daily dose for at least 3 months prior to baseline
  • Participant has a Performance of Upper Limb Module for DMD 2.0 (PUL 2.0) Entry Item A score ≥
  • Able to perform spirometry and has sufficient Respiratory function defined as reproducible percent predicted FVC ≥50%.
  • Has adequate cardiac function defined as left ventricular ejection fraction (LVEF) ≥45% by echocardiogram and if receiving cardiac medication, must be currently on a stable regimen and doses of cardiac therapy (at least 3 months prior to baseline Day 1)
  • Participant and their parent/guardian/carer are willing and able to comply with scheduled visits, study medication administration and study procedures.

Exclusion Criteria

  • Participation in another clinical trial (non-interventional) or administration of any investigational product or experimental product within 12 weeks or 5 half-lives (whichever is longer) preceding Day
  • Exposure to more than 3 investigational products within the 12 months prior to Day
  • History of clinically significant bleeding or coagulation abnormalities or clinically significant abnormal coagulation parameters.
  • Currently receiving antiplatelet or anticoagulant therapy or has taken medication with an antiplatelet or anticoagulant effect within 4 weeks prior Day 1
  • Any evidence of clinically significant structural or functional heart abnormality (cardiomyopathy that is managed by ACEi or beta blockers is acceptable provided the LVEF inclusion criterion is met).
  • Known history of or a positive test for hepatitis B surface antigen (HBsAg), hepatitis C (HCV) antibodies, human immunodeficiency virus (HIV) antibodies at Screening.
  • Evidence of renal impairment and/or cystatin C \>1.4 mg/L.
  • Received a live vaccine (including intranasal influenza vaccine) within 4 weeks prior to Day 1 or planned live vaccination during the study period.
  • Asthma (if requiring regular medication), bronchitis/chronic obstructive pulmonary disease (COPD), bronchiectasis, emphysema, pneumonia or the presence of any non-DMD respiratory illness that affects PEF and FVC or other respiratory measures.
  • Requires day-time assisted mechanical or non-invasive ventilation (NIV) (night time NIV is permitted).

Arms & Interventions

ATL1102 25mg

ATL1102 25mg administered subcutaneously once weekly

Intervention: ATL1102 25mg

ATL1102 50mg

ATL1102 50mg administered subcutaneously once weekly

Intervention: ATL1102 50mg

Placebo

Placebo is administered subcutaneously once weekly

Intervention: Placebo

Outcomes

Primary Outcomes

Change in the Performance of Upper Limb (PUL) 2.0 score from baseline to Week 49 (combined treatment period).

Time Frame: 49 weeks

The PUL is an assessment used to evaluate the upper limb strength for individuals with DMD where a higher score indicates a better outcome with a minimum of 0 and a maximum score of 42

Change in the Performance of Upper Limb (PUL) 2.0 score from baseline to Week 25 (blinded treatment period).

Time Frame: 25 weeks

The PUL is an assessment used to evaluate the upper limb strength for individuals with DMD where a higher score indicates a better outcome with a minimum of 0 and a maximum score of 42

Change in the Performance of Upper Limb (PUL) 2.0 score from Week 25 to Week 49 (open label treatment period).

Time Frame: 49 weeks

The PUL is an assessment used to evaluate the upper limb strength for individuals with DMD where a higher score indicates a better outcome with a minimum of 0 and a maximum score of 42

Safety measured by the incidence and frequency of adverse events, serious adverse events and suspected unexpected adverse events from baseline to Week 65

Time Frame: 65 weeks

An Adverse Event is any untoward medical occurrence in a participant and does not necessarily have to have a causal relationship with the intervention.

Secondary Outcomes

  • Change in the grip strength of the hand from baseline to Week 49 using a handheld dynamometer tool (MyoGrip) (combined treatment period).(49 weeks)
  • Change in the respiratory function assessed by peak expiratory flow (PEF) from baseline to Week 49 (combined treatment period).(49 weeks)
  • Change in the respiratory function assessed by Forced Vital Capacity (FVC) from baseline to Week 25 (blinded treatment period).(25 weeks)
  • Safety measured by the incidence and frequency of adverse events, serious adverse events and suspected unexpected adverse events from baseline to Week 25 (blinded treatment period).(25 weeks)
  • Time to Cmax and Cmin for ATL1102 over multiple timepoints(65 weeks)
  • The terminal half life for ATL1102(65 weeks)
  • Change in the grip strength of the hand from baseline to Week 25 using a handheld dynamometer tool (MyoGrip) (blinded treatment period).(25 weeks)
  • Change in the pinch strength of the fingers from Week 25 to Week 49 using handheld dynamometer tool (MyoPinch) (open label treatment period).(49 weeks)
  • Change in the respiratory function assessed by peak expiratory flow (PEF) from Week 25 to Week 49 (open label treatment period).(49 weeks)
  • Change in the Paediatric Quality of Life (PedsQL) questionnaire Duchenne Muscular Dystrophy (DMD) Module from Week 25 to Week 49 (open label treatment period).(49 weeks)
  • Change in the pinch strength of the fingers from Baseline to Week 49 using handheld dynamometer tool (MyoPinch) (combined treatment period).(49 weeks)
  • Change in the respiratory function assessed by Forced Vital Capacity (FVC) from Baseline to Week 49 (combined treatment period).(49 weeks)
  • Change in the Paediatric Quality of Life (PedsQL) questionnaire Duchenne Muscular Dystrophy (DMD) Module from Baseline to Week 49 (combined treatment period).(49 weeks)
  • Change in the pinch strength of the fingers from baseline to Week 25 using handheld dynamometer tool (MyoPinch) (blinded treatment period).(25 weeks)
  • Change in the respiratory function assessed by peak expiratory flow (PEF) from baseline to Week 25 (blinded treatment period).(25 weeks)
  • Change in the Paediatric Quality of Life (PedsQL™) questionnaire Duchenne Muscular Dystrophy (DMD) Module from baseline to Week 25 (blinded treatment period).(25 weeks)
  • Area under the plasma concentration time curve (AUC) for ATL1102 over multiple timepoints(65 weeks)
  • Maximum and minimum plasma concentration (Cmax and Cmin) for ATL1102 over multiple timepoints(65 weeks)
  • Change in the grip strength of the hand from Week 25 to Week 49 using a handheld dynamometer tool (MyoGrip) (open label treatment period).(49 weeks)
  • Change in the respiratory function assessed by Forced Vital Capacity (FVC) from Week 25 to Week 49 (open label treatment period).(49 weeks)

Study Sites (13)

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