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D.08 ACT DMD (Ataluren Confirmatory Trial in Duchenne Muscular Dystrophy): effect of Ataluren on timed function tests (TFT) in nonsense mutation (nm) DMD

Published online by Cambridge University Press:  17 June 2016

N Goemans
Affiliation:
(Leuven)
C Campbell
Affiliation:
(London)
CM McDonald
Affiliation:
(Sacramento)
T Voit
Affiliation:
(London)
X Luo
Affiliation:
(South Plainfield)
G Elfring
Affiliation:
(South Plainfield)
H Kroger
Affiliation:
(South Plainfield)
P Riebling
Affiliation:
(South Plainfield)
T Ong
Affiliation:
(South Plainfield)
R Spiegel
Affiliation:
(South Plainfield)
SW Peltz
Affiliation:
(South Plainfield)
K Bushby
Affiliation:
(Newcastle upon Tyne)
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Abstract

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Background: Ataluren is the first drug to treat the underlying cause of nmDMD. Methods: ACT DMD is a Phase 3, randomized, double-blind study. Males 7-16 years with nmDMD and a screening six-minute walk distance (6MWD) ≥150 m and <80%-predicted were randomized to ataluren 40 mg/kg/day or placebo for 48 weeks. A pre-specified subgroup included patients with baseline 6MWD 300-400 m. A meta-analysis of the overall ACT DMD population and the ‘ambulatory decline phase’ subgroup of the Phase 2b study (those patients meeting ACT DMD entry criteria) was pre-specified in the statistical plan. Results: In the overall ACT DMD population (N=228), changes in TFTs favored ataluren over placebo: 10-meter walk/run, -1.2s (p=0.117); 4-stair climb, -1.8s (p=0.058); 4-stair descend, -1.8s (p=0.012). In the pre-specified subgroup (n=99), these differences increased to -2.1s, -3.6s, and -4.3s, respectively, and were statistically significant (p<0.01) for 4-stair climb and descend. Results are supported by the meta-analysis (N=291), which demonstrated significant differences (p<0.05) in 10-meter walk/run, 4-stair climb, 4-stair descend. Conclusions: TFT results showed a benefit for ataluren in ACT DMD, and a larger treatment effect in the pre-specified baseline 6MWD 300-400 m subgroup as well as the pre-specified meta-analysis of ACT DMD and the Phase 2b study decline subgroup.

Supported By: PTC Therapeutics Inc.

Type
Platform Presentations
Copyright
Copyright © The Canadian Journal of Neurological Sciences Inc. 2016