Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study

Author:

De Giorgis Valentina1ORCID,Bhatia Kailash P.2,Boespflug‐Tanguy Odile3,Gras Domitille3,Marina Adela Della4ORCID,Desurkar Archana5,Toledo Manuel6,Miller Ian7,Rotstein Michael8,Schneider Susanne A.9ORCID,Tarquinio Daniel C.10,Weber Yvonne1112,Brandabur Melanie13,Mayhew Jill13,Koutsoukos Tony13,De Vivo Darryl C.14

Affiliation:

1. Department of Child Neurology and Psychiatry Mondino Foundation Pavia Italy

2. Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square London United Kingdom

3. Service de Neurologie Pédiatrique, Centre de Référence Leucodystrophies et Leucoencephalopathies de Cause Rare (LEUKOFRANCE), APHP Robert‐Debré Paris France

4. Department of Pediatric Neurology Centre for Neuromuscular Disorders, Centre for Translational Neuro‐ and Behavioral Sciences, University Hospital Essen, University Duisburg‐Essen Essen Germany

5. Neurology Department Sheffield Children's National Health Service Foundation Trust Sheffield United Kingdom

6. Epilepsy Unit, Neurology Department Hospital Vall d'Hebron Barcelona Spain

7. Department of Neurology and Comprehensive Epilepsy Program Brain Institute, Miami Children's Hospital Miami Florida USA

8. Pediatric Movement Disorders Service, The Pediatric Neurology Unite and Child Development Center, Tel Aviv Sourasky Medical Center Tel Aviv Israel

9. Department of Neurology Ludwig‐Maximilians‐University of München Munich Germany

10. Center for Rare Neurological Diseases Norcross Georgia USA

11. Department of Neurology and Epileptology Hertie Institute for Clinical Brain Research, University of Tübingen Tübingen Germany

12. Section of Epileptology, Department of Neurology University Hospital RWTH Aachen Aachen Germany

13. Ultragenyx Pharmaceutical Inc. Novato California USA

14. Department of Neurology and Pediatrics Columbia University New York New York USA

Abstract

AbstractBackgroundParoxysmal movement disorders are common in Glut1 deficiency syndrome (Glut1DS). Not all patients respond to or tolerate ketogenic diets.ObjectivesThe objective was to evaluate the effectiveness and safety of triheptanoin in reducing the frequency of disabling movement disorders in patients with Glut1DS not receiving a ketogenic diet.MethodsUX007G‐CL301 was a randomized, double‐blind, placebo‐controlled, phase 3 crossover study. After a 6‐week run‐in, eligible patients were randomized 1:1 to the first sequence (triheptanoin/placebo or placebo/triheptanoin) titration plus maintenance, followed by washout and the opposite sequence titration plus maintenance. The placebo (safflower oil) matched the appearance, taste, and smell of triheptanoin. Open‐label triheptanoin was administered in the extension. The frequency of disabling paroxysmal movement disorder events per 4 weeks (recorded by diary during maintenance; primary endpoint) was assessed by Wilcoxon rank‐sum test.ResultsForty‐three patients (children, n = 16; adults, n = 27) were randomized and treated. There was no difference between triheptanoin and placebo in the mean (interquartile range) number of disabling paroxysmal movement disorder events (14.3 [4.7–38.3] vs. 11.8; [3.2–28.7]; Hodges‐Lehmann estimated median difference: 1.46; 95% confidence interval, −1.12 to 4.36; P = 0.2684). Treatment‐emergent adverse events were mild/moderate in severity and included diarrhea, vomiting, upper abdominal pain, headache, and nausea. Two patients discontinued the study because of non‐serious adverse events that were predominantly gastrointestinal. The study was closed early during the open‐label extension because of lack of effectiveness. Seven patients continued to receive triheptanoin compassionately.ConclusionThere were no significant differences between the triheptanoin and placebo groups in the frequency of disabling movement disorder events during the double‐blind maintenance period. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Ultragenyx Pharmaceutical

Publisher

Wiley

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