Literature DB >> 30740733

Results from a 78-week, single-arm, open-label phase 2 study to evaluate UX007 in pediatric and adult patients with severe long-chain fatty acid oxidation disorders (LC-FAOD).

Jerry Vockley1,2, Barbara Burton3, Gerard T Berry4, Nicola Longo5, John Phillips6, Amarilis Sanchez-Valle7, Pranoot Tanpaiboon8, Stephanie Grunewald9, Elaine Murphy10, Alexandra Bowden11, Wencong Chen11, Chao-Yin Chen11, Jason Cataldo11, Deborah Marsden11, Emil Kakkis11.   

Abstract

Long-chain fatty acid oxidation disorders (LC-FAOD) are rare disorders characterized by acute crises of energy metabolism and severe energy deficiency that may present with cardiomyopathy, hypoglycemia, and/or rhabdomyolysis, which can lead to frequent hospitalizations and early death. An open-label Phase 2 study evaluated the efficacy of UX007, an investigational odd-carbon medium-chain triglyceride, in 29 subjects with severe LC-FAOD. UX007 was administered over 78 weeks at a target dose of 25-35% total daily caloric intake (mean 27.5%). The frequency and duration of major clinical events (hospitalizations, emergency room visits, and emergency home interventions due to rhabdomyolysis, hypoglycemia, and cardiomyopathy) occurring during 78 weeks of UX007 treatment was compared with the frequency and duration of events captured retrospectively from medical records for 78 weeks before UX007 initiation. The mean annualized event rates decreased from 1.69 to 0.88 events/year following UX007 initiation (p = 0.021; 48.1% reduction). The mean annualized duration rate decreased from 5.96 to 2.96 days/year (p = 0.028; 50.3% reduction). Hospitalizations due to rhabdomyolysis, the most common event, decreased from 1.03 to 0.63 events/year (p = 0.104; 38.7% reduction). Initiation of UX007 eliminated hypoglycemia events leading to hospitalization (from 11 pre-UX007 hospitalizations, 0.30 events/year vs. 0; p = 0.067) and intensive care unit (ICU) care (from 2 pre-UX007 ICU admissions, 0.05 events/year vs. 0; p = 0.161) and reduced cardiomyopathy events (3 events vs. 1 event; 0.07 to 0.02 events/year; 69.7% decrease). The majority of treatment-related adverse events (AEs) were mild to moderate gastrointestinal symptoms, including diarrhea, vomiting, and abdominal or gastrointestinal pain, which can be managed with smaller, frequent doses mixed with food.
© 2018 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM.

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Year:  2019        PMID: 30740733      PMCID: PMC6348052          DOI: 10.1002/jimd.12038

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  13 in total

1.  Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop.

Authors:  U Spiekerkoetter; M Lindner; R Santer; M Grotzke; M R Baumgartner; H Boehles; A Das; C Haase; J B Hennermann; D Karall; H de Klerk; I Knerr; H G Koch; B Plecko; W Röschinger; K O Schwab; D Scheible; F A Wijburg; J Zschocke; E Mayatepek; U Wendel
Journal:  J Inherit Metab Dis       Date:  2009-04-28       Impact factor: 4.982

Review 2.  Long-term major clinical outcomes in patients with long chain fatty acid oxidation disorders before and after transition to triheptanoin treatment--A retrospective chart review.

Authors:  Jerry Vockley; Deborah Marsden; Elizabeth McCracken; Stephanie DeWard; Amanda Barone; Kristen Hsu; Emil Kakkis
Journal:  Mol Genet Metab       Date:  2015-06-18       Impact factor: 4.797

3.  UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24weeks of treatment.

Authors:  J Vockley; B Burton; G T Berry; N Longo; J Phillips; A Sanchez-Valle; P Tanpaiboon; S Grunewald; E Murphy; R Humphrey; J Mayhew; A Bowden; L Zhang; J Cataldo; D L Marsden; E Kakkis
Journal:  Mol Genet Metab       Date:  2017-02-07       Impact factor: 4.797

4.  Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders.

Authors:  J Vockley; J Charrow; J Ganesh; M Eswara; G A Diaz; E McCracken; R Conway; G M Enns; J Starr; R Wang; J E Abdenur; J Sanchez-de-Toledo; D L Marsden
Journal:  Mol Genet Metab       Date:  2016-08-27       Impact factor: 4.797

Review 5.  Anaplerotic diet therapy in inherited metabolic disease: therapeutic potential.

Authors:  Charles R Roe; Fanny Mochel
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

6.  Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profile.

Authors:  Lei Gu; Guo-Fang Zhang; Rajan S Kombu; Frederick Allen; Gerd Kutz; Wolf-Ulrich Brewer; Charles R Roe; Henri Brunengraber
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-11-10       Impact factor: 4.310

7.  Heptanoate as a neural fuel: energetic and neurotransmitter precursors in normal and glucose transporter I-deficient (G1D) brain.

Authors:  Isaac Marin-Valencia; Levi B Good; Qian Ma; Craig R Malloy; Juan M Pascual
Journal:  J Cereb Blood Flow Metab       Date:  2012-10-17       Impact factor: 6.200

8.  Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.

Authors:  U Spiekerkoetter; M Lindner; R Santer; M Grotzke; M R Baumgartner; H Boehles; A Das; C Haase; J B Hennermann; D Karall; H de Klerk; I Knerr; H G Koch; B Plecko; W Röschinger; K O Schwab; D Scheible; F A Wijburg; J Zschocke; E Mayatepek; U Wendel
Journal:  J Inherit Metab Dis       Date:  2009-04-29       Impact factor: 4.982

9.  Carnitine palmitoyltransferase II deficiency: successful anaplerotic diet therapy.

Authors:  C R Roe; B-Z Yang; H Brunengraber; D S Roe; M Wallace; B K Garritson
Journal:  Neurology       Date:  2008-07-22       Impact factor: 9.910

10.  Anaplerotic treatment of long-chain fat oxidation disorders with triheptanoin: Review of 15 years Experience.

Authors:  Charles R Roe; Henri Brunengraber
Journal:  Mol Genet Metab       Date:  2015-10-24       Impact factor: 4.797

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  18 in total

1.  Metabolic analysis reveals evidence for branched chain amino acid catabolism crosstalk and the potential for improved treatment of organic acidurias.

Authors:  Stephen McCalley; David Pirman; Michelle Clasquin; Kendall Johnson; Shengfang Jin; Jerry Vockley
Journal:  Mol Genet Metab       Date:  2019-05-21       Impact factor: 4.797

2.  AAV9 gene replacement therapy for respiratory insufficiency in very-long chain acyl-CoA dehydrogenase deficiency.

Authors:  Marina Zieger; Allison M Keeler; Terence R Flotte; Mai K ElMallah
Journal:  J Inherit Metab Dis       Date:  2019-05-03       Impact factor: 4.982

3.  Neonatal Long-Chain 3-Ketoacyl-CoA Thiolase deficiency: Clinical-biochemical phenotype, sodium-D,L-3-hydroxybutyrate treatment experience and cardiac evaluation using speckle echocardiography.

Authors:  Annemarijne R J Veenvliet; Mark R Garrelfs; Floris E A Udink Ten Cate; Sacha Ferdinandusse; Simone Denis; Sabine A Fuchs; Marit Schwantje; Rosa Geurtzen; Annemiek M J van Wegberg; Marleen C D G Huigen; Leo A J Kluijtmans; Ronald J A Wanders; Terry G J Derks; Lonneke de Boer; Riekelt H Houtkooper; Maaike C de Vries; Clara D M van Karnebeek
Journal:  Mol Genet Metab Rep       Date:  2022-05-04

4.  Medium branched chain fatty acids improve the profile of tricarboxylic acid cycle intermediates in mitochondrial fatty acid β-oxidation deficient cells: A comparative study.

Authors:  Anuradha Karunanidhi; Clinton Van't Land; Dhivyaa Rajasundaram; Mateus Grings; Jerry Vockley; Al-Walid Mohsen
Journal:  J Inherit Metab Dis       Date:  2022-02-02       Impact factor: 4.750

5.  Open-label long-term treatment of add-on triheptanoin in adults with drug-resistant epilepsy.

Authors:  Karin Borges; Neha Kaul; Jack Germaine; Catalina Carrasco-Pozo; Patrick Kwan; Terence J O'Brien
Journal:  Epilepsia Open       Date:  2020-04-12

6.  Randomized trial of add-on triheptanoin vs medium chain triglycerides in adults with refractory epilepsy.

Authors:  Karin Borges; Neha Kaul; Jack Germaine; Patrick Kwan; Terence J O'Brien
Journal:  Epilepsia Open       Date:  2019-02-22

Review 7.  Recent Advances in the Pathophysiology of Fatty Acid Oxidation Defects: Secondary Alterations of Bioenergetics and Mitochondrial Calcium Homeostasis Caused by the Accumulating Fatty Acids.

Authors:  Alexandre Umpierrez Amaral; Moacir Wajner
Journal:  Front Genet       Date:  2020-11-27       Impact factor: 4.599

8.  Complex patterns of inheritance, including synergistic heterozygosity, in inborn errors of metabolism: Implications for precision medicine driven diagnosis and treatment.

Authors:  Jerry Vockley; Steven F Dobrowolski; Georgianne L Arnold; Ruben Bonilla Guerrero; Terry G J Derks; David A Weinstein
Journal:  Mol Genet Metab       Date:  2019-07-19       Impact factor: 4.797

9.  Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD).

Authors:  Abbe N Vallejo; Henry J Mroczkowski; Joshua J Michel; Michael Woolford; Harry C Blair; Patricia Griffin; Elizabeth McCracken; Stephanie J Mihalik; Miguel Reyes-Mugica; Jerry Vockley
Journal:  Clin Transl Immunology       Date:  2021-06-27

Review 10.  Triheptanoin: First Approval.

Authors:  Matt Shirley
Journal:  Drugs       Date:  2020-10       Impact factor: 9.546

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