Evidence map›Paper›PMID 32885845›Full record

Trial reportJournal of inherited metabolic disease2021

Effects of triheptanoin (UX007) in patients with long-chain fatty acid oxidation disorders: Results from an open-label, long-term extension study.

Jerry Vockley, Barbara Burton, Gerard Berry, Nicola Longo, John Phillips, Amarilis Sanchez-Valle, Kimberly Chapman, Pranoot Tanpaiboon, Stephanie Grunewald, Elaine Murphy and 2 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Journal of inherited metabolic disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02214160 (An Open-label Long-Term Safety and Efficacy Extension Study in Subjects With Long-Chain Fatty Acid Oxidation Disorders), which is not on this map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02214160 phase2completednot on this map

An Open-label Long-Term Safety and Efficacy Extension Study in Subjects With Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) Previously Enrolled in UX007 or Triheptanoin Studies

TypeinterventionalSponsorUltragenyx Pharmaceutical IncRan2014 to 2020Enrolled94ConditionsCarnitine Palmitoyltransferase (CPT I or CPT II) Deficiency, Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Long-chain 3-hydroxy-acyl-CoA Dehydrogenase (LCHAD) Deficiency, Trifunctional Protein (TFP) DeficiencyArmsUX007
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Guideline
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  13. Review
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  16. The Physiological and Pathological Role of Acyl-CoA Oxidation.International journal of molecular sciences · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 10 institutions in 2 countries.

Jerry VockleyUniversity of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-8180-6457
Barbara BurtonAnn & Robert H. Lurie Children's Hospital, Chicago, Illinois, USA.
Gerard BerryBoston Children's Hospital, Boston, Massachusetts, USA.
Nicola LongoUniversity of Utah, Salt Lake City, Utah, USA.
John PhillipsVanderbilt University Medical Center, Nashville, Tennessee, USA.
Amarilis Sanchez-ValleUSF Health, Morsani College of Medicine, Tampa, Florida, USA.
Kimberly ChapmanChildren's National Health System, Washington, District of Columbia, USA.
Pranoot TanpaiboonChildren's National Health System, Washington, District of Columbia, USA.
Stephanie GrunewaldGreat Ormond Street Hospital and Institute of Child Health, NIHR Biomedical Research Center (BRC), UCL, London, UK.
Elaine MurphyNational Hospital for Neurology and Neurosurgery, London, UK.
Xiaoxiao LuUltragenyx Pharmaceutical Inc., Novato, California, USA.
Jason CataldoUltragenyx Pharmaceutical Inc., Novato, California, USA.
Children's National · USUltragenyx Pharmaceutical (United States) · USBoston Children's Hospital · USGreat Ormond Street Hospital · GBLurie Children's Hospital · USNational Hospital for Neurology and Neurosurgery · GBUniversity of Pittsburgh · USUniversity of South Florida · USUniversity of Utah · USVanderbilt University Medical Center · US

Funding

Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
Inborn Errors of Long Chain Fat MetabolismR01DK078775 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VOCKLEY, GERARD · 2008 to 2019
$4.5M
NCATS NIH HHS UL1 TR002538NIDDK NIH HHS R01 DK078775
6 · The paper itself

Abstract

Long-chain fatty acid oxidation disorders (LC-FAOD) are autosomal recessive conditions that impair conversion of long-chain fatty acids into energy, leading to significant clinical symptoms. Triheptanoin is a highly purified, 7-carbon chain triglyceride approved in the United States as a source of calories and fatty acids for treatment of pediatric and adult patients with molecularly confirmed LC-FAOD. CL202 is an open-label, long-term extension study evaluating triheptanoin (Dojolvi) safety and efficacy in patients with LC-FAOD. Patients rolled over from the CL201 triheptanoin clinical trial (rollover); were triheptanoin-naïve (naïve); or had participated in investigator-sponsored trials/expanded access programs (IST/other). Results focus on rollover and naïve groups, as pretreatment data allow comparison. Primary outcomes were annual rate and duration of major clinical events (MCEs; rhabdomyolysis, hypoglycemia, and cardiomyopathy events). Seventy-five patients were enrolled (24 rollover, 20 naïve, 31 IST/other). Mean study duration was 23.0 months for rollover, 15.7 months for naïve, and 34.7 months for IST/other. In the rollover group, mean annualized MCE rate decreased from 1.76 events/year pre-triheptanoin to 0.96 events/year with triheptanoin (P = .0319). Median MCE duration was reduced by 66%. In the naïve group, median annualized MCE rate decreased from 2.33 events/year pre-triheptanoin to 0.71 events/year with triheptanoin (P = .1072). Median MCE duration was reduced by 80%. The most common related adverse events (AEs) were diarrhea, abdominal pain/discomfort, and vomiting, most mild to moderate. Three patients had serious AEs (diverticulitis, ileus, rhabdomyolysis) possibly related to drug; all resolved. Two patients had AEs leading to death; neither drug related. Triheptanoin reduced rate and duration of MCEs. Safety was consistent with previous observations.

Indexed as

AdolescentAdultCardiomyopathiesChildChild, PreschoolFatty AcidsFemaleHumansHypoglycemiaInfantLipid Metabolism, Inborn ErrorsMaleMiddle AgedOxidation-ReductionRhabdomyolysisTriglyceridesFatty AcidsTriglyceridestriheptanoincardiomyopathylong-chain fatty acid oxidation disorders (LC-FAOD)rhabdomyolysistriheptanoin (UX007)

Identifiers

PMID32885845
PMCPMC7891391
OpenAlexW3083075215

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.