CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 15 enrolled
Drug / intervention
Triheptanoindrug
Likely dose
Triheptanoin 1gfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03506425
NCT03506425Phase 2Completed

A Pilot Trial of Triheptanoin for People With Amyotrophic Lateral Sclerosis (PALS)

Richard Bedlack, M.D., Ph.D.·interventional·Posted Apr 24, 2018·Updated Dec 24, 2019

In Brief

A Phase 2 clinical trial evaluating Triheptanoin for ALS. Completed, enrolled 15 participants across 1 site.

Detailed Summary

The causes of ALS are largely unknown. However, mitochondrial dysfunction, resulting in impaired energy production, oxidative stress and apoptosis, may play a key role in ALS progression. Triheptanoin can improve mitochondrial function and energy production and therefore has potential for slowing ALS progression. Indeed, triheptanoin slowed motor neuron loss and delayed the onset of weakness in a mutant SOD1 model of ALS. This pilot trial will determine if Triheptanoin is safe tolerable, alters biomarkers of brain energy metabolism and oxidative stress, and slows functional decline in people with ALS.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsALS
CountriesUnited States

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedApr 24, 2018
Enrollment StartJun 21, 2018
Primary CompletionMar 28, 2019
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 8.2 years ago

Interventions

Triheptanoindrug

Triheptanoin is a medium chain triglyceride (MCT) that can improve mitochondrial function and energy production and therefore has potential for slowing ALS progression. Indeed, triheptanoin slowed motor neuron loss and delayed the onset of weakness in a mutant SOD1 model of ALS. The Triheptanoin we will use is a colorless to light yellow oil. The target triheptanoin dose for this study is 1g/kg/d. This target dose was selected because it was safe and tolerable and altered brain MR spectroscopy in patients with Huntington's Disease.