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Clinical trialNCT00107770CompletedPhase 1/PHASE2Interventional

Safety Study of Oral Sodium Phenylbutyrate in Subjects With ALS (Amyotrophic Lateral Sclerosis)

SponsorUS Department of Veterans AffairsEnrollment40Amyotrophic Lateral Sclerosis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of the study is to evaluate the safety of sodium phenylbutyrate (NaPB) treatment in subjects with amyotrophic lateral sclerosis (ALS) and the ability to take this medication without major side effects.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Robert Ferrante, PhD MSc

    Edith Nourse Rogers Memorial Veterans Hospital, Bedford

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

10 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Va Medical Center, Iowa City

    Iowa City, Iowa, United States

  • Va Medical Center, Lexington

    Lexington, Kentucky, United States

  • Va Maryland Health Care System, Baltimore

    Baltimore, Maryland, United States

  • Edith Nourse Rogers Memorial Veterans Hospital, Bedford

    Bedford, Massachusetts, United States

  • Va Medical Center, Jamaica Plain Campus

    Boston, Massachusetts, United States

  • Va Medical Center, Syracuse

    Syracuse, New York, United States

  • Va Medical Center, Durham

    Durham, North Carolina, United States

  • Va Medical Center, Cincinnati

    Cincinnati, Ohio, United States

  • Va Pittsburgh Health Care System

    Pittsburgh, Pennsylvania, United States

  • Michael E. Debakey Va Medical Center (152)

    Houston, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Apr 2005
Primary completion
30 Nov 2006
Completion
30 Sept 2007
Last update posted
11 Jan 2010
Registered enrollment
40
Registry id
NCT00107770

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.