An Intermediate Size Expanded Access Protocol of AMX0035 for ALS

NCT05286372 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2022-10-18

No results posted yet for this study

Summary

The Expanded Access Program will provide access and assess the safety of AMX0035 for the treatment of people living with ALS.

Conditions

Interventions

DRUG

AMX0035

Proprietary formulation of sodium phenylbutyrate and taurursodiol

Sponsors & Collaborators

  • Amylyx Pharmaceuticals Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States
  • Puerto Rico

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05286372 on ClinicalTrials.gov