Emergency Use of OCR-002 in Acute Liver Failure (ALF)

NCT01634230 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2021-06-24

No results posted yet for this study

Summary

This study provides emergency use of the unapproved study medication in ALF patients with acute liver failure who are not responding to standard of care.

Conditions

  • Acute Liver Failure

Interventions

DRUG

OCR-002

daily dose: 10 g infused over 24 hours

Sponsors & Collaborators

  • Ocera Therapeutics, Inc.

    lead INDUSTRY

Principal Investigators

  • Global Clinical Leader · Ocera Therapeutics

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

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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 NCT01634230 on ClinicalTrials.gov