Phase 2B Efficacy/Safety of Ornithine Phenylacetate in Hospitalized Cirrhotic Patients With Hepatic Encephalopathy (STOP-HE)
Sponsor: |
Ocera Therapeutics Inc. |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAM9458 |
U.S. Govt. ID: |
NCT01966419 |
Contact: |
Theresa Lukose: 212-305-3839 / tt2103@columbia.edu |
The purpose of this study is to evaluate the efficacy of the drug OCR-002 for the treatment of an acute hepatic encephalopathy episode in cirrhotic patients requiring hospitalization. Subjects who have been recently hospitalized will potentially receive OCR-002 via infusion on top of their standard care for 5 days. Patients will be assessed 24-hours after their last infusion and will have a follow-up visit 14 days after the end of the study dug infusion.
This study is closed
Investigator
Robert Brown, MD, MPH
Have you been diagnosed with Cirrhosis? |
Yes |
No |
Have you had a recent episode of Hepatic Encephalopathy? |
Yes |
No |
Have you been recently hospitalized with an acute episode of hepatic encephalopathy? |
Yes |
No |