Phase 2B Efficacy/Safety of Ornithine Phenylacetate in Hospitalized Cirrhotic Patients With Hepatic Encephalopathy (STOP-HE)
Study for treating patients with Hepatic Encephalopathy using drug, OCR-002
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
Additional Study Information: 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
Do You Qualify?
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
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For more information, please contact:
Theresa Lukose
tt2103@columbia.edu
212-305-3839