A Randomized, Prospective, Double-Blind, Placebo-Controlled Trial of Terlipressin for Type 1 Hepatorenal Syndrome
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Supported in part by a grant from the FDA (Office of Orphan Products Grant 1R01FD003024-01) and in part by Orphan Therapeutics.
This is original work and is not under consideration for publication elsewhere. This work has been presented in part at the annual meeting of the American Association for the Study of Liver Diseases (AASLD) in Boston in November 2006. The study was registered at www.clinicaltrials.gov (ClinicalTrials.gov identifier NCT00089570).
A.J.S. and T.B. contributed equally to the writing of the manuscript.
Conflicts of interest and financial disclosures: Arun J. Sanyal, MBBS, MD: Stipends paid by Orphan Therapeutics to maintain the 24-hour study Medical Hotline (June 2004, $12,000; May 2005, $12,000). Reimbursement for travel costs and data reviews for FDA meetings (2006, $501.90; April 2007, $251.67). Thomas Boyer, MD: Reimbursement for travel costs and data reviews for FDA meetings (February 2004, $1157.90; June 2006, $377.70; October 2006, $699.20; March 2007, $389.60). Honorarium for OT-0401 Steering Committee in 2004 ($1350.00). Guadalupe Garcia-Tsao, MD: Honorarium for OT-0401 Steering Committee in 2004 ($750.00). Frederick Regenstein, MD: Honorarium for OT-0401 Steering Committee in 2004 ($750.00). Lorenzo Rossaro, MD: Honorarium for OT-0401 Steering Committee in 2004 ($750.00). Andres Blei, MD: None. Veit Gülberg, MD: None. Beate Appenrodt, MD: None. Samuel Sigal, MD: None. Peter Teuber, PhD: President and Managing Partner of Orphan Therapeutics, LLC (OT-0401 study cosponsor).
PII: S0016-5085(08)00245-X
doi:10.1053/j.gastro.2008.02.014
© 2008 AGA Institute. Published by Elsevier Inc. All rights reserved.
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- Vasoconstrictor Therapy for the Hepatorenal Syndrome

