Simtuzumab (SIM, GS-6624) in the Treatment of Cirrhosis Due to NASH

A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of GS-6624, a Monoclonal Antibody Against Lysyl Oxidase-Like 2 (LOXL2), in Subjects With Compensated Cirrhosis Secondary to Non-Alcoholic Steatohepatitis (NASH)

Sponsoren

Hauptsponsor: Gilead Sciences

Quelle Gilead Sciences
Kurze Zusammenfassung

The primary objective of this study is to evaluate the safety and efficacy of SIM (formerly referred to as GS-6624) in adults with compensated cirrhosis due to Non-Alcoholic Steatohepatitis (NASH). It will consist of 2 phases:

- Randomized Double-Blind Phase

- Open-Label Phase (optional)

Gesamtstatus Terminated
Anfangsdatum October 29, 2012
Fertigstellungstermin January 3, 2017
Primäres Abschlussdatum September 26, 2016
Phase Phase 2
Studientyp Interventional
Primärer Ausgang
Messen Zeitfenster
Change From Baseline in Hepatic Venous Pressure Gradient (HVPG) Baseline to Week 96
Event-Free Survival (EFS) Using Kaplan-Meier Baseline up to the time of clinical event or last dose date (maximum: 240 weeks in Blinded Phase); which ever occurred first
Einschreibung 259
Bedingung
Intervention

Interventionsart: Biological

Interventionsname: Placebo

Beschreibung: Placebo to match SIM intravenous infusion over 30 minutes every 2 weeks

Armgruppenetikett: Placebo

Interventionsart: Biological

Interventionsname: SIM

Beschreibung: Intravenous infusion over 30 minutes every 2 weeks

Anderer Name: GS-6624

Teilnahmeberechtigung

Kriterien:

Key Inclusion Criteria:

- Adults with cirrhosis of the liver defined as an Ishak fibrosis stage ≥ 5

- Liver biopsy consistent with NASH or cryptogenic cirrhosis

- Exclusion of other causes of liver disease including viral hepatitis and alcoholic liver disease

- The liver biopsy sample must be determined to be adequate for evaluation by the Central pathologist

- Must have aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 10 x the upper limit of the normal range (ULN)

- Must have serum creatinine < 2.0 mg/dL

- A negative serum pregnancy test is required for female subjects of childbearing potential

- All sexually active female subjects of childbearing potential must agree to use a protocol recommended method of contraception during heterosexual intercourse throughout the study and for 90 days following the last dose of study medication

- Lactating females must agree to discontinue nursing before starting study treatment

- Male subjects, if not vasectomized, are required to use barrier contraception (condom plus spermicide) during heterosexual intercourse from the screening through the study completion and for 90 days following the last dose of study drug

Key Exclusion Criteria:

- Pregnant or breast feeding

- Any history of hepatic decompensation including ascites, hepatic encephalopathy or variceal bleeding

- Weight reduction surgery in the past 5 year

- Child-Pugh-Turcotte (CPT) score >7; Model for End-Stage Liver Disease (MELD) score > 12 and Body Mass Index (BMI) <18kg/m2

- Positive for hepatitis C virus (HCV) RNA

- Positive for HBsAg

- Alcohol consumption greater than 21oz/week for males or 14oz/week for females

- Positive urine screen for amphetamines, cocaine or opiates (i.e. heroin, morphine) at screening. Subjects on stable methadone or buprenorphine maintenance treatment for at least 6 months prior to screening may be included in the study. Subjects with a positive urine drug screen due to prescription opioid-based medication are eligible if the prescription and diagnosis are reviewed and approved by the investigator

- Clinically significant cardiac disease

- History of malignancy, other than non-melanomatous skin cancer, within 5 years prior to screening

- Major surgical procedure within 30 days prior to screening or the presence of an open wound

- Known hypersensitivity to the investigation product or any of its formulation excipients

- History of bleeding diathesis within 6 months of screening

- Unavailable for follow-up assessment or concern for subject's compliance with the protocol procedures;

- Participation in an investigational trial of a drug or device within 30 days prior to screening

- History of solid-organ transplant; poor venous access or requirement for permanent or semi-permanent central vein catheter such as portacath

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Geschlecht: All

Mindestalter: 18 Years

Maximales Alter: 65 Years

Gesunde Freiwillige: No

Insgesamt offiziell
Nachname Rolle Zugehörigkeit
Gilead Study Director Study Director Gilead Sciences
Ort
Einrichtung:
Mayo Clinic Hospital | Phoenix, Arizona, 85054, United States
Southern California Liver Centers | Coronado, California, 92118, United States
University of California, San Diego (UCSD) | San Diego, California, 92103, United States
University of California San Francisco (UCSF) | San Francisco, California, 94143, United States
University of Colorado, Denver | Aurora, Colorado, 80045, United States
University of Miami | Miami, Florida, 33136, United States
Tampa General Hospital | Tampa, Florida, 33606, United States
Northwestern University | Chicago, Illinois, 60611, United States
Indiana University School of Medicine, Division of Gastroenterology/Hepatology | Indianapolis, Indiana, 46202, United States
Iowa Digestive Disease Center | Clive, Iowa, 50325, United States
University of Louisville | Louisville, Kentucky, 40202, United States
Tulane University | New Orleans, Louisiana, 70112, United States
Mercy Medical Center | Baltimore, Maryland, 21202, United States
Walter Reed National Military Medical Center | Bethesda, Maryland, 20889, United States
Lahey Clinic | Burlington, Massachusetts, 01805, United States
University of Mississippi Medical Center | Jackson, Michigan, 39216, United States
Minnnesota Gastroenterology, PA | Saint Paul, Minnesota, 55114, United States
Saint Louis University Hospital | Saint Louis, Missouri, 63110, United States
State University Of New York at Buffalo | Buffalo, New York, 14203, United States
North Shore University Health System | Manhasset, New York, 11030, United States
New York University | New York, New York, 10016, United States
Columbia University Medical Center | New York, New York, 10032, United States
Duke University Medical Center | Durham, North Carolina, 27710, United States
University Hospitals Case Medical Center | Cleveland, Ohio, 44106, United States
University of Pennsylvania Hospital | Philadelphia, Pennsylvania, 19104, United States
University Gastroenterology | Providence, Rhode Island, 02905, United States
Medical University of South Carolina | Charleston, South Carolina, 29425, United States
Methodist University Hospital | Memphis, Tennessee, 38104, United States
Vanderbilt University Medical Center | Nashville, Tennessee, 37212, United States
Texas Clinical Research Institute | Arlington, Texas, 76012, United States
Brooke Army Medical Center | Fort Sam Houston, Texas, 78234, United States
St. Luke Episcopal Hospital | Houston, Texas, 77030, United States
Alamo Clinical Research Associates | San Antonio, Texas, 78215, United States
Intermountain Transplant Center | Murray, Utah, 84107, United States
University of Virginia Health Center | Charlottesville, Virginia, 22908, United States
Liver Institute of Virginia | Newport News, Virginia, 23602, United States
Digestive and Liver Disease Specialists | Norfolk, Virginia, 23502, United States
Bucheon St. Marys Hospital | Richmond, Virginia, 23226, United States
Virginia Commonwealth University | Richmond, Virginia, 23298, United States
Virginia Mason Medical Center | Seattle, Washington, 98101, United States
University of Washington | Seattle, Washington, 98104, United States
University of Manitoba | Winnipeg, Manitoba, R3E 3P4, Canada
Dalhousie University | Halifax, Nova Scotia, B3H 2Y9, Canada
Toronto Liver Centre | Toronto, Ontario, M6H 3M1, Canada
Hôpital de la Croix Rousse | Lyon, 69317, France
Hospital Saint-Antoine | Paris, 75012, France
CHU Pitié-Salpêtrière | Paris, 75013, France
Fonds de Recherche Honoraires | Strasbourg, 67091, France
Gastroenterologisch-Hepatologisches Zentrum Kiel | Kiel, 24146, Germany
Eugastro Gmbh | Leipzig, 4129, Germany
Istituto Clinico Humanitas | Rozzano, Milano, 20089, Italy
Azienda Ospedaliero-Universitaria Policlinico di Modena | Modena, 41100, Italy
Azienda Ospedaliera Città della Salute e della Scienza di Torino | Torino, 10126, Italy
Fundacion De Investigacion | San Juan, 00927, Puerto Rico
Hospital Vall D´Hebron | Barcelona, Cataluna, 08035, Spain
Hospital Universitario Puerta de Hierro | Majadahonda, Madrid, 28222, Spain
Royal Free Hospital, Pond Street | London, NW3 2QG, United Kingdom
King's College Hospital NHS Trust | London, SE5 9RS, United Kingdom
Nottingham University Hospitals Queen's Medical Centre | Nottingham, NG7 2UH, United Kingdom
Standort Länder

Canada

France

Germany

Italy

Puerto Rico

Spain

United Kingdom

United States

Überprüfungsdatum

March 2019

Verantwortliche Partei

Art: Sponsor

Schlüsselwörter
Hat den Zugriff erweitert No
Bedingung Durchsuchen
Anzahl der Waffen 3
Armgruppe

Etikette: SIM 200 mg

Art: Experimental

Beschreibung: During the Randomized Double-Blind Phase, participants will receive SIM 200 mg via intravenous infusion every 2 weeks for up to 240 weeks. During the optional Open-Label Phase, participants will receive SIM 700 mg via intravenous infusion every 2 weeks for up to an additional 240 weeks.

Etikette: SIM 700 mg

Art: Experimental

Beschreibung: During the Randomized Double-Blind Phase, participants will receive SIM 700 mg via intravenous infusion every 2 weeks for up to 240 weeks. During the optional Open-Label Phase, participants will receive SIM 700 mg via intravenous infusion every 2 weeks for up to an additional 240 weeks.

Etikette: Placebo

Art: Placebo Comparator

Beschreibung: During the Randomized Double-Blind Phase, participants will receive placebo to match SIM administered via intravenous infusion every 2 weeks for up to 240 weeks. During the optional Open-Label Phase, participants will receive SIM 700 mg administered via intravenous infusion every 2 weeks for up to an additional 240 weeks.

Akronym NASH
Studiendesign Info

Zuweisung: Randomized

Interventionsmodell: Parallel Assignment

Hauptzweck: Treatment

Maskierung: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Quelle: ClinicalTrials.gov