Safety, Tolerability, Pharmacokinetics and Activity of GS-9450 in Adults With Non-Alcoholic Steatohepatitis (NASH)

Nonalcoholic Steatohepatitis Clinical Trial

Official title:

A Phase 2, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Investigate the Safety, Tolerability, Pharmacokinetics and Activity of GS 9450 in Adults With Non-Alcoholic Steatohepatitis (NASH)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00740610
• Other study ID #: GS-US-228-0101
• Status: Completed
• Phase: Phase 2
• First received: August 21, 2008
• Last updated: January 3, 2014
• Start date: August 2008
• Est. completion date: September 2009

Study information

• Verified date: January 2014
• Source: Gilead Sciences
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationFrance: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
• Study type: Interventional

Clinical Trial Summary

The overall purpose of this study is to examine the safety, tolerability, pharmacokinetics (how the body processes a drug), and activity of GS-9450 in preventing liver damage due to scarring, or fibrosis, caused by Non-Alcoholic Steatohepatitis (also known as NASH).

Description:

This is a Phase 2, randomized, double-blind, parallel group, placebo controlled, multicenter study investigating the safety, tolerability, pharmacokinetics and activity of multiple oral doses of GS 9450 in adults with NASH. Approximately 110 subjects 18 75 years of age with elevated ALT (> 60 U/L at screening), fatty liver on screening ultrasound, and biopsy-proven NASH will be randomized (1:1:1:1:1) to one of five parallel treatment groups (22 subjects per treatment group) as follows:

GS-9450 1mg by mouth (PO) once daily, GS-9450 5 mg PO once daily, GS-9450 10 mg PO once daily, GS-9450 40 mg PO once daily, or Matching placebo PO once daily Qualifying subjects will be stratified by the presence/absence of type 2 diabetes (i.e., on/off oral diabetic medication at entry) and by geographic region (US and France). Following randomization, subjects will return within five business days later for a baseline visit, at which time they will be dispensed study medication and enter a 4-week treatment phase. Upon completion of the treatment phase, subjects will enter a 4 week off-treatment follow-up period. Each subject's participation in the study will last up to approximately 12 weeks (inclusive of screening, treatment phase, and off-treatment follow-up period).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 124
• Est. completion date: September 2009
• Est. primary completion date: August 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• 18-75 years of age

• ALT > 60 U/L

• fatty liver on screening ultrasound

• and biopsy-confirmed NASH

• platelet count >/= 75,000/mm3 and adequate hematologic function (absolute neutrophil count >/= 1,500/mm3, hemoglobin >/= 11.0 g/dL)

• calculated creatinine clearance >/= 70 mL/min

• non-insulin dependent diabetes for < 10 years is allowed if stably managed for at least 6 months prior to screening

• stable weight (no weight loss > 4%) for 8 weeks prior to screening and should maintain consistent diet, food intake, and physical exercise during the study

• must have been on stable therapy for at least 3 months prior to screening if receiving 3-hydroxy-3-methylglutaryl-coenzyme (HMG-CoA) reductase inhibitors, niacin, fibrates, vitamin E or angiotensin receptor blockers

• must have been on a stable treatment regimen for at least 3 months prior to screening if receiving other drugs possibly associated with hepatic adverse events (e.g., isoniazid, itraconazole, ketoconazole, rifabutin, rifampin, and other agents with significant hepatotoxic potential)

Exclusion Criteria:

• Insulin dependent diabetes mellitus, treatment with sulfonylureas (may be allowed pending results from a drug-drug interaction study), subjects receiving glitazones at screening or within 6 months of screening, presence of diabetic peripheral neuropathy or gastroparesis

• A > 4% decrease in weight within 8 weeks of screening

• cirrhosis or decompensated liver disease (defined as conjugated bilirubin > 1.5 x the upper limit of the normal range (ULN), prothrombin time > 1.5 x ULN, serum albumin < 3.0 g/dL, or prior history of clinical hepatic decompensation

• presence of other form of liver disease other than NASH

• history of excess alcohol ingestion, averaging > 3 drinks/day in the previous 2 years; or current alcohol intake averaging > 2 drinks/day for females and > 3 drinks per day for males; history of or current binge drinking

• serological evidence of co-infection with hepatitis B virus (HBV), hepatitis C virus (HCV), or HIV

• evidence of hepatocellular carcinoma (i.e., a-fetoprotein > 50 ng/mL)

• history of ingesting drugs possibly associated with hepatic steatosis within the past year

• history of total parenteral nutrition within the past 6 months

• prior history of gastroplasty, jejunoileal, or jejunocolonic bypass surgery

• history of ingesting drugs within the past 3 months that may improve NASH and associated fibrosis

• significant gastrointestinal disease that would interfere with absorption of oral medications; inflammatory bowel disease

• major surgery within the past year

• clinically significant abnormalities on ECG or other ECG findings that the investigator considers a safety risk

• significant systemic or major illnesses other than liver disease that, in the opinion of the investigator, would preclude treatment and adequate follow up

• prior or current malignancy involving any organ system and skin cancer (previously excised basal cell carcinoma allowed)

• acute ongoing infection, or symptoms of infection

• pregnant or breastfeeding females

• acute substance abuse within the past year.

• history of ingesting anti-TNFa drugs or immunomodulators within the past 3 months

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Fatty Liver
• Nonalcoholic Steatohepatitis

Intervention

Drug:
• GS-9450
GS-9450 capsules at a dose of 1, 5, 10, and 40 mg administered orally once daily
• GS-9450 Placebo
Placebo to match GS-9450 administered orally once daily

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Gilead Sciences

Countries where clinical trial is conducted

United States,  France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Participants Who Experienced Adverse Events (AEs) and Graded Laboratory Abnormalities		Baseline to Post-treatment Week 24	No
Secondary	Pharmacokinetics of GS-9450 and its metabolites	Pharmacokinetics (Cmax, Tmax, Cmin, ?z, t1/2, AUCtau, Vdss/F, and CL/F) measured by plasma sampling	Weeks 2 and 4	No
Secondary	Change from baseline in alanine aminotransferase (ALT)		Baseline to Week 4	No