Pioglitazone vs. Placebo in Association With Pegylated Interferon and Ribavirin in HCV Patients With Insulin Resistance

Insulin Resistance Clinical Trial

— PEGLIST C  

Official title:

ANRS HC 22, PEGLIST-C, Multicenter, Randomized Controlled Trial of Pioglitazone vs. Placebo in Association With Pegylated Interferon and Ribavirin in Patients With Chronic Hepatitis C, Non 2 or 3 Genotypes and Insulin Resistance

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00927290
• Other study ID #: 2008-006225-14
• Status: Terminated
• Phase: Phase 3
• First received: June 22, 2009
• Last updated: January 23, 2017
• Start date: December 3, 2009
• Est. completion date: July 6, 2012

Study information

• Verified date: January 2017
• Source: French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test whether the correction of insulin resistance with pioglitazone, will improve the response to antiviral treatment.

Description:

In patients infected with genotypes 1, 4, 5 and 6, the response rate to antiviral therapy remains suboptimal (less than one in two patients have a sustained virological response), which justifies the search for strategies optimizing the results of antiviral therapy. Some factors associated with non response have been identified. Among the modifiable factors, numerous series have shown that insulin resistance adversely impacts the rate of sustained virological response. The aim of this study is to determine whether the pharmacological correction of insulin resistance through therapy with glitazones restores higher rates of viral eradication and to determine the impact on the kinetics of viral response. Patients will be randomized to receive pioglitazone or placebo starting 4 months before initiating pegylated interferon and ribavirin and continued throughout the whole antiviral treatment period.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 40
• Est. completion date: July 6, 2012
• Est. primary completion date: July 6, 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years old or older

• Chronic HCV infection documented by PCR with genotype HCV-1, 4, 5 or 6

• Naive Patient(never treated with antivirals for HCV)

• HOMA score higher than 2.5

• Patient for which the investigator decided to start antiviral treatment for chronic hepatitis C

Exclusion Criteria:

• Cardiovascular disease: heart failure stage NYHA II, III or IV, unstable angina, myocardial infarction in the previous year, cardiac surgery or stroke

• Alcohol consumption exceeding 40 g / day

• Decompensated liver disease: Child-Pugh B 8 or higher, or one of the following :

bilirubin over 35 mol / L, TP below 50%, ascites, encephalopathy

• Hepatocellular carcinoma or any other neoplasm (except if in remission for > 5 years)

• Other documented chronic liver disease

• Insulin treated diabetes

• HBV or HIV co-infection infection confirmed

• Thrombocytopenia below 50 000/mm ³; neutropenia below 750/mm ³ or hemoglobin below 11 g / dL

• Drug-induced steatosis(tamoxifen, glucocorticosteroids, amiodarone, tetracyclines).

• Bone marrow or solid organ transplantation

• Pregnancy or breastfeeding, or desire for pregnancy during the study period.

• Patients under legal protection or unable to express their consent

Related Conditions & MeSH terms

• Chronic Hepatitis C
• Hepatitis
• Hepatitis A
• Hepatitis C
• Hepatitis C, Chronic
• Hepatitis, Chronic
• Insulin Resistance

Intervention

Drug:
• Pioglitazone
Pioglitazone, 45 mg QD (30 mg QD the first month)
• Placebo
Placebo 45 mg QD (30 mg QD the first month)

Locations

Country	Name	City	State
France	Hôpital Pitié Salpêtrière, Service d'hépatogastroentérologie	Paris

Sponsors (1)

Lead Sponsor	Collaborator
French National Agency for Research on AIDS and Viral Hepatitis

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Decrease in the HOMA score below 2 after 4 months of treatment with pioglitazone or placebo(at W16). The efficiency is defined as a higher proportion of subjects with HOMA <2 in the pioglitazone group than in the group treated with placebo pioglitazone.		W16
Secondary	Kinetics of decrease in viral response to pegylated interferon. Early virological response rates. Rates of sustained virological response. Effect on steatosis		EVR at W16 and W28 SVR at W88