At a glance
ClinicalIndex Comparison Record- ✓Completion of 48-week pioglitazone course in protocol 01-DK-0130 with demonstrated improvements in liver histology and/or serum ALT levels
- ✓At least 48 weeks of follow-up with no thiazolidinedione therapy after protocol 01-DK-0130
- ✓Liver biopsy showing NASH with total NASH activity score of at least 4 (including score of at least 1 each for parenchymal inflammation, cellular injury, and steatosis) taken 48 weeks after stopping pioglitazone
- ✓Elevations in serum ALT levels
- ✕Hepatitis B (HBsAg positive)
- ✕Hepatitis C (HCV RNA detectable in serum)
- ✕Autoimmune hepatitis (ANA ≥1:160 with consistent histology or prior response to immunosuppressive therapy)
- ✕History of excess alcohol ingestion (>30 g/day in previous 10 years or >10 g/day in previous year)
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Long-Term Treatment of Nonalcoholic Steatohepatitis With Pioglitazone
In Brief
A Phase 2 clinical trial evaluating Actos (Pioglitazone) for Hepatitis. Completed, enrolled 18 participants across 1 site.
Detailed Summary
Nonalcoholic steatohepatitis (NASH) is a common liver disease that resembles alcoholic hepatitis but occurs in persons who drink little or no alcohol. The etiology of NASH is unclear, but it is commonly associated with diabetes, obesity, and insulin resistance. Several pilot studies, including a study of pioglitazone at the NIH Clinical Center (01-DK-0130), have shown that the insulin-sensitizing thiazolidinediones lead to decreases in serum alanine aminotransferase (ALT) levels and improved liver histology. Once therapy is stopped, however, ALT levels rapidly return to pre-treatment values. Inaddition we are currently enrolling patients with NASH in a pilot study of metformin therapy for 48-weeks, however our results in 3 patients thus far have not been very encouraging. In the current study, patients who have completed the pilot study of pioglitazone and have been off therapy for 48 weeks will be offered re-treatment for 3 years. We also propose to treat patients who have not had a satisfactory response to metformin with pioglitazone for the same duration. After a repeat medical and metabolic evaluation and liver biopsy, patients with moderate-to-severe NASH (activity score greater than or equal to 4) will restart pioglitazone at a dose of 15 mg daily. If after 48 weeks, ALT levels are not normal or improved to the degree identified during the pilot study, the dose will be increased to 30 mg daily at the end of 3 years, all patients will undergo repeat medical and metabolic evaluation and liver biopsy. The primary end point will be improvement in liver histology. Secondary end points will be improvements in insulin sensitivity, reduction in visceral fat, liver volume, and liver biochemistry. The aim of this study is to evaluate whether long-term pioglitazone therapy can safely achieve and maintain biochemical and histological improvements in NASH. ...
Study Details
Timeline
Interventions
Pts receive drug in a dose of 15 mg daily for at least 1 year; the dose is escalated to 30 mg daily if serum ALT levels do not fall to normal by the 1 year pt; if pts have a biochemical response, drug is continued for 3 years,