NGM282—an engineered analogue of FGF19—shows promise in patients with primary sclerosing cholangitis

The fibroblast growth factor 19 (FGF19) engineered analogue, NGM282, inhibits bile acid synthesis, decreases markers of hepatic inflammation, and significantly improves markers of fibrosis in patients with primary sclerosing cholangitis (PSC), according to the results of a Phase 2, multicentre, randomized, double-blind, placebo-controlled study reported today. The study, which involved 62 patients with PSC diagnosed according to EASL criteria,7 offers hope of a new medical treatment for a condition in which effective drug therapies are currently limited.

"Primary sclerosing cholangitis is a rare, inflammatory, cholestatic liver disease that is characterized by progressive fibrosis of the bile ducts and liver, and causes progressive liver dysfunction," explained Prof. Gideon Hirschfield from the University of Birmingham in the UK, who presented the results today at The International Liver Congress 2018 in Paris, France. "Liver transplantation is effective for advanced disease, but there are currently no medical treatments that have been shown to prolong transplant-free survival."

NGM282 is a non-tumourigenic engineered analogue of FGF19, an endocrine gastrointestinal hormone that regulates , carbohydrate and energy homeostasis. In an animal model, NGM282 was shown to suppress the classic pathway of bile acid production, and to inhibit and de novo lipogenesis. NGM282 was well tolerated in a healthy volunteer study, and the molecule has recently shown potential as a for non-alcoholic steatohepatitis (NASH).

The study presented today by Prof. Hirschfield randomized 62 patients with PSC and an elevated alkaline phosphatase (ALP) level (1.5x the upper limit of normal) to receive either a daily subcutaneous injection of NGM282 at a dose of 1 mg or 3 mg, or placebo. The primary endpoint was the change in ALP from baseline to Week 12.

Although there were no significant reductions in serum ALP levels in either active treatment group compared with placebo, at Week 12 significant reductions in serum levels of alanine aminotransferase (ALT) (-40 U/L) and aspartate aminotransferase (AST) (-23 U/L) in the NGM282 3 mg/day treatment group were observed (p<0.01 vs. placebo). Serum levels of 7α-hydroxy-4-cholesten-3-one (C4), which reflects bile acid synthesis, and total bile acid, were also significantly reduced in both NGM282 treatment groups at Week 12 compared with placebo.

"We also saw significant reductions in surrogate markers of fibrogenesis in the patients who received NGM282, with reductions especially pronounced in patients with higher-risk disease (Enhanced Liver Fibrosis Score >9.8 at baseline)", said Prof. Hirschfield. "These changes are consistent with those observed in patients with non-alcoholic steatohepatitis which were also presented at ILC this year."

NGM282 was well tolerated in this study, with no differences in PSC-related clinical events between the NGM282 treatment groups and the placebo group. No drug-induced pruritus was observed and no neutralizing anti-drug antibodies were detected during or after treatment with NGM282. The most frequently reported adverse events amongst the NGM282-treated patients were diarrhoea, frequent stools and injection site reactions, the majority of which were mild and resolved while on treatment.

"This study provides good evidence of relevant clinical activity for NGM282 in individuals with PSC and highlights the need to explore NGM282's impact on fibrosis in larger studies of a longer duration," said Prof. Hirschfield. "NGM282 seems to be a promising treatment for patients with PSC, for whom very few medical options currently exist."

"Studies like this one are key, since they investigate possible novel treatments for PSC, a disease that currently has no effective therapies," said Prof. Marco Marzioni from the University Hospital of Ancona, Italy, and EASL Governing Board Member. "Although this trial did not achieve fully positive results in terms of reduction of markers of disease progression, it certainly indicates that the manipulation of key molecules involved in the pathophysiology of PSC is the route to cure for our patients."

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Provided by European Association for the Study of the Liver
Citation: NGM282—an engineered analogue of FGF19—shows promise in patients with primary sclerosing cholangitis (2018, April 13) retrieved 8 April 2020 from
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