Effects of Belapectin, an Inhibitor of Galectin-3, in Patients With Nonalcoholic Steatohepatitis With Cirrhosis and Portal Hypertension

被引:228
作者
Chalasani, Naga [1 ]
Abdelmalek, Manal F. [2 ]
Garcia-Tsao, Guadalupe [3 ]
Vuppalanchi, Raj [1 ]
Alkhouri, Naim [4 ]
Rinella, Mary [5 ]
Noureddin, Mazen [6 ]
Pyko, Maxmillan [1 ]
Shiffman, Mitchell [7 ,8 ]
Sanyal, Arun [9 ]
Allgood, Adam [10 ]
Shlevin, Harold [10 ]
Horton, Rex [10 ]
Zomer, Eliezer [10 ]
Irish, William [11 ]
Goodman, Zachary [12 ]
Harrison, Stephen A. [13 ]
Traber, Peter G. [10 ]
机构
[1] Indiana Univ Sch Med, 702 Rotary Circle,Suite 225, Indianapolis, IN 46202 USA
[2] Duke Univ, Durham, NC USA
[3] Yale Univ, New Haven, CT USA
[4] Texas Liver Inst, San Antonio, TX USA
[5] Northwestern Univ, Chicago, IL 60611 USA
[6] Cedar Sinai Med Ctr, Los Angeles, CA USA
[7] Liver Inst Virginia, Richmond, VA USA
[8] Liver Inst Virginia, Newport News, VA USA
[9] Virginia Commonwealth Univ, Richmond, VA USA
[10] Galectin Therapeut, Alpharetta, GA USA
[11] East Carolina Univ, Greenville, SC USA
[12] Inova Fairfax Hosp, Falls Church, VA USA
[13] Pinnacle Res Inst, San Antonio, TX USA
关键词
NAFLD; Carbohydrate-Binding Protein; Inflammation; Steatosis; VENOUS-PRESSURE GRADIENT; FATTY LIVER-DISEASE; AMERICAN ASSOCIATION; PRACTICE GUIDANCE; MANAGEMENT; EXPRESSION; DIAGNOSIS; PLACEBO; MODELS;
D O I
10.1053/j.gastro.2019.11.296
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Increased levels of galectin 3 have been associated with nonalcoholic steatohepatitis (NASH) and contribute to toxin-induced liver fibrosis in mice. GR-MD-02 (belapectin) is an inhibitor of galectin 3 that reduces liver fibrosis and portal hypertension in rats and was safe and well tolerated in phase 1 studies. We performed a phase 2b, randomized trial of the safety and efficacy of GR-MD-02 in patients with NASH, cirrhosis, and portal hypertension. METHODS: Patients with NASH, cirrhosis, and portal hypertension (hepatic venous pressure gradient [HVPG] >= 6 mm Hg) from 36 centers were randomly assigned, in a double-blind manner, to groups that received biweekly infusions of belapectin 2 mg/kg (n = 54), 8 mg/kg (n = 54), or placebo (n = 54) for 52 weeks. The primary endpoint was change in HVPG (Delta HVPG) at the end of the 52-week period compared with baseline. Secondary endpoints included changes in liver histology and development of liver-related outcomes. RESULTS: We found no significant difference in Delta HVPG between the 2 mg/kg belapectin group and placebo group (-0.28 mm HG vs 0.10 mm HG, P = 1.0) or between the 8 mg/kg belapectin and placebo group (-0.25 mm HG vs 0.10 mm HG, P = 1.0). Belapectin had no significant effect on fibrosis or nonalcoholic fatty liver disease activity score, and liver-related outcomes did not differ significantly among groups. In an analysis of a subgroup of patients without esophageal varices at baseline (n = 81), 2 mg/kg belapectin was associated with a reduction in HVPG at 52 weeks compared with baseline (P = .02) and reduced development of new varices (P = .03). Belapectin (2 mg/kg) was well tolerated and produced no safety signals. CONCLUSIONS: In a phase 2b study of 162 patients with NASH, cirrhosis, and portal hypertension, 1 year of biweekly infusion of belapectin was safe but not associated with significant reduction in HVPG or fibrosis compared with placebo. However, in a subgroup analysis of patients without esophageal varices, 2 mg/kg belapectin did reduce HVPG and development of varices.
引用
收藏
页码:1334 / +
页数:17
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