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. 2022 Mar 2;55(9):1099–1115. doi: 10.1111/apt.16831

TABLE 1.

Selected studies of drugs for NASH cirrhosis in Phase II/III development

Agent Mechanism Phase ClinicalTrials.gov number Progress/results Date of completion or expected completion
Simtuzumab 42 Monoclonal antibody against lysyl oxidase‐like 2 IIb NCT01672879 Ineffective in decreasing hepatic venous pressure gradient Jan 2017
Selonsertib 41 Selective inhibitor of ASK1 III NCT03053063 Ineffective in improving fibrosis without worsening NASH May 2019
Emricasan 44 Pan‐caspase inhibitor II NCT03205345 No reduction in composite outcome of mortality, decompensation or rise in MELD‐NA score ≥4 points Aug 2019
Pegbelfermin 45 PEGylated fibroblast growth factor 21 (FGF21) analogue IIa NCT03486912 Ineffective in improving fibrosis without worsening NASH Oct 2021
Aldafermin Fibroblast growth factor 19 analogue II NCT04210245 Ongoing; primary outcome: ≥ 1‐stage improvement in fibrosis without worsening NASH Sep 2022
Belapectin Inhibitor of galectin 3 IIb/3 NCT04365868 Ongoing; primary outcome: proportion of patients who develop new oesophageal varices Dec 2023
Semaglutide ± Cilofexor/Firsocostat Glucagon‐like peptide‐1 receptor agonist (semaglutide) II NCT04971785 Ongoing; primary outcome: ≥1‐stage improvement in fibrosis without worsening NASH Mar 2024
Efruxifermin Fc‐ fibroblast growth factor 21 fusion protein IIb NCT05039450 Ongoing; primary outcome: change from baseline in fibrosis regression with no worsening steatohepatitis Apr 2024
BMS‐986263 siRNA designed to degrade HSP47 mRNA II NCT04267393 Ongoing; primary outcome: ≥ 1‐stage improvement in fibrosis without worsening NASH Jul 2024

Abbreviations: MELD, model for end‐stage liver disease; NASH, non‐alcoholic steatohepatitis.