Contract Research & Services
Clinical Trials

Madrigal’s liver drug succeeds in phase 2 clinical trial

PBR Staff Writer Published 01 June 2018

Madrigal Pharmaceuticals has said that its MGL-3196 thyroid hormone receptor (THR) β-selective agonist achieved liver biopsy endpoints in patients with non-alcoholic steatohepatitis (NASH) at 36 weeks in phase 2 clinical trial.

The double-blind, placebo-controlled phase 2 study included 125 patients over the age of 18 and was undertaken across nearly 25 clinical sites in the US.

Patients were randomized to receive either MGL-3196 or placebo in a 2:1 ratio.

The study met the primary endpoint at week 12 and demonstrated a sustained treatment benefit at week 36.

In the study, more patients treated with MGL-3196 compared with placebo achieved a two point reduction in NAS (NAFLD activity score) on biopsy.

The company said a ≥30% fat reduction in MGL-3196 treated patients, at week 12 predicted an enhanced NASH histologic response at week 36, including 39% NASH resolution, which was statistically significant relative to placebo.

MGL-3196 was well-tolerated with mostly mild and lesser moderate adverse events.

Madrigal CEO Paul Friedman said: “The degree of NASH resolution, an approvable FDA endpoint, in patients who received MGL-3196 for 9 months we believe suggests a high likelihood of success in a larger trial with a somewhat longer treatment period in a Phase 3 study designed similarly to this Phase 2 study, pending regulatory agreement with such a design.

“Further, considering what we have learned regarding drug exposure and dosing, we believe there is potential to resolve NASH in as little as 9 months in 30-40% of patients receiving only MGL-3196, a well-tolerated once a day oral therapy.”

Madrigal said it looks forward to advance MGL-3196 in a phase 3 clinical trial in NASH patients.

The company noted that MGL- 3196 demonstrated the potential for a range of of therapeutically beneficial effects, enhancing components of both metabolic syndrome, like insulin resistance and dyslipidemia, and fatty liver disease, including lipotoxicity and inflammation.


Image: Madrigal’s MGL-3196 achieved liver biopsy endpoints in patients with NASH. Photo: courtesy of jk1991 / FreeDigitalPhotos.net.