Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Cost-Effectiveness of Pharmacologic Therapies for Metabolic Dysfunction-Associated Steatohepatitis With Significant Fibrosis in the United States.

Created on 25 Jun 2026

Authors

Ali A Abdeen, Turgay Ayer, Aanan Biswas, Chase J Wehrle, Sobia N Laique, Ali Aminian

Published in

Diabetes, obesity & metabolism. Jun 25, 2026. Epub Jun 25, 2026.

Abstract

The approval of new pharmacotherapies for metabolic dysfunction-associated steatohepatitis (MASH) presents a critical need for value assessment. We evaluated the cost-effectiveness of resmetirom, semaglutide and tirzepatide for U.S. adults with MASH and F2-F3 fibrosis.
We developed a Markov cohort model with a lifetime horizon from the perspective of a U.S. healthcare payer. The model simulated biopsy-confirmed patients with MASH progressing through liver-specific health states. Efficacy inputs for fibrosis regression and MASH resolution were obtained from a Bayesian network meta-analysis. Each pharmacotherapy was compared individually against standard of care; a formal sequential incremental analysis across active therapies was not performed. Cost-effectiveness was assessed against the standard of care using a $100 000/QALY willingness-to-pay threshold.
In the base-case analysis, tirzepatide had the largest QALY gain and the lowest incremental cost relative to standard of care, yielding an incremental cost-effectiveness ratio of ($42 705/QALY). Semaglutide was also cost-effective (ICER: $80 076/QALY). Resmetirom (ICER: $273 445/QALY) exceeded the WTP threshold. Drug price was the most influential parameter in sensitivity analyses; probabilistic sensitivity analysis showed a 99.5% probability of cost-effectiveness for tirzepatide and 89.8% for semaglutide at $100 000/QALY.
At current U.S. prices, tirzepatide and semaglutide are cost-effective for MASH with F2-F3 fibrosis, while resmetirom is not. The tirzepatide finding should be interpreted with caution, given that it is not yet FDA-approved for MASH and its effect estimate is based on a network meta-analysis of a phase 2 trial. Payer coverage and equitable access to MASH therapies require value-based pricing strategies.

PMID:
42348222
Bibliographic data and abstract were imported from PubMed on 25 Jun 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 7
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement