A Pivotal Clinical Study to Investigate Efimosfermin Alfa in Participants With Biopsy-confirmed F2- or F3-stage MASH

Last updated:
2026-08-01
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View trial details

Overview

Official protocol title:

A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, 3-ARM STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF EFIMOSFERMIN ALFA IN PARTICIPANTS WITH BIOPSY-CONFIRMED F2- OR F3-STAGE METABOLIC DYSFUNCTION-ASSOCIATED BOLIC DYSFUNCTION-ASSOCIATED STEATOHEPATITIS (MASH) (ZENITH-1)

Intervention/treatment:
GSK6519754 (EFIMOSFERMIN ALFA)
Medical condition:
METABOLIC DYSFUNCTION-ASSOCIATED STEATOHEPATITIS
Protocol code:
301160
Control number:
500035
Status:
Recruiting
Approved:
April 29, 2026
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT07221227
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 75 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
US GSK Clinical Trials Call Center
Role
CONTACT
Phone:
877-379-3718
Name
EU GSK Clinical Trials Call Center
Role
CONTACT
Phone:
+44 (0) 20 89904466
Sponsor
GLAXOSMITHKLINE INC

Locations

Quebec

GSK Investigational Site
Québec, Quebec, G1N 4V3
RECRUITING
Name
US GSK Clinical Trials Call Center
Role
CONTACT
Phone:
877-379-3718
Name
EU GSK Clinical Trials Call Centre
Role
CONTACT
Phone:
+44 (0) 20 8990 4466
Name
Pascale Chouinard
Role
PRINCIPAL_INVESTIGATOR
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