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NCT07335198

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenicity of Efimosfermin Alfa Administered as a Single Dose to Healthy Participants of Chinese, Japanese, and White/European Ancestry

Recruiting now Phase 1 Last updated 27 March 2026
What this trial tests

Phase 1 trial testing Efimosfermin alfa in Non-alcoholic Fatty Liver Disease in 30 participants. Currently enrolling.

Timeline
5 March 2026
Primary endpoint
17 August 2026
17 August 2026

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment30
Start date5 March 2026
Primary completion17 August 2026
Estimated completion17 August 2026
Sites1 location across New Zealand

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 18 to 55, any sex, with Non-alcoholic Fatty Liver Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a first time in Asia (FTIA) study designed to evaluate the safety, tolerability, pharmacokinetic (PK) and immunogenicity of efimosfermin alfa to healthy participants of Chinese, Japanese, and White/European ancestry.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Efimosfermin alfa

Trials testing the same drug.

Other recruiting trials for Non-alcoholic Fatty Liver Disease

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing