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NCT07358546 · ClinicalTrials.gov registry record · Phase 1

A Study of Efimosfermin Alfa in Adults With Hepatic Impairment

A Phase 1 study, sponsored by GlaxoSmithKline.

Recruiting
Registry status
Phase 1
Development phase
32
Enrollment target

NCT07358546: Recruiting Phase 1 study, sponsored by GlaxoSmithKline.

NCT07358546 is a Phase 1 study that is actively recruiting participants, run by GlaxoSmithKline. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07358546, a Phase 1 study, is actively recruiting participants, sponsored by GlaxoSmithKline.

RECRUITING
Registry status
Phase 1
Development phase
32 participants
Enrollment target

Study Summary

This study is designed to study the pharmacokinetic (PK) and safety profiles of a single dose of efimosfermin alfa in participants with varying degrees of Hepatic Impairment (HI) (assessed by Child-Pugh score) due to steatotic liver disease, with and without significant alcohol consumption.

Interventions

  • DRUG Efimosfermin alfa

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2026-03-13
Est. Completion 2027-10-13
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What NCT07358546 shows while recruiting

NCT07358546 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 1 intervention - of which Efimosfermin alfa is the first listed.

NCT07358546 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07358546 about?

NCT07358546 is a clinical study titled "A Study of Efimosfermin Alfa in Adults With Hepatic Impairment". This study is designed to study the pharmacokinetic (PK) and safety profiles of a single dose of efimosfermin alfa in participants with varying degrees of Hepatic Impairment (HI) (assessed by Child-Pugh score) due to steatotic liver disease, with and without significant alcohol consumption.

What is the current status of trial NCT07358546?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2026-03-13. Estimated completion is 2027-10-13.

What interventions are being tested in trial NCT07358546?

The interventions under investigation include: Efimosfermin alfa (DRUG).

Who is sponsoring clinical trial NCT07358546?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07358546's enrollment target sits among peer trials

32 1296th of 2000 higher than 679 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07358546, the US trial registry maintained by the National Library of Medicine. NCT07358546 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.