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NCT03987074 · ClinicalTrials.gov registry record · Phase 2

Safety, Tolerability, and Efficacy of Monotherapy and Combination Regimens in Participants With Nonalcoholic Steatohepatitis (NASH)

A Phase 2 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 2
Development phase
109
Enrollment target

NCT03987074: Completed Phase 2 study, sponsored by Gilead Sciences.

NCT03987074 is a Phase 2 study that has completed, run by Gilead Sciences. The registered enrollment target is 109 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (18% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03987074, a Phase 2 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 2
Development phase
109 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate the safety and tolerability of study drug(s) in participants with nonalcoholic steatohepatitis (NASH).

Primary Outcome

Treatment-emergent adverse events (TEAEs) were defined as, any AEs with an onset date on or after the study drug start date and no later than 30 days after permanent discontinuation of study drug or any AEs leading to premature discontinuation of study drug. Participants were assessed for AEs according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

Interventions

  • DRUG Semaglutide
  • DRUG Cilofexor
  • DRUG Firsocostat

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2019-07-29
Est. Completion 2020-07-13
Phase Phase 2
Gilead Sciences

504 total trials

What the finished NCT03987074 record still lists

NCT03987074 is an interventional study that assigns participants to a tested intervention. The registered 109 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (18% lower).

The record links to 0 conditions, and to 3 interventions - of which Semaglutide is the first listed.

NCT03987074 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03987074 about?

NCT03987074 is a clinical study titled "Safety, Tolerability, and Efficacy of Monotherapy and Combination Regimens in Participants With Nonalcoholic Steatohepatitis (NASH)". The primary objective of this study is to evaluate the safety and tolerability of study drug(s) in participants with nonalcoholic steatohepatitis (NASH).

What is the current status of trial NCT03987074?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 109 participants. The study started on 2019-07-29. Estimated completion is 2020-07-13.

What interventions are being tested in trial NCT03987074?

The interventions under investigation include: Semaglutide (DRUG), Cilofexor (DRUG), Firsocostat (DRUG).

Who is sponsoring clinical trial NCT03987074?

This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03987074's enrollment target sits among peer trials

109 640th of 2000 higher than 1,361 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03987074, the US trial registry maintained by the National Library of Medicine. NCT03987074 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.