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NCT02781584 · ClinicalTrials.gov registry record · Phase 2

Safety, Tolerability, and Efficacy of Selonsertib, Firsocostat, and Cilofexor in Adults With Nonalcoholic Steatohepatitis (NASH)

A Phase 2 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 2
Development phase
220
Enrollment target

NCT02781584: Completed Phase 2 study, sponsored by Gilead Sciences.

NCT02781584 is a Phase 2 study that has completed, run by Gilead Sciences. The registered enrollment target is 220 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02781584, a Phase 2 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 2
Development phase
220 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate the safety and tolerability of selonsertib, firsocostat, cilofexor, fenofibrate and/or Vascepa® in adults with nonalcoholic fatty liver disease (NAFLD) or nonalcoholic steatohepatitis (NASH).

Primary Outcome

Treatment-emergent AEs were defined as events that met 1 or both of the following criteria: * Any AEs with onset dates on or after the study drug start date and no later than 30 days after permanent discontinuation of study drug * Any AEs leading to premature discontinuation of study drug

Interventions

  • DRUG SEL
  • DRUG FIR
  • DRUG CILO
  • DRUG FENO
  • DRUG VAS

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2016-06-13
Est. Completion 2020-12-17
Phase Phase 2
Gilead Sciences

504 total trials

What the finished NCT02781584 record still lists

NCT02781584 is an interventional study that assigns participants to a tested intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% higher).

The record links to 0 conditions, and to 5 interventions - of which SEL is the first listed.

NCT02781584 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02781584 about?

NCT02781584 is a clinical study titled "Safety, Tolerability, and Efficacy of Selonsertib, Firsocostat, and Cilofexor in Adults With Nonalcoholic Steatohepatitis (NASH)". The primary objective of this study is to evaluate the safety and tolerability of selonsertib, firsocostat, cilofexor, fenofibrate and/or Vascepa® in adults with nonalcoholic fatty liver disease (NAFLD) or nonalcoholic steatohepatitis (NASH).

What is the current status of trial NCT02781584?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 220 participants. The study started on 2016-06-13. Estimated completion is 2020-12-17.

What interventions are being tested in trial NCT02781584?

The interventions under investigation include: SEL (DRUG), FIR (DRUG), CILO (DRUG), FENO (DRUG), VAS (DRUG).

Who is sponsoring clinical trial NCT02781584?

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 NCT02781584's enrollment target sits among peer trials

220 275th of 2000 higher than 1,718 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 NCT02781584, the US trial registry maintained by the National Library of Medicine. NCT02781584 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.