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NCT04745351 · ClinicalTrials.gov registry record · Phase 3

Study to Evaluate the Efficacy and Safety of Remdesivir in Participants With Severely Reduced Kidney Function Who Are Hospitalized for Coronavirus Disease 2019 (COVID-19)

A Phase 3 study, sponsored by Gilead Sciences.

Terminated
Registry status
Phase 3
Development phase
249
Enrollment target

NCT04745351: Clinical Trial Phase 3 study, sponsored by Gilead Sciences.

NCT04745351 is a Phase 3 study that was terminated before completion, run by Gilead Sciences. The registered enrollment target is 249 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04745351, a Phase 3 study, was terminated before completion, sponsored by Gilead Sciences.

TERMINATED
Registry status
Phase 3
Development phase
249 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate whether remdesivir (RDV, GS-5734™) reduces the composite risk of death or invasive mechanical ventilation (IMV) through Day 29 in participants with severely reduced kidney function who are hospitalized for coronavirus disease 2019 (COVID-19).

Primary Outcome

This is the combined outcome measure reporting the percentage of participants with all-cause death or IMV through Day 29. The reported percentage was from the Kaplan-Meier estimate.

Interventions

  • DRUG Standard of Care
  • DRUG Remdesivir
  • DRUG RDV Placebo

Trial Details

FieldValue
Enrollment Target 249 participants
Start Date 2021-03-31
Est. Completion 2022-05-24
Phase Phase 3
Gilead Sciences

504 total trials

Why NCT04745351 stopped before completion

NCT04745351 is an interventional study that assigns participants to a tested intervention. The registered 249 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower).

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

NCT04745351 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04745351 about?

NCT04745351 is a clinical study titled "Study to Evaluate the Efficacy and Safety of Remdesivir in Participants With Severely Reduced Kidney Function Who Are Hospitalized for Coronavirus Disease 2019 (COVID-19)". The primary objective of this study is to evaluate whether remdesivir (RDV, GS-5734™) reduces the composite risk of death or invasive mechanical ventilation (IMV) through Day 29 in participants with severely reduced kidney function who are hospitalized for coronavirus disease 2019 (COVID-19).

What is the current status of trial NCT04745351?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 249 participants. The study started on 2021-03-31. Estimated completion is 2022-05-24.

What interventions are being tested in trial NCT04745351?

The interventions under investigation include: Standard of Care (DRUG), Remdesivir (DRUG), RDV Placebo (DRUG).

Who is sponsoring clinical trial NCT04745351?

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 NCT04745351's enrollment target sits among peer trials

249 1266th of 2000 higher than 735 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT04745351, the US trial registry maintained by the National Library of Medicine. NCT04745351 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.