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NCT04347239 · ClinicalTrials.gov registry record · Phase 2

Evaluate the Efficacy & Safety of Leronlimab in Patients With Severe or Critical COVID-19

A Phase 2 study, sponsored by CytoDyn.

Completed
Registry status
Phase 2
Development phase
484
Enrollment target

NCT04347239: Completed Phase 2 study, sponsored by CytoDyn.

NCT04347239 is a Phase 2 study that has completed, run by CytoDyn. The registered enrollment target is 484 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (264% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04347239, a Phase 2 study, has completed, sponsored by CytoDyn.

COMPLETED
Registry status
Phase 2
Development phase
484 participants
Enrollment target

Study Summary

The purpose of this study was assess the safety and efficacy of leronlimab (PRO 140) administered as weekly subcutaneous injection in subjects with severe or critical COVID-19 disease.

Primary Outcome

Incidence of mortality at day 28

Interventions

  • DRUG Placebo
  • DRUG Leronlimab (700mg)

Trial Details

FieldValue
Enrollment Target 484 participants
Start Date 2020-04-16
Est. Completion 2022-06-15
Phase Phase 2
CytoDyn

18 total trials

What the finished NCT04347239 record still lists

NCT04347239 is an interventional study that assigns participants to a tested intervention. The registered 484 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 (264% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04347239 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04347239 about?

NCT04347239 is a clinical study titled "Evaluate the Efficacy & Safety of Leronlimab in Patients With Severe or Critical COVID-19". The purpose of this study was assess the safety and efficacy of leronlimab (PRO 140) administered as weekly subcutaneous injection in subjects with severe or critical COVID-19 disease.

What is the current status of trial NCT04347239?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 484 participants. The study started on 2020-04-16. Estimated completion is 2022-06-15.

What interventions are being tested in trial NCT04347239?

The interventions under investigation include: Placebo (DRUG), Leronlimab (700mg) (DRUG).

Who is sponsoring clinical trial NCT04347239?

This trial is sponsored by CytoDyn, which has 18 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04347239's enrollment target sits among peer trials

484 76th of 2000 higher than 1,925 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 NCT04347239, the US trial registry maintained by the National Library of Medicine. NCT04347239 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.