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NCT04750278 · ClinicalTrials.gov registry record · Phase 2

A Phase 2/3 Study to Evaluate FP-025 in Patients With Severe to Critical COVID 19

A Phase 2 study, sponsored by Foresee Pharmaceuticals Co..

Terminated
Registry status
Phase 2
Development phase
90
Enrollment target

NCT04750278: Clinical Trial Phase 2 study, sponsored by Foresee Pharmaceuticals Co..

NCT04750278 is a Phase 2 study that was terminated before completion, run by Foresee Pharmaceuticals Co.. The registered enrollment target is 90 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04750278, a Phase 2 study, was terminated before completion, sponsored by Foresee Pharmaceuticals Co..

TERMINATED
Registry status
Phase 2
Development phase
90 participants
Enrollment target

Study Summary

This is a Phase 2/3, randomized, double blind, placebo controlled, multicenter study to evaluate the efficacy and safety of FP-025 in adult patients with severe to critical COVID 19 with associated ARDS.

Primary Outcome

Percentage of patients alive and not requiring non-invasive or invasive ventilation at Day 28

Interventions

  • DRUG Placebo
  • DRUG FP-025 100 mg
  • DRUG FP-025 300 mg

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2021-04-06
Est. Completion 2022-04-18
Phase Phase 2
Foresee Pharmaceuticals Co.

5 total trials

Why NCT04750278 stopped before completion

NCT04750278 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower).

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

NCT04750278 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04750278 about?

NCT04750278 is a clinical study titled "A Phase 2/3 Study to Evaluate FP-025 in Patients With Severe to Critical COVID 19". This is a Phase 2/3, randomized, double blind, placebo controlled, multicenter study to evaluate the efficacy and safety of FP-025 in adult patients with severe to critical COVID 19 with associated ARDS.

What is the current status of trial NCT04750278?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 90 participants. The study started on 2021-04-06. Estimated completion is 2022-04-18.

What interventions are being tested in trial NCT04750278?

The interventions under investigation include: Placebo (DRUG), FP-025 100 mg (DRUG), FP-025 300 mg (DRUG).

Who is sponsoring clinical trial NCT04750278?

This trial is sponsored by Foresee Pharmaceuticals Co., which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04750278's enrollment target sits among peer trials

90 772nd of 2000 higher than 1,199 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 NCT04750278, the US trial registry maintained by the National Library of Medicine. NCT04750278 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.