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NCT04663737 · ClinicalTrials.gov registry record · Phase 2

Evaluating Safety, Pharmacokinetics and Clinical Benefit of Silmitasertib (CX-4945) in Subjects With Moderate COVID-19

A Phase 2 study of Covid19, sponsored by Senhwa Biosciences.

Completed
Registry status
Phase 2
Development phase
20
Enrollment target
1
Study location

NCT04663737 is a Phase 2 study of Covid19 that has completed, run by Senhwa Biosciences. The registered enrollment target is 20 participants, below the 2,702-participant average among 94 other Covid19 trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04663737, a Phase 2 study of Covid19, has completed, sponsored by Senhwa Biosciences.

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

This single-center, open-label, 2 arm parallel-group, randomized, interventional prospective exploratory study in 20 subjects aimed to evaluate safety and explore putative clinical benefits of Silmitasertib 1000 mg BID dose in patients with moderate COVID-19. Two-arm trial comparing the SOC/supportive care alone to the SOC/supportive care with addition of Silmitasertib (allocation ratio 1:1).

Conditions Studied

Interventions

  • DRUG Silmitasertib
  • DRUG SOC

Study Locations (1)

Georgia

  • Center for Advanced Research and Education - Gainesville

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2020-11-30
Est. Completion 2021-10-04
Phase Phase 2

Sponsor

Senhwa Biosciences

4 total trials

What the Registry Record Tells You About NCT04663737

The ClinicalTrials.gov registry entry for NCT04663737 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,702-participant average among 94 other Covid19 trials with a reported enrollment target (99% lower). The listed sponsor is Senhwa Biosciences, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Covid19 appearing as the primary indexed condition, and to 2 interventions - of which Silmitasertib is the first listed.

NCT04663737 reports 1 study location spanning 1 distinct geographic area - top geographies include Georgia.

Frequently Asked Questions

What is clinical trial NCT04663737 about?

NCT04663737 is a clinical study titled "Evaluating Safety, Pharmacokinetics and Clinical Benefit of Silmitasertib (CX-4945) in Subjects With Moderate COVID-19". This single-center, open-label, 2 arm parallel-group, randomized, interventional prospective exploratory study in 20 subjects aimed to evaluate safety and explore putative clinical benefits of Silmitasertib 1000 mg BID dose in patients with moderate COVID-19. Two-arm trial comparing the SOC/supporti...

What is the current status of trial NCT04663737?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2020-11-30. Estimated completion is 2021-10-04.

What conditions does trial NCT04663737 study?

This clinical trial studies the following conditions: Covid19.

What interventions are being tested in trial NCT04663737?

The interventions under investigation include: Silmitasertib (DRUG), SOC (DRUG).

Who is sponsoring clinical trial NCT04663737?

This trial is sponsored by Senhwa Biosciences, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04663737 being conducted?

This trial has 1 study location across Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.