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NCT05894564 · ClinicalTrials.gov registry record · Phase 3

ACTIV-6: COVID-19 Study of Repurposed Medications - Arm E (Fluvoxamine 100)

A Phase 3 study of COVID-19, sponsored by Susanna Naggie, MD.

Completed
Registry status
Phase 3
Development phase
1,208
Enrollment target
20
Study locations

NCT05894564: Completed Phase 3 study of COVID-19, sponsored by Susanna Naggie, MD.

NCT05894564 is a Phase 3 study of COVID-19 that has completed, run by Susanna Naggie, MD. The registered enrollment target is 1,208 participants, below the 38,461-participant average among 298 other COVID-19 trials with a reported enrollment target (97% lower). The trial reports 20 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05894564, a Phase 3 study of COVID-19, has completed, sponsored by Susanna Naggie, MD.

COMPLETED
Registry status
Phase 3
Development phase
1,208 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study is to evaluate the effectiveness of repurposed medications (study drug(s) in reducing symptoms of non-hospitalized participants with mild to moderate COVID-19. Participants will receive either study drug or placebo. They will self-report any new or worsening symptoms or medical events they may experience while taking study drug or placebo. This study is intended to be all remote with no in person visits, unless the study team feels it is in the best interest of a participant to see them in person. Prior and current drug arms are listed on clinicaltrials.gov and will be updated with the activation of any new drug arms. Each study arm will also have its own clinicaltrials.gov entry and will include "Pro00107921" in the Unique Protocol ID.

Primary Outcome

Time to sustained recovery was the number of days between receipt of study drug and the third of 3 consecutive days without symptoms. Participants who died, by definition, did not recover regardless of reported symptom freedom. The reported summary is the median survival time.

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Fluvoxamine

Study Locations (20)

Florida

  • Arena Medical Group - Deerfield Beach
  • Lupus Foundation of Gainesville - Gainesville
  • University of Florida Health - Gainesville
  • L and A Morales Healthcare, Inc - Hialeah
  • University of Florida-JAX-ASCENT - Jacksonville
  • AMRON Vitality and Wellness Center, LLC - Jacksonville
  • Sunshine Walk In Clinic - Lake Mary
  • Lakeland Regional Medical Center - Lakeland
  • Jackson Memorial Hospital - Miami
  • University of Miami - Miami

Arizona

  • Lamb Health, LLC - Gilbert
  • First Care Medical Clinic - Mesa
  • Trident Health Center - Peoria

California

  • Hoag Memorial Hospital Presbyterian - Newport Beach
  • Assuta Family Medical Group APMC - North Hollywood
  • Stanford - Palo Alto

Colorado

  • Doctors Medical Group of Colorado Springs, P.C. - Colorado Springs
  • Pine Ridge Family Medicine Inc. - Colorado Springs

Connecticut

  • Tabitha B. Fortt, M.D., LLC - Stamford

District of Columbia

  • George Washington University Hospital - Washington D.C.

Trial Details

FieldValue
Enrollment Target 1,208 participants
Start Date 2022-08-25
Est. Completion 2023-05-30
Phase Phase 3
Susanna Naggie, MD

8 total trials

What the finished NCT05894564 record still lists

NCT05894564 is an interventional study that assigns participants to a tested intervention. Its 1,208 participants enrollment target places it among the larger protocols in the corpus, below the 38,461-participant average among 298 other COVID-19 trials with a reported enrollment target (97% lower).

The record links to 1 condition, with COVID-19 appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT05894564 names 20 study sites across 6 states, led by Florida, Arizona, California.

Frequently Asked Questions

What is clinical trial NCT05894564 about?

NCT05894564 is a clinical study titled "ACTIV-6: COVID-19 Study of Repurposed Medications - Arm E (Fluvoxamine 100)". The purpose of this study is to evaluate the effectiveness of repurposed medications (study drug(s) in reducing symptoms of non-hospitalized participants with mild to moderate COVID-19. Participants will receive either study drug or placebo. They will self-report any new or worsening symptoms or med...

What is the current status of trial NCT05894564?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,208 participants. The study started on 2022-08-25. Estimated completion is 2023-05-30.

What conditions does trial NCT05894564 study?

This clinical trial studies the following conditions: COVID-19.

What interventions are being tested in trial NCT05894564?

The interventions under investigation include: Placebo (OTHER), Fluvoxamine (DRUG).

Who is sponsoring clinical trial NCT05894564?

This trial is sponsored by Susanna Naggie, MD, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05894564 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Connecticut, District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for COVID-19

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05894564's enrollment target sits among peer trials

1,208 62nd of 298 higher than 237 of 298 other COVID-19 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other COVID-19 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 NCT05894564, the US trial registry maintained by the National Library of Medicine. NCT05894564 (large enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.