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Double-blind Study to Evaluate the Safety and Efficacy of Antroquinonol in Mild-Moderate COVID-19 Hospitalized Patients
NCT04523181 · View on ClinicalTrials.gov ↗
Study Summary
To evaluate the safety and efficacy of antroquinonol treatment of mild to moderate pneumonia due to COVID-19, as measured by the proportion of patients alive and free of respiratory failure.
Conditions Studied
Interventions
- OTHER Placebo
- DRUG Antroquinonol
Study Locations (15)
Other
- Unidad de Investigacion, Hospital Nacional IV Alberto Sabogal Sologuren-Essalud, Red Assitencial Sabogal — Callao
- Hospital de Chancay — Chancay
- Asociación Civil Selva Amazónica — Iquitos
- Hospital III Daniel Alcides Carrion - EsSalud — Tacna
Buenos Aires F.D.
- Centro Gallego — Buenos Aires
- Clinica de los Virreyes — Buenos Aires
Indiana
- Franciscan Health Michigan City — Michigan City
Kansas
- Ascension.Via Christi Research — Wichita
Maryland
- Adventist Healthcare Shady Grove Medical Center — Rockville
New Jersey
- South Jersey Infectious Disease — Somers Point
North Carolina
- Duke University Southeastern Health — Lumberton
Ciudad de Cordoba
- Sanatorio Privado Mayo SA — Córdoba
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 124 participants |
| Start Date | 2020-10-15 |
| Est. Completion | 2021-12-23 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04523181
The ClinicalTrials.gov registry entry for NCT04523181 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 124 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Golden Biotechnology Corporation, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04523181 reports 15 study locations spanning 11 distinct geographic areas — top geographies include Other, Buenos Aires F.D., Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04523181 about?
NCT04523181 is a clinical study titled "Double-blind Study to Evaluate the Safety and Efficacy of Antroquinonol in Mild-Moderate COVID-19 Hospitalized Patients". To evaluate the safety and efficacy of antroquinonol treatment of mild to moderate pneumonia due to COVID-19, as measured by the proportion of patients alive and free of respiratory failure.
What is the current status of trial NCT04523181?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 124 participants. The study started on 2020-10-15. Estimated completion is 2021-12-23.
What conditions does trial NCT04523181 study?
This clinical trial studies the following conditions: Covid-19. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04523181?
The interventions under investigation include: Placebo (OTHER), Antroquinonol (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04523181?
This trial is sponsored by Golden Biotechnology Corporation, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04523181 being conducted?
This trial has 15 study locations across Indiana, Kansas, Maryland, New Jersey, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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