COVID drug showdown: 3,800 patients test which pill kills virus fastest
NCT ID NCT05041907
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This phase 2 trial is testing several antiviral drugs—including Paxlovid, molnupiravir, and older drugs like hydroxychloroquine—in 3,800 adults with mild COVID-19. Participants are randomly assigned to receive one of the treatments or no antiviral drug, and researchers measure how quickly the virus clears from their throat and nose over five days. The goal is to identify which drugs speed recovery and reduce viral load, helping guide future treatment choices.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Various antiviral drugs (nirmatrelvir/ritonavir, molnupiravir, nitazoxanide, hydroxychloroquine, fluoxetine, monoclonal antibodies)
- What this could lead to
- If successful, this trial could identify which existing drugs work best to clear the virus faster in early COVID-19, helping doctors choose the most effective treatment.
- What could go wrong
- This is a mid-stage trial testing many drugs at once, so results may not confirm which is truly best. Some drugs (like hydroxychloroquine) have already shown mixed results in other studies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 3,800 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2021
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient understands the procedures and requirements and is willing and able to give informed consent for full participation in the study. * Previously healthy adults, male or female, aged 18 to 60 years at time of consent with early symptomatic COVID-19 * SARS-CoV-2 positive by lateral flow antigen test OR a positive PCR test for SARS-CoV-2 within the last 24hrs with a Ct value of less than 25 (all viral targets) * Symptoms of COVID-19 (including fever, or history of fever) for less than 4 days (96 hours). * Oxygen saturation ≥96% measured by pulse-oximetry at time of screening. * Able to walk unaided and unimpeded in ADLs * Agrees and is able to adhere to all study procedures, including availability and contact information for follow-up visits Exclusion Criteria: The patient may not enter the study if ANY of the following apply: * Taking any concomitant medications or drugs (see appendix 4)† * Presence of any chronic illness/ condition requiring long term treatment, or other significant comorbidity (e.g. diabetes, obesity but see appendix 4 for the full list) * Laboratory abnormalities discovered at screening (see appendix 4) * For females: pregnancy, actively trying to become pregnant, or lactation * Contraindication to taking, or known hypersensitivity reaction to any of the proposed therapeutics (see appendix 4) * Currently participating in another COVID-19 therapeutic or vaccine trial * Evidence of pneumonia (although imaging is NOT required) * healthy women on the oral contraceptive pill are eligible to join the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites in 4 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Bangplee Hospital
TERMINATEDMueang Samut Prakan, 10540, Thailand
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Faculty of Tropical Medicine, Mahidol University
RECRUITINGBangkok, 10400, Thailand
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Laos-Oxford-Mahosot Wellcome Trust Research Unit
RECRUITINGVientiane, 01000, Laos
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Sukraraj Tropical & Infectious Disease Hospital
RECRUITINGKathmandu, Nepal
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The Aga Khan University Hospital
TERMINATEDKarachi, Pakistan
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Universidade Federal de Minas Gerais
RECRUITINGMinas Gerais, Brazil
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Vajira hospital
TERMINATEDBangkok, 10300, Thailand
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Blood samples and health records could reveal why some COVID-19 cases turn severe
- Home antibody tests put to the test: can you read your own COVID-19 result?
- Can lung ultrasound reveal COVID-19's signature in the lungs?
- When the immune system Can't fight back: tracking three respiratory viruses
- The household maze: how does COVID-19 move between family members?