Trials by therapeutic agent

Paxlovid (Nirmatrelvir/Ritonavir) clinical trials

9 post-viral trials on ClinicalTrials.gov · updated October 2026

Last updated 07 October 2026 from ClinicalTrials.gov. Trial statuses are refreshed automatically; check the registry record for the latest status and contact details.

9 trials3 open to enrolment1 active, not recruiting5 completed

All interventional trials in our ClinicalTrials.gov extract that list Paxlovid (Nirmatrelvir/Ritonavir) as an intervention, across Long COVID / PASC (8), Unspecified / Overlap (1). 3 are currently open to enrolment and 5 have completed. Read the OSMF evidence profile for Paxlovid (Nirmatrelvir/Ritonavir) for literature, mechanism and dosing context.

Intervention names are normalised from the registry's own arm labels, so the same compound can appear under a brand name, a generic name or a combination; check the full agent index for related entries.

⚠️
Not medical advice. This page is an automatically compiled index of entries on ClinicalTrials.gov. Listing here is not an endorsement of any trial, sponsor or treatment, and trial status can change between our refreshes. Always confirm details on ClinicalTrials.gov and discuss participation with your own clinician.

Recruiting (2)

RecruitingPhase 4 NCT06792214
Sponsor: Mount Sinai Hospital, Canada (Academic / non-profit / other)
Condition group: Unspecified / Overlap
Start: Jan 2025  |  Primary completion: Jan 2026  |  Enrollment: 118 (estimated)
Record last updated: Jan 2025

The DEFEND trial will be the world's first clinical trial to study the effectiveness of Paxlovid or Veklury in the prevention of cardiovascular post-acute sequelae of SARS-CoV-2 among hospitalized adults. Additionally, this pilot study will inform the design and conduct of a future full-scale multi-centre trial by testing the feasibility and accuracy of this study design.

View on ClinicalTrials.gov ↗
RecruitingPhase 4 NCT06441955
Sponsor: Well- Konnect Healthcare Services and Research Firm (Research network)
Intervention(s): Paxlovid (Nirmatrelvir/Ritonavir), Physiological Evaluation, Moderna Covid-19 Vaccine, Biopsychological, Behavioral, Genetic, Multidisciplinary Approach
Condition group: Long COVID / PASC
Start: Mar 2024  |  Primary completion: Sep 2030  |  Enrollment: 100 (estimated)
Record last updated: Nov 2024

Investigators are conducting a study on alternative treatments for patients who have received an current or previous positive COVID-19 diagnosis with mild-serve symptoms or undiagnosable condition after testing positive for severe acute COVID-19 infection and are experiencing long-haul symptoms.

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Not yet recruiting (1)

Not yet recruitingPhase 2 NCT07597902
Sponsor: Icahn School of Medicine at Mount Sinai (Academic / non-profit / other)
Intervention(s): Valacyclovir, Celecoxib, Paxlovid (Nirmatrelvir/Ritonavir)
Condition group: Long COVID / PASC
Start: Jun 2026  |  Primary completion: Jun 2028  |  Enrollment: 150 (estimated)
Record last updated: May 2026

The purpose of this research study is to test if the combination of three drugs, valacyclovir, celecoxib, and Paxlovid will decrease the symptoms of Long COVID in adults compared to a placebo (this does not contain the medications).

View on ClinicalTrials.gov ↗

Active, not recruiting (1)

Active, not recruitingPhase 3 NCT05852873
Sponsor: Haukeland University Hospital (Academic / non-profit / other)
Condition group: Long COVID / PASC
Start: May 2023  |  Primary completion: Sep 2025  |  Enrollment: 2000 (estimated)
Record last updated: Nov 2025

The goal of this clinical trial is to compare treatment with oral Paxlovid (nirmatrelvir/ritonavir) and placebo for acute COVID-19 as an intervention to prevent long-COVID (post-COVID-19 condition) in adults aged 18-64 years old. The main question it aims to answer is: Does treatment with Paxlovid for acute COVID-19 reduce the prevalence of long-COVID compared to placebo.

View on ClinicalTrials.gov ↗

Completed (5)

CompletedPhase 2 NCT05965726
Sponsor: Kanecia Obie Zimmerman (Academic / non-profit / other)
Condition group: Long COVID / PASC
Start: Jul 2023  |  Primary completion: Dec 2024  |  Enrollment: 964 (actual)
Record last updated: Mar 2026

This is an appendix of master protocol (NCT05595369) designed to be flexible so that it is suitable for a wide range of settings within health care systems and in community settings where it can be integrated into COVID-19 programs and subsequent treatment plans.

View on ClinicalTrials.gov ↗
CompletedPhase 2 NCT05595369
Sponsor: Kanecia Obie Zimmerman (Academic / non-profit / other)
Condition group: Long COVID / PASC
Start: Jul 2023  |  Primary completion: Aug 2024  |  Enrollment: 963 (actual)
Record last updated: Dec 2025

This study is a platform protocol designed to be flexible so that it is suitable for a wide range of settings within health care systems and in community settings where it can be integrated into COVID-19 programs and subsequent treatment plans.

View on ClinicalTrials.gov ↗
CompletedPhase 2 NCT05576662
Sponsor: Stanford University (Academic / non-profit / other)
Condition group: Long COVID / PASC
Start: Nov 2022  |  Primary completion: Aug 2023  |  Enrollment: 168 (actual)
Record last updated: Sep 2025

The purpose of this study is to compare whether being treated with nirmatrelvir plus ritonavir for 15 days works better than being treated with placebo plus ritonavir to reduce severe symptoms of Long Covid. Participants will have 5 planned visits to the study clinic over 15 weeks and will take the drug (or placebo) for the first 15 days.

View on ClinicalTrials.gov ↗
CompletedPhase 2 NCT05823896
Sponsor: Karolinska Institutet (Academic / non-profit / other)
Condition group: Long COVID / PASC
Start: May 2023  |  Primary completion: Nov 2024  |  Enrollment: 219 (actual)
Record last updated: Dec 2024

The purpose of this study is to investigate the efficacy of orally administered nirmatrelvir/ritonavir compared with placebo/ritonavir to improve quality of life in non-hospitalized adult participants suffering from post-acute COVID-19 syndrome.

View on ClinicalTrials.gov ↗
CompletedPhase 2 NCT05668091
Sponsor: Harlan M Krumholz (Academic / non-profit / other)
Condition group: Long COVID / PASC
Start: Apr 2023  |  Primary completion: Apr 2024  |  Enrollment: 100 (actual)
Record last updated: Dec 2024

This decentralized trial is a Phase 2, 1:1 randomized, double-blind, superiority, placebo-controlled study in an anticipated 100 non-hospitalized highly symptomatic adult participants with long COVID. It seeks to determine the efficacy, safety, and tolerability of 15 days of Paxlovid (nirmatrelvir/ritonavir), an anti-viral agent, compared with placebo plus ritonavir.

View on ClinicalTrials.gov ↗

Frequently asked questions

How do I join a clinical trial?

Open the trial's ClinicalTrials.gov record (the "View on ClinicalTrials.gov" button), read the Eligibility Criteria and Contacts and Locations sections, and contact the study team listed there. Trials only enrol at the sites shown in the record, so check whether a site is near you or whether the study is remote/decentralised. Your own clinician can help you judge whether a trial is a sensible option and may need to provide medical records.

What do the trial phases mean?

Early Phase 1 / Phase 1 studies test safety and dosing in a small group. Phase 2 studies look for a signal of benefit in a larger group and keep checking safety. Phase 3 studies are large confirmatory trials designed to show whether a treatment works well enough for approval. Phase 4 studies follow approved treatments after they reach the market. "Phase not applicable" is used by the registry for behavioural, device, rehabilitation and other non-drug interventions.

Does the Open Source Medicine Foundation run these trials?

No. OSMF does not sponsor, run or recruit for any trial on this page. We compile public registry entries from ClinicalTrials.gov so patients and clinicians can find them in one place. For questions about a specific study, contact the sponsor or study team listed on its ClinicalTrials.gov record.

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Cite this page
Open Source Medicine Foundation. Paxlovid (Nirmatrelvir/Ritonavir) clinical trials for Long COVID, ME/CFS and post-viral illness (9 trials, updated October 2026). Research Tracker, 07 October 2026. https://research.opensourcemed.info/trials/by-agent/paxlovid-nirmatrelvir-ritonavir.html
Underlying dataset (JSON, CC BY 4.0): https://research.opensourcemed.info/data/clinical_trials/clinical_trials_current.json. Source records: ClinicalTrials.gov.

Related: all agents · recruiting Long COVID trials · recruiting ME/CFS trials · open in trial finder.