SARS-CoV-2 and Herpesvirus Inhibition for Ending Long COVID Dysfunction
Part of paid clinical trials in New York, New York.
- Sponsor
- Icahn School of Medicine at Mount Sinai
- Study ID
- NCT07597902
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Valacyclovir — DRUGone to two 750mg capsules taken orally in the morning and evening
- Celecoxib — DRUG200mg capsules taken orally in the morning and evening
- Paxlovid — DRUGone (100mg ritonavir tablet and two 150mg nirmatrelvir tablets) taken orally in the morning and evening
- Placebo — DRUGmatching placebo capsules and tablets taken orally in the morning and evening
Study Details
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).
Key Dates
- Start date
- Jun 1, 2026
- Status verified
- Feb 2026
- Primary completion
- Jun 30, 2028
- Completion
- Jun 30, 2028
Study Design
- Enrollment
- 150 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Combination Drug TherapyFor 14 weeks, receives valacyclovir and celecoxib initially, then addition of Paxlovid for 15 days while decreasing valacyclovir dose, and then returns to valacyclovir at the original dose later.
- Placebo Comparator: PlaceboFor 14 weeks, receives matched placebo capsules and tablets
Primary Outcome Measure
EQ-5D-5L Visual Analogue Scale (VAS) [ Time Frame: Baseline (Week 1), Week 4, Week 8, Week 12, Week 16, Week 20 ]
Central Contacts
- David Putrino, PhD212-241-7658
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Cohen Center for Recovery from Complex Chronic Illnesses (CoRE) | New York | New York | 10029 | David Putrino, PhD (PRINCIPAL_INVESTIGATOR) |
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