drugset / Trial / NCT06316843

Valacyclovir Plus Celecoxib for Post-Acute Sequelae of SARS-CoV-2

NCT06316843

Phase 2 Completed 59 enrolled Bateman Horne Center
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To explore the safety and efficacy of daily doses of celecoxib + valacyclovir in the treatment of patients with prolonged symptoms caused by COVID-19.

Timeline

Start
2023-10-15
Primary completion
2024-10-31
Completion
2024-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Celecoxib Other / unclassified 200 mg
Subject Valacyclovir Unknown 750 mg
Subject Valacyclovir Unknown 1500 mg

Indications