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Study identifier: NCT07627815 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluating the Safety and Efficacy of PNMR as Treatment for Long COVID

Condition: Long COVID  ·  Sponsor: ParagonClinicals Inc.

PhasePhase 2
Planned participants82
Who can joinAll sexes, 19 Years to no upper limit
Healthy volunteersNo

About this study

This will be a six-week, randomized, parallel, two group, open-label design. Patients will be treated with Paragon Novel Metabolic Regulator (PNMR) + standard of care (SOC) or SOC alone for 6 weeks for the treatment of Long COVID. All patients will also be provided with with Dietary \& Lifestyle recommendations specifically designed to enhance immune system function and reduce viral proliferation. Patients will be assessed in the clinic at screening/baseline, 3 and 6 weeks while on treatment, and by telephone at 4 weeks post-treatment. All patients will be asked to fill in a diary to record their daily treatment dosage when being treated with PNMR + SOC or with SOC alone. Primary objective: To evaluate the efficacy of PNMR + (SOC) vs. SOC in the treatment and management of patients with long COVID.

This description comes directly from the study's public registry record.

Talk to the study team

Samuel H. O. Bock / CSO, BA Environmental Science  ·  514 998-3935  ·  sbock@paragonsciences.com

John S Sampalis, PHD Epidemiology  ·  514 934-6116  ·  jsampalis@jssresearch.com

Always discuss trial participation with your own doctor first.

Locations (4)

Cardio HealthBrampton, Ontario, CanadaRecruiting
Cardio HealthLondon, Ontario, CanadaRecruiting
Cardio HealthMississauga, Ontario, CanadaRecruiting
Cardio HealthNorth York, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07627815