Phase 3 Long COVID Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are willing and able to give written consent and follow the study schedule and procedures
- People aged 18 or older at the time of screening
- People who have been diagnosed with type 2 diabetes, whether through a documented medical history, a history of taking diabetes medication, or a blood sugar result (HbA1c) of 6.5% or higher at screening
- People who are already taking a medication called dapagliflozin for their diabetes, or who are willing to take dapagliflozin 10 mg daily during the study if the lead doctor considers it appropriate
- People who developed Long COVID symptoms within 3 months of getting COVID-19, and whose symptoms have lasted for at least 2 months, from a set list of recognised Long COVID symptoms
- People whose Long COVID impact score (measured by a specific tool called the LCIT) is 30 or higher at both the screening visit and the first study day
- People who test negative for an active COVID-19 infection at both the screening visit and the first study day
- Women who could become pregnant, and men who are not sterilised and whose female partners could become pregnant, who agree to use highly effective non-hormonal contraception — or remain abstinent — throughout the study and for at least 30 days after the last dose
Who may not be able to join:
- People with advanced chronic kidney disease where the kidneys are functioning at a significantly reduced level (eGFR below 25 mL/min/1.73 m²)
- People with the most severe stage of heart failure (New York Heart Association Class IV)
- People with cirrhosis of the liver, a history of liver-related brain problems, certain enlarged veins in the food pipe or stomach, active hepatitis, a history of a specific liver bypass surgery, or certain ongoing liver diseases such as primary biliary cholangitis, untreated iron overload disorder, or primary sclerosing cholangitis
- People whose blood test results at screening show certain liver enzyme levels that are too high, abnormal bilirubin levels, signs of active hepatitis B or C infection, or a history of a positive HIV test
- People taking certain medications that strongly affect how other drugs are processed in the body, or who are taking steroid medication at a dose higher than the equivalent of 10 mg of prednisone per day
- People who have received a COVID-19 vaccine or booster within the 30 days before screening
- People who have taken part in another clinical study and received an experimental medication within the 30 days before screening
- Women who are pregnant, planning to become pregnant, or currently breastfeeding, or who have a positive pregnancy test at screening or before the first study day
- People whose safety might be at risk from taking part, or who the lead investigator does not consider able or willing to follow the study requirements
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Michael Sweeney, MD, Resverlogix Corp
Phone: (+971)429704901
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
patient acceptable symptom state (PASS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.