A Phase III/IV Factorial Randomized Double-blind Trial to Compare the Addition of Dapagliflozin vs Placebo and Rosuvastatin/Ezetimibe Versus Pitavastatin in Patients With HIV on Integrase Strand Transfer Inhibitor-based Antiretrovirals With Elevated Metabolic Risk

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

People with HIV are at a higher risk of cardiovascular diseases (CVD) due to the effects of the virus and its treatment. Integrase strand transfer inhibitors (INSTIs), a common HIV treatment, are associated with increased CVD risk and metabolic issues, such as weight gain and high blood pressure. Sodium-glucose cotransporter 2 (SGLT2) inhibitors, however, have been working well in reducing CVD events and hospitalizations due to heart failure, irrespective of diabetes presence. They also help in reducing weight and blood pressure. Pitavastatin has shown to work in lowering CVD events in people with HIV, but its availability is limited. This benefit is thought to be common to all statins, but this has not yet been confirmed. This study will examine the impact of dapagliflozin vs. placebo on metabolic parameters in people with HIV with high metabolic risk who are on INSTI-based ART.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 75
Healthy Volunteers: f
View:

• Age 40-75 years and at least one of the following risk factors:

‣ BMI \> 7% increase or \> 5kg weight gain since INSTI commencement, or

⁃ BMI ≥ 30 kg/m2

• BMI ≥18 kg/m2 prior to INSTI commencement

• Currently taking INSTI-based ART

• Sustained virologic response, defined as viral load \<200 copies/mL for at least 12 months

• Current CD4 \>250 cells/mm3

• Informed consent for trial participation

Locations
Other Locations
Australia
Austin Health
RECRUITING
Melbourne
St Vincent's Hospital
RECRUITING
Sydney
India
CART-CRS
RECRUITING
Chennai
Malaysia
Universiti Malaya Medical Centre
RECRUITING
Kuala Lumpur
Nigeria
Institute of Human Virology, Nigeria
RECRUITING
Abuja
South Africa
Desmond Tutu Health Foundation
RECRUITING
Cape Town
Thailand
HIV-NAT
RECRUITING
Bangkok
Zimbabwe
University of Zimbabwe Clinical Research Centre
RECRUITING
Harare
Contact Information
Primary
Hila Haskelberg, PhD
hhaskelberg@kirby.unsw.edu.au
+61 2 9348 1607
Backup
Margaret Lowe
mlowe@kirby.unsw.edu.au
+61 2 9348 0351
Time Frame
Start Date: 2024-12-16
Estimated Completion Date: 2026-12
Participants
Target number of participants: 300
Treatments
Active_comparator: Dapagliflozin 10mg + pitavastatin 4mg
Dapagliflozin 10mg + pitavastatin 4mg given as daily tablets for 48 weeks
Active_comparator: Dapagliflozin 10mg + rosuvastatin 10mg/ezetimibe 10mg
Dapagliflozin 10mg + rosuvastatin 10mg/ezetimibe 10mg given as daily tablets for 48 weeks
Placebo_comparator: Placebo + pitavastatin 4mg
Placebo + pitavastatin 4mg given as daily tablets for 48 weeks
Placebo_comparator: Placebo + rosuvastatin 10mg/ezetimibe 10mg
Placebo + rosuvastatin 10mg/ezetimibe 10mg given as daily tablets for 48 weeks
Related Therapeutic Areas
Sponsors
Leads: Kirby Institute

This content was sourced from clinicaltrials.gov