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NCT07703748
Long-Term Real-World Evidence Study to Evaluate Effectiveness, Persistence, Adherence, Safety and Tolerability of Long-acting Cabotegravir Plus Rilpivirine.
Conditions: Human Immunodeficiency Virus Infection (HIV), HIV-1 Infection in Adults
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 3346
Sponsor: FUNDACIÓN HOSPITAL UNIVERSITARIO INFANTA LEONOR Y DEL HOSPITAL UNIVERSITARIO DEL SURESTE
Location: Hospital Universitario de Burgos Burgos
Summary
The RELATIVITY study is a nationwide, multicenter, ambispective observational cohort evaluating the long-term effectiveness, safety, persistence, and tolerability of long-acting injectable cabotegravir plus rilpivirine (CAB+RPV LA) in people living with HIV in Spain.
The study includes adults with HIV-1 infection who achieved virological suppression on oral antiretroviral therapy and switched to long-acting CAB+RPV as part of routine clinical care. No study-specific treatment or interventions are performed. Clinical information is collected retrospectively from treatment initiation and prospectively during routine follow-up.
The primary objectives are to evaluate long-term virological effectiveness, treatment persistence, and confirmed virological failure over five years. Secondary objectives include assessment of safety, treatment discontinuation, adherence to injection schedules, immunological outcomes, metabolic changes, patient-reported outcomes, and factors associated with treatment success or failure. The study also evaluates outcomes in clinically relevant subgroups, including older adults, women, migrants, people with obesity, individuals with multimorbidity, and those infected through vertical transmission.
Eligibility Criteria
Inclusion Criteria:
* Adults aged ≥18 years.
* Documented HIV-1 infection.
* Receiving oral antiretroviral therapy with plasma HIV-1 RNA \
Source: ClinicalTrials.gov (NCT07703748). StuddyBuddy aggregates publicly available trial information.