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Changes in Immunologic Parameters Following the Addition of Fostemsavir in Virologically Suppressed Immunologic Non-responders Living With HIV-the RECOVER Study
Sponsor: Orlando Immunology Center
Summary
The RECOVER study is a self-controlled case series to evaluate whether the addition of Fostemsavir (Rukobia) to a stable HIV regimen in virologically suppressed patients living with HIV who never experience optimal CD4 T-cell count recovery can result in meaningful increases in different immunologic parameters such as CD4 T-cell count, CD4 T-cell percentage and CD4/CD8 ratio
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
25
Start Date
2022-06-15
Completion Date
2026-02-13
Last Updated
2025-08-03
Healthy Volunteers
No
Conditions
Interventions
Fostemsavir 600 MG [Rukobia]
FTR 600 mg PO BID added to daily suppressive HIV regimen
Locations (1)
Orlando Immunology Center
Orlando, Florida, United States