Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
ACTIVE NOT RECRUITING
NCT05220358
PHASE4

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

View on ClinicalTrials.gov

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

DRUG

Fostemsavir 600 MG [Rukobia]

FTR 600 mg PO BID added to daily suppressive HIV regimen

Locations (1)

Orlando Immunology Center

Orlando, Florida, United States