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Study identifier: NCT06724640 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of VH4011499 Compared to Placebo in Adults Without HIV

Condition: HIV Infections  ·  Sponsor: ViiV Healthcare

PhasePhase 1
Planned participants168
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

The purpose of this study is to investigate safety, pharmacokinetics and tolerability following single ascending dose (SAD) and multiple ascending doses (MAD) of VH4011499 administered subcutaneously (SC) and intramuscularly (IM) in participants without HIV.

This description comes directly from the study's public registry record.

Talk to the study team

US GSK Clinical Trials Call Center  ·  877-379-3718  ·  GSKClinicalSupportHD@gsk.com

EU GSK Clinical Trials Call Center  ·  +44 (0) 20 89904466  ·  GSKClinicalSupportHD@gsk.com

Always discuss trial participation with your own doctor first.

Locations (2)

GSK Investigational SiteLas Vegas, Nevada, United StatesRecruiting
GSK Investigational SiteAustin, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06724640