CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 44 enrolled
Drug / intervention
VH4004280 +4 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06039579
NCT06039579Phase 2Completed

A Randomized, Double-Blind (Sponsor Unblinded), Placebo-Controlled, Phase 2a Trial to Investigate the Antiviral Effect, Safety, Tolerability and Pharmacokinetics of Orally Administered Investigational Capsid Inhibitor Monotherapy in HIV-1 Infected Treatment-Naïve Adults

ViiV Healthcare·interventional·Posted Sep 15, 2023·Updated Sep 30, 2025

In Brief

A Phase 2 clinical trial evaluating VH4004280, VH4011499, and 3 other interventions for HIV Infections. Completed, enrolled 44 participants across 20 sites in 9 countries.

Detailed Summary

The primary purpose of the study is to evaluate the antiviral activity of orally administered VH4004280 and VH4011499 monotherapy over 10 days in human immunodeficiency virus (HIV-1) infected Treatment-Naïve (TN) participants.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHIV Infections
CountriesArgentina, Canada, France, Germany, Italy, Mexico, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
202420252026
First PostedSep 15, 2023
Enrollment StartOct 25, 2023
Primary CompletionJun 24, 2024
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 2.8 years ago

Interventions

VH4004280drug

VH4004280 was administered as tablets orally at Day 1.

VH4011499drug

VH4011499 was administered as tablets orally at Day 1 and Day 6.

VH4004280 Matching Placebodrug

VH4004280 Matching Placebo was administered as tablets orally at Day 1.

VH4011499 Matching Placebodrug

VH4011499 Matching Placebo was administered as tablets orally at Day 1 and Day 6.

Antiretroviral therapydrug

Antiretroviral therapy was administered as available and as per investigator's recommendation.