Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04900038 · ClinicalTrials.gov registry record · Phase 2

A Clinical Trial of GSK3640254 + Dolutegravir (DTG) in Human Immunodeficiency Virus-1 Infected Treatment-naive Adults

A Phase 2 study, sponsored by ViiV Healthcare.

Terminated
Registry status
Phase 2
Development phase
85
Enrollment target

NCT04900038: Clinical Trial Phase 2 study, sponsored by ViiV Healthcare.

NCT04900038 is a Phase 2 study that was terminated before completion, run by ViiV Healthcare. The registered enrollment target is 85 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (36% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04900038, a Phase 2 study, was terminated before completion, sponsored by ViiV Healthcare.

TERMINATED
Registry status
Phase 2
Development phase
85 participants
Enrollment target

Study Summary

The purpose of this study was to evaluate the efficacy of GSK3640254 + DTG relative to lamivudine (3TC) + DTG in treatment-naïve adult participants living with human immunodeficiency virus (HIV)-1. The participants were randomized to one of the three doses of blinded GSK3640254 (100, 150, or 200 milligrams \[mgs\]) or a reference arm of blinded 3TC-each in combination with open label DTG.

Primary Outcome

Percentage of participants with plasma HIV-1 RNA \<50 c/mL at Week 24 using the Food and Drug Administration (FDA) snapshot algorithm was assessed to evaluate the antiviral activity in HIV-1 infected ART (anti-retroviral therapy)-naïve participants.

Interventions

  • DRUG Dolutegravir
  • DRUG GSK3640254
  • DRUG Lamivudine capsules
  • DRUG Lamivudine tablets

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2021-08-18
Est. Completion 2023-05-11
Phase Phase 2
ViiV Healthcare

182 total trials

Why NCT04900038 stopped before completion

NCT04900038 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 85 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (36% lower).

The record links to 0 conditions, and to 4 interventions - of which Dolutegravir is the first listed.

NCT04900038 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04900038 about?

NCT04900038 is a clinical study titled "A Clinical Trial of GSK3640254 + Dolutegravir (DTG) in Human Immunodeficiency Virus-1 Infected Treatment-naive Adults". The purpose of this study was to evaluate the efficacy of GSK3640254 + DTG relative to lamivudine (3TC) + DTG in treatment-naïve adult participants living with human immunodeficiency virus (HIV)-1. The participants were randomized to one of the three doses of blinded GSK3640254 (100, 150, or 200 mil...

What is the current status of trial NCT04900038?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 85 participants. The study started on 2021-08-18. Estimated completion is 2023-05-11.

What interventions are being tested in trial NCT04900038?

The interventions under investigation include: Dolutegravir (DRUG), GSK3640254 (DRUG), Lamivudine capsules (DRUG), Lamivudine tablets (DRUG).

Who is sponsoring clinical trial NCT04900038?

This trial is sponsored by ViiV Healthcare, which has 182 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04900038's enrollment target sits among peer trials

85 820th of 2000 higher than 1,179 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00842283 · 85 participants

    Role of Angiogenesis in Dermatologic Diseases: A Potential Therapeutic Target

  • NCT02133196 · 85 participants · Phase 2

    T Cell Receptor Immunotherapy for Patients With Metastatic Non-Small Cell Lung Cancer

  • NCT03823144 · 85 participants · NA

    Intravital Microscopy in Human Solid Tumors

  • NCT03875638 · 85 participants · Phase 2

    Treating Hyperexcitability in AD With Levetiracetam

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04900038, the US trial registry maintained by the National Library of Medicine. NCT04900038 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.