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NCT07525544RecruitingPhase 1

A Study to Investigate the Safety and PK of VH4770359 in Healthy Participants

A Multi-part, Phase 1, First-Time-in-Human Study to Investigate Safety, Tolerability, and PK of VH4770359 in Healthy Participants

Source: ClinicalTrials.gov · Last updated 13 Jul 2026

Brief summary (registry, in English)

VH4770359 (also known as GSK4770359) is an antiretroviral compound. This first-in-human study aims to evaluate the safety, tolerability, and pharmacokinetics (PK) of orally administered VH4770359 in healthy participants. The findings from this study will support the design of future clinical studies of VH4770359 in people living with HIV.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
214 (estimated)
First submitted
6 Apr 2026
Start date
14 May 2026
Primary completion date
5 May 2027
Lead sponsor
ViiV Healthcare
Diseases
HIV
NCT number
NCT07525544

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 214
  • From 14 May 2026 to the primary completion date, 5 May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants with significant medical history that could alter drug pharmacokinetics, pose a risk, or interfere with conduct.
  • Use of prohibited medications.
  • Regular use of alcohol, drugs of abuse, tobacco, or nicotine products.
  • Exclusionary prior or concurrent clinical study participation.

Other illness

  • Has exclusionary psychiatric, hepatic, cardiovascular, gastrointestinal, respiratory, endocrine, neurological, hematological, or renal condition, or exclusionary malignancy.
  • A positive test(s) for Hepatitis B surface antigen (HBsAg) and/or anti-HBc, hepatitis C antibodies, or human immunodeficiency virus (HIV).
  • A history of or ongoing high-risk behaviors for HIV acquisition.
  • Exclusionary allergies or sensitivities.

Who the study is looking for

  • 18 to 55 years old
  • BMI 18.5-37.0 kg/m2
  • Male participants must adhere to contraception requirements or abstinence, and female participants must not be pregnant/breastfeeding and be of non-childbearing potential.

Age in the registry: 18 years to 55 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
GSK Investigational Site
Coordinator of this site? Confirm its status
BaltimoreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.