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

RECRUITING Phase 1

Study of GS-3242 in Participants With HIV-1; Substudy-05

NCT07001319 · View on ClinicalTrials.gov ↗

Study Summary

This study is part of a master study. The goal of master protocol (GS-US-544-5905, NCT05585307) is to learn how novel antiretrovirals (medicines that stop the virus from multiplying) affect the human immunodeficiency virus-1 (HIV-1) infection in people living with HIV (PWH). Substudy GS-US-544-5905-05 is to learn more about the study drug GS-3242 in PWH.

Conditions Studied

Interventions

  • DRUG GS-3242
  • DRUG BVY
  • DRUG Standard of Care

Study Locations (20)

Florida

  • Midland Florida Clinical Research Center, LLC — DeLand
  • AIDS Healthcare Foundation - Northpoint — Fort Lauderdale
  • Midway Immunology & Research Center, LLC — Ft. Pierce
  • BLISS Health — Orlando
  • Orlando Immunology Center, PA — Orlando
  • Triple O Research Institute, P.A. — West Palm Beach

California

  • Franco Felizarta, MD — Bakersfield
  • Ruane Clinical Research Group, Inc — Los Angeles
  • Mills Clinical Research — Los Angeles
  • Quest Clinical Research — San Francisco

Texas

  • Central Texas Clinical Research — Austin
  • Prism Health North Texas — Dallas
  • North Texas Infectious Diseases Consultant's, P.A. — Dallas
  • AXCES Research Group, LLC — El Paso

District of Columbia

  • Washington Health Institute — Washington D.C.

Georgia

  • Chatham County Health Department — Savannah

Indiana

  • Indiana University School of Medicine — Indianapolis

Michigan

  • Be Well Medical Center — Berkley

Missouri

  • KC CARE Health Center — Kansas City

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-05-29
Est. Completion 2027-02
Phase Phase 1

Sponsor

Gilead Sciences

190 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07001319

The ClinicalTrials.gov registry entry for NCT07001319 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gilead Sciences, which has 190 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with HIV-1-infection appearing as the primary indexed condition, and to 3 interventions — of which GS-3242 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07001319 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Florida, California, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07001319 about?

NCT07001319 is a clinical study titled "Study of GS-3242 in Participants With HIV-1; Substudy-05". This study is part of a master study. The goal of master protocol (GS-US-544-5905, NCT05585307) is to learn how novel antiretrovirals (medicines that stop the virus from multiplying) affect the human immunodeficiency virus-1 (HIV-1) infection in people living with HIV (PWH). Substudy GS-US-544-5905...

What is the current status of trial NCT07001319?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2025-05-29. Estimated completion is 2027-02.

What conditions does trial NCT07001319 study?

This clinical trial studies the following conditions: HIV-1-infection. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07001319?

The interventions under investigation include: GS-3242 (DRUG), BVY (DRUG), Standard of Care (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07001319?

This trial is sponsored by Gilead Sciences, which has 190 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07001319 being conducted?

This trial has 20 study locations across California, District of Columbia, Florida, Georgia, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial