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NCT Number: NCT07719491

Study of GS-0415 and How It Works in People With HIV

The goals of this clinical study are to learn more about the study drug GS-0415, safety, tolerability, and pharmacokinetics (PK) of single ascending doses (SAD) and multiple ascending doses (MAD) of subcutaneous (SC) and intravenous (IV) GS-0415 in people with HIV-1 (PWH) on antiretroviral treatment.

The primary objectives of this study are to evaluate the safety and tolerability of escalating, single and multiple subcutaneous (SC) and intravenous (IV) doses of GS-0415, administered in PWH who are virologically suppressed on antiretroviral therapy (ART) and to evaluate the pharmacokinetics (PK) of GS-0415.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Age ≥ 18 years and age ≤ 65 years at screening
  • On stable antiretroviral (ARV) treatment for ≥ 12 consecutive months prior to screening, throughout the duration of study treatment and follow-up
  • The following ARV agents are not allowed as part of the current ART regimen: entry inhibitors (maraviroc, enfuvirtide, ibalizumab, or fostemsavir)
  • Plasma HIV-1 RNA < 50 copies/mL at screening with at least 2 documented HIV-1 RNA <50 copies/mL within the last 12 months.
  • Clusters of differentiation 4 (CD4) count ≥ 350 cells/μL
  • Weight ≥ 50 kg and ≤ 110 kg at screening and Day 1
  • Body mass index (BMI) ≥ 18.5 kg/m2 and ≤ 35 kg/m2 at screening and Day 1

Key Exclusion Criteria:

  • Documented history of pre-ART CD4 nadir < 100 cells/μL. Unknown pre-ART CD4 nadir is acceptable
  • Known to have initiated ART within 6 months of HIV infection. Unknown time between infection and ART initiation is acceptable
  • Females who are pregnant or breastfeeding or who may wish to become pregnant during the study or within 42 days after last study drug administration
  • Have chronic hepatitis B virus (HBV) as determined by either:
  • Positive HBV surface antigen, regardless of HBV core antibody status, at the Screening visit
  • Positive HBV core antibody and negative HBV surface antibody, regardless of HBV surface antigen status, at the Screening visit
  • Have active hepatitis C virus (HCV) infection:

1.) Positive anti-HCV antibody and negative HCV polymerase chain reaction (PCR) results are acceptable

  • Have a history of any of the following:

2.) Significant serious skin disease, such as but not limited to rash, food allergy, eczema, psoriasis, or urticaria

3.) Significant drug sensitivity or drug allergy ('but not limited to anaphylaxis or drug-induced liver injury)

4.) Known hypersensitivity to the study drugs, their metabolites, or to formulation excipients

5.) Previous or current history of bleeding disorder, platelet disorder including unexplained acute or chronic thrombocytopenia

6.) Autoimmune diseases including Type 1 diabetes mellitus

7.) Serious or active medical or psychiatric illness that would interfere with participant treatment, assessment, or compliance with the protocol.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Treatment and study plan

GS-0415

Drug

Administered SC or IV

GS-0415 Placebo

Drug

Administered SC or IV

Primary outcomes

  1. Percentage of Participants Experiencing Treatment-Emergent Adverse Events (AEs)

    Time frame: First dose date up to 99 days

  2. Percentage of Participants Experiencing Clinical Laboratory Abnormalities

    Time frame: First dose date up to 99 days

  3. Serum Pharmacokinetic (PK) Parameter (After Single Ascending Dose (SAD)): AUCinf of GS-0145

    Time frame: Up to 43 days

    AUCinf is defined as the area under the concentration versus time curve extrapolated to infinite time, calculated as AUClast + (Clast/λz).

  4. Serum PK Parameters (SAD): Cmax of GS-0145

    Time frame: Up to 43 days

    Cmax is defined as the maximum observed concentration of drug.

  5. Serum PK Parameters Multiple Ascending Dose (MAD): Dose 1 and Dose 5: AUCtau of GS-0145

    Time frame: Up to 99 days

    AUCtau is defined as the area under the concentration versus time curve over the dosing interval.

  6. Serum PK Parameters MAD: Dose 1 and Dose 5: Cmax of GS-0145

    Time frame: Up to 99 days

Secondary outcomes

  1. Percentages of participants With of Treatment-Emergent Anti-GS-0415 Antibodies

    Time frame: Up to 99 days

  2. Percentages of participants With Virological Rebound (Human Immunodeficiency Virus Type 1 (HIV-1) Ribonucleic Acid (RNA) ≥ 50 copies/mL)

    Time frame: Up to 99 days

Study contacts

Contact information is provided by the study sponsor or research team.

Gilead Clinical Study Information Center

CONTACT

[email protected]

1-833-445-3230 (GILEAD-0)

Sponsors and collaborators

Lead sponsor

Gilead Sciences

Industry

Registry information

Official study title

A First-in-Human Phase 1b, Single-Blind, Placebo-controlled Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate Safety and Pharmacokinetics of GS-0415 in People With HIV-1 Who Are Virologically Suppressed on Antiretroviral Treatment

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jul 22, 2026
Registry last updated
Jul 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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