Recruiting
Phase 1

GS-0415

Sponsor:

Gilead Sciences

Code:

NCT07719491

Conditions

HIV -1 Infection

Eligibility Criteria

Sex: All

Age: 18 - 65

Healthy Volunteers: Not accepted

Interventions

GS-0415

GS-0415 Placebo

Study Details

Brief summary:

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.

Conditions

HIV -1 Infection

Study ID

NCT07719491

Start date

Jul 22, 2026

Status verified date

Sep, 2026

Completion date

Aug, 2029

Anticipated

Primary completion date

Aug, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 65

Healthy Volunteers: Not accepted

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 for ≥ 12 months before and 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:

1. Positive HBV surface antigen, regardless of HBV core antibody status, at the Screening visit
2. 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 as assessed by the investigator

3.) Significant drug sensitivity or drug allergy ('but not limited to anaphylaxis or drug-induced liver injury) as assessed by the investigator

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.

Study Design

Enrollment

112 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Group A Single Ascending Dose (SAD): GS-0415

Participants will receive single escalating doses of GS-0415 via subcutaneous (SC) or intravenously (IV) on Day 1.

experimental: Group A SAD: Placebo

Participants will receive placebo to match the single escalating doses of GS-0415 via SC or IV on Day 1.

experimental: Group B SAD: GS-0415

Participants will receive single escalating doses of GS-0415 via SC or IV on Day 1.

experimental: Group B SAD: Placebo

Participants will receive placebo to match the single escalating doses of GS-0415 via SC or IV on Day 1.

experimental: Group C Multiple Ascending Dose (MAD): GS-0415

Participants will receive escalating doses of GS-0415 via SC or IV at five different timepoints up to Date 57.

experimental: Group C MAD: Placebo

Participants will receive placebo to match escalating doses of GS-0415 via SC or IV at five different timepoints up to Day 57.

Interventions

GS-0415

Administered SC or IV

GS-0415 Placebo

Administered SC or IV

Primary outcome measure

  • Percentage of Participants Experiencing Treatment-Emergent Adverse Events (AEs) [ Time Frame: First dose date up to 99 days ]
  • Percentage of Participants Experiencing Clinical Laboratory Abnormalities [ Time Frame: First dose date up to 99 days ]
  • Serum Pharmacokinetic (PK) Parameter (After Single Ascending Dose (SAD)): AUCinf of GS-0145 [ Time Frame: Up to 43 days ]
  • Serum PK Parameters (SAD): Cmax of GS-0145 [ Time Frame: Up to 43 days ]
  • Serum PK Parameters Multiple Ascending Dose (MAD): Dose 1 and Dose 5: AUCtau of GS-0145 [ Time Frame: Up to 99 days ]
  • Serum PK Parameters MAD: Dose 1 and Dose 5: Cmax of GS-0145 [ Time Frame: Up to 99 days ]

Central Contacts and Locations

Central contacts

Gilead Clinical Study Information Center

1-833-445-3230 (GILEAD-0)GileadClinicalTrials@gilead.com

Locations

Kaiser Permanente Los Angeles Medical Center

Recruiting

Los Angeles, California, United States, 90027

Georgetown University Medical Center

Recruiting

Washington D.C., District of Columbia, United States, 20007

Floridian Clinical Research, LLC

Recruiting

Miami Lakes, Florida, United States, 33016

Triple O Research Institute, P.A.

Recruiting

West Palm Beach, Florida, United States, 33407

Emory University Hospital Midtown Infectious Disease Clinic

Recruiting

Atlanta, Georgia, United States, 30308

Centricity Research CPU - Georgia

Recruiting

Columbus, Georgia, United States, 31904

Indiana CTSI Clinical Research Center

Recruiting

Indianapolis, Indiana, United States, 46202

Brigham and Women's Hospital

Recruiting

Boston, Massachusetts, United States, 02115

Boston Medical Center

Recruiting

Boston, Massachusetts, United States, 02118

PPD Development, LP

Recruiting

Las Vegas, Nevada, United States, 89113

Jacobi Medical Center

Recruiting

The Bronx, New York, United States, 10461

Duke Early Phase Clinical Research Unit

Recruiting

Durham, North Carolina, United States, 27710

Wake Forest University Health Sciences

Recruiting

Winston-Salem, North Carolina, United States, 27157

University of Cincinnati College of Medicine

Recruiting

Cincinnati, Ohio, United States, 45267

The Ohio State University Medical Center Infectious Diseases Clinic

Recruiting

Columbus, Ohio, United States, 43210

More Information

Sponsor

Gilead Sciences

Last update posted

Sep 23, 2026

Last verified

Sep, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-19. This information was provided to ClinicalTrials.gov by Gilead Sciences on 2026-09-23. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.