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

← catalyst calendar

NCT07719491 · readout ≤ 1,108 d

Sponsored by Gilead Sciences (industry) · GILD — their whole pipeline →.

Phase
Phase 1
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
112estimated

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartJul 2026estimatedWhen the study began enrolling
Primary completionAug 2029estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2029estimatedThe whole study's end, after follow-up
First posted2026-07-22actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • HIV -1 Infection

Interventions

  • Drug: GS-0415
  • Drug: GS-0415 Placebo

Primary outcomes

what the primary-completion date above is the date OF
Percentage of Participants Experiencing Treatment-Emergent Adverse Events (AEs)
measured First dose date up to 99 days
Percentage of Participants Experiencing Clinical Laboratory Abnormalities
measured First dose date up to 99 days
Serum Pharmacokinetic (PK) Parameter (After Single Ascending Dose (SAD)): AUCinf of GS-0145
measured Up to 43 days
Serum PK Parameters (SAD): Cmax of GS-0145
measured Up to 43 days
Serum PK Parameters Multiple Ascending Dose (MAD): Dose 1 and Dose 5: AUCtau of GS-0145
measured Up to 99 days
Serum PK Parameters MAD: Dose 1 and Dose 5: Cmax of GS-0145
measured Up to 99 days

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