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Study details
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Study of GS-0151 in Participants With Rheumatoid Arthritis

Gilead Sciences
NCT IDNCT06902519ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

75

Study length

about 1.9 years

Ages

18–75

Locations

15 sites in AL, CA, FL +6

About this study

Researchers are testing a treatment called GS-0151 to see if it's safe and how well the body absorbs, changes, distributes, and eliminates it. The trial will last for 686 days and involve approximately 75 participants with rheumatoid arthritis.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take GS-0151
  • 2.Take Placebo
PhasePhase 1
Primary goalCohort 1, 2 and 3: Percentage of Participants Experiencing Treatment-Emergent Adverse Events (TEAEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low12%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Cohort 1, 2 and 3: Percentage of Participants Experiencing Treatment-Emergent Adverse Events (TEAEs), Cohorts 1, 2 and 3: Percentage of Participants Experiencing Serous Adverse Events (SAEs) and Adverse Events (AEs) Leading to Study Discontinuation, Cohorts 1, 2 and 3: Serum Cmax, Following the Last Dose of GS-0151, Cohorts 1, 2 and 3: Serum Tmax Following the Last Dose of GS-0151

Secondary: Cohort 3: Change From Baseline in Disease Activity Score for 28 Joint Count Using C-Reactive Protein (DAS28-CRP) at Week 12 in Participants With Moderately to Severely Active RA

Body systems

Immune