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Data updated: May 24, 2026

Gilead Sciences

GILD Biotech

Antiviral specialist with dominant HIV franchise (Biktarvy, Descovy) and hepatitis C cures. Expanding into oncology through acquisitions.

$28.4B
Revenue (2024)
$115.0B
Market Cap
-
Trials
3
New Drugs (2yr)
Modality:
20 Small Molecules 2 Biologics
Novel Drugs (2016-2024):
6 Novel Approvals 2 First-in-Class 2 Orphan Drug 4 Breakthrough

Gilead Sciences at a Glance

  • Leading 27 drug targets across portfolio
  • Fast trial execution (23 months median completion)

Upcoming FDA Decisions

Full Calendar →
Aug 27, 2026 — bictegravir and lenacapavir (BIC LEN)

Recent FDA Approvals

New drug approvals (NDA/BLA) in the last 2 years. Shows novel drugs only, excluding generics and label supplements.

Therapeutic Areas

Disease areas where this company has approved drugs and active pipeline. Weighted by commercial stage: approved drugs count most, followed by late-stage trials.

Infectious Disease 61%
16 drugs Phase 3: 102 Phase 2: 114 Phase 1: 49
Oncology 22%
1 drugs Phase 3: 30 Phase 2: 41 Phase 1: 69
Immunology 9%
2 drugs Phase 3: 16 Phase 2: 16 Phase 1: 11
Respiratory 6%
2 drugs Phase 3: 9 Phase 2: 7 Phase 1: 9
Cardiovascular 3%
1 drugs Phase 3: 3 Phase 2: 8 Phase 1: 4

Pipeline Snapshot

Active clinical trials across all therapeutic areas. Data from ClinicalTrials.gov.

160
Phase 3
186
Phase 2
142
Phase 1

Phase 3 Readout Calendar Pro

8 Phase 3 trials with confidence-graded primary completion dates.

Full calendar →
Q2 2026
Seladelpar 10 mg
Primary Biliary Cholangitis
Estimated · stale NCT06060665
Q4 2026
Sacituzumab Govitecan-hziy
Metastatic Breast Cancer
Estimated · fresh NCT04639986
Q1 2027
Sacituzumab Govitecan-hziy
Triple Negative Breast Cancer
Estimated · aging NCT05382286
Unlock 5 more readouts with confidence-graded estimates
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • BIKTARVY leads revenue
  • 5 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Infectious Disease pipeline focus
  • 8 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis
View patent timeline →

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison
Compare with competitor →

Execution Intelligence

  • Phase 3: 115/161 completed
  • Speed: 23 months avg
Unlock Full Intelligence

Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges