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GILD

SP100NasdaqGS

Gilead Sciences, Inc.

Healthcare · Drug Manufacturers - General · United States

$131.27
+4.21% today
Mkt Cap
$162.98B
P/E
17.86×
Fwd P/E
13.59×
Div Yield
2.50%
Beta
0.343×
52W Range
47.5%
Company profileSource: provider

Gilead Sciences, Inc., a biopharmaceutical company, discovers, develops, and commercializes medicines in the areas of unmet medical need in the United States, Europe, and internationally. The company provides Biktarvy, Descovy, Genvoya, Odefsey, Sunlenca, Symtuza, and YeztugoFor the treatment of HIV-1 infection in patients. It also provides Epclusa, Livdelzi, and Vemlidy to treat chronic hepatitis C virus, primary biliary cholangitis, and chronic hepatitis B virus; Tecartus, a T-cell therapy for the treatment of adult patients; Trodelvy, an injection for intravenous use; and Yescarta, a suspension for intravenous infusion, is a CAR T-cell therapy for the treatment of adult patients. Further, it provides AmBisome, for the treatment of serious invasive fungal infections; and Veklury for the treatment of COVID-19. Additionally, the company engages in the development of various immunotherapies for patients with cancer and other incurable diseases. The company has collaboration agreements with Shenzhen Pregene Biopharma Co., Ltd.; Abingworth; Arcus Biosciences, Inc.; Merck Sharp & Dohme Corp.; Janssen Sciences Ireland Unlimited Company; Japan Tobacco, Inc.; Everest Medicines; Merck & Co, Inc.; Tentarix Biotherapeutics Inc.; and Assembly Biosciences, Inc. It also has research collaboration, option, and license agreement with Merus N.V. for the discovery of novel dual tumor-associated antigens (TAA) targeting trispecific antibodies. The company has a collaboration with Terray Therapeutics, Inc. to discover and develop small molecule therapies; and LEO Pharma to develop, manufacture, and commercialize the small molecule oral STAT6 program. The company was incorporated in 1987 and is headquartered in Foster City, California.

www.gilead.com
By the numbersComputed from live metrics

Shares trade at a moderate 17.9× trailing earnings, easing to 13.6× on forward estimates. Profitability shows a net margin of 31.0% and return on equity of 43.4%. Leverage is modest at 0.8× net debt/EBITDA. Revenue grew 4.4% year-on-year. It yields 2.5% in dividends. The mean analyst target of USD157.67 sits 20.1% above the current price (Buy, 27 analysts).

AI analysisAI-generated · 04 Jul 2026 · claude-opus (research)

business model

Gilead Sciences is a biopharmaceutical company focused on developing and commercializing therapies, with historic leadership in antiviral treatments for HIV and viral hepatitis, plus a growing oncology franchise. Revenue is concentrated in patented, high-value drugs sold globally. Growth depends on its HIV portfolio, pipeline advancement, and oncology diversification.

revenue segments

Gilead reports primarily as a single pharmaceutical business, with product revenue concentrated in HIV therapies (led by Biktarvy and the Descovy franchise, plus long-acting agents such as lenacapavir), liver disease (hepatitis B and C), and oncology (including cell therapy via Kite's Yescarta and Tecartus, and Trodelvy). HIV generates the majority of product sales.

key dependencies

The business depends on continued HIV market leadership and Biktarvy sales, successful launch and uptake of long-acting HIV prevention (lenacapavir), pipeline and oncology execution, patent protection and exclusivity timelines, regulatory approvals, and pricing and reimbursement dynamics.

competitors

Competitors include ViiV Healthcare (GSK-led) in HIV, AbbVie and others in hepatitis, and a broad set of oncology and cell-therapy players such as Bristol Myers Squibb, Novartis, Merck, and AstraZeneca. It also faces generic competition as patents expire.

moat

Gilead's moat rests on its dominant HIV franchise, patent-protected best-in-class therapies, deep antiviral R&D expertise, established prescriber and payer relationships, and long-acting product innovation that can extend franchise durability.

risks

Risks include HIV revenue concentration and eventual patent cliffs (Biktarvy loss of exclusivity), clinical and regulatory setbacks, uncertain returns on oncology and cell-therapy investments, drug-pricing reform and reimbursement pressure, and competition including from long-acting rivals.

01

Financials & metrics

as of 04 Jul 2026
52-week rangeMid-range · 47%
Low $107.75Now $131.27High $157.29

Price is around the middle of its range. Green = nearer the yearly low, red = nearer the high — a position indicator, not a buy/sell signal.

Valuation
Profitability
Growth
Financial Health
Efficiency
Cash Flow
Per Share
Dividend
Market

Tap any metric for an explanation. provider computedN/A not available from source

Income-statement history isn't available for this security.

02

Dividends

This company does not currently pay a dividend.

03

Analyst assessment

as of 04 Jul 2026
Buy27 analysts
Implied to mean target
+20.1%
Low $122.00High $180.00
Now
$131.27
Low
$122.00
Mean
$157.67
High
$180.00
Rating distribution
Strong Buy 6
Buy 16
Hold 7
Sell 0
Strong Sell 0

Aggregate consensus only. Named per-analyst targets require a premium source and are not shown; the data model is ready to hold them if one is added.

04

Technicals

as of 02 Jul 2026
CloseSMA 50SMA 200Death cross
SMA 50
$129.60
SMA 200
$129.92
RSI (14)
62.3
MACD
-0.80
RSI (14) · overbought > 70 · oversold < 30
05

News

The FDA Just Approved a KEYTRUDA Combination That Could Become the Standard First-Line Treatment for Aggressive Breast Cancer
Merck & Co., Inc. (NYSE:MRK) is one of billionaire Cliff Asness’ top 10 healthcare stock picks. On June 25, Merck & Co., Inc. (NYSE:MRK) announced that the FDA approved both KEYTRUDA and KEYTRUDA QLEX each in combination with Gilead’s Trodelvy as a first-line treatment for adult patients with unresectable locally advanced or metastatic triple-negative breast […]
Insider Monkey · 3d ago
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KYMR Stock Soars 51% YTD on Progress of Atopic Dermatitis Drug
KYMR surges 51% year to date as KT-621 advances in atopic dermatitis and asthma, with pivotal data timelines accelerating and pipeline momentum building.
Zacks · 3d ago
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Imviva Biotech Granted FDA IDE Authorization for Cancer Treatment Trial
By Karen Roman Imviva Biotech said it has FDA authorization for its Investigational Device Exemption application to use Adaptive Biotechnologies’ clonoSEQ assay in the TENACITY-01 trial to treat leukemia/lymphoma and minimal residual disease. This authorization enables the company to use test results for patient management, identify eligible patients for enrollment, and evaluate treatment response, it […] The post Imviva Biotech Granted FDA IDE Authorization for Cancer Treatment Trial appeared f
Exec Edge · 4d ago
Read ↗
Gilead (GILD) Moves 3.3% Higher: Will This Strength Last?
Gilead (GILD) was a big mover last session on higher-than-average trading volume. The latest trend in earnings estimate revisions might not help the stock continue moving higher in the near term.
Zacks · 5d ago
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Gilead (GILD) Wins FDA Approval for Trodelvy in TNBC
Gilead Sciences, Inc. (NASDAQ:GILD) is one of the 12 Most Profitable S&P 500 Stocks to Invest In. On June 25, 2026, the Food and Drug Administration approved Trodelvy from Gilead Sciences, Inc. (NASDAQ:GILD) for two indications in adults with triple-negative breast cancer. The first approval covers sacituzumab govitecan-hziy as a single agent for the first-line […]
Insider Monkey · 6d ago
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Will Trodelvy’s First-Line TNBC Approval Redefine Gilead Sciences’ (GILD) Oncology-Led Investment Narrative?
Earlier this week, Gilead Sciences received FDA approval for an expanded use of Trodelvy, authorizing it as a first-line treatment for adults with unresectable locally advanced or metastatic triple-negative breast cancer, either alone in PD-(L)1–ineligible patients or in combination with Keytruda for PD-L1–positive tumors. This decision, underpinned by robust Phase 3 ASCENT-03 and ASCENT-04 data and reinforced by top-tier NCCN guideline endorsements, elevates Trodelvy’s role in breast cancer...
Simply Wall St. · 7d ago
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Gilead Sciences (GILD) Wins First Line Trodelvy Approval In The US And Europe
FDA approved Gilead Sciences' (NasdaqGS:GILD) Trodelvy for first line treatment of metastatic triple negative breast cancer in the US. Regulators in Europe granted a similar first line approval, creating aligned indications across key markets. Decisions follow clinical data showing survival benefits for patients treated with the Trop 2 directed antibody drug conjugate. Gilead Sciences has been known largely for its antiviral portfolio, and Trodelvy adds further weight to its growing...
Simply Wall St. · 7d ago
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Ascendis Pharma (ASND) Moves 9.9% Higher: Will This Strength Last?
Ascendis Pharma (ASND) witnessed a jump in share price last session on above-average trading volume. The latest trend in earnings estimate revisions for the stock doesn't suggest further strength down the road.
Zacks · 8d ago
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Cantor Fitzgerald Reiterates Overweight Rating on Gilead Sciences (GILD) Following Positive HIV Trial Results
Gilead Sciences Inc. (NASDAQ:GILD) ranks among the best set-it-and-forget-it stocks to buy right now. Cantor Fitzgerald restated an Overweight rating and a $155 price target for Gilead Sciences Inc. (NASDAQ:GILD) on June 9, following the company’s clinical research findings. Gilead Sciences Inc. (NASDAQ:GILD), in collaboration with Merck, revealed solid top-line results from the phase 3 […]
Insider Monkey · 8d ago
Read ↗
Gilead Sciences (GILD) Dips More Than Broader Market: What You Should Know
In the closing of the recent trading day, Gilead Sciences (GILD) stood at $123.84, denoting a -1.05% move from the preceding trading day.
Zacks · 9d ago
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