Gilead Sciences, Inc. (VIE:GILD)

Austria flag Austria · Delayed Price · Currency is EUR
111.64
+1.60 (1.45%)
At close: Jun 26, 2026
Market Cap139.21B +16.1%
Revenue (ttm)25.79B +3.5%
Net Income7.99B +54.5%
EPS6.38 +55.4%
Shares Out n/a
PE Ratio17.42
Forward PE69.82
Dividend2.77 (2.48%)
Ex-Dividend DateJun 15, 2026
Volume217
Open109.30
Previous Close110.04
Day's Range108.94 - 111.98
52-Week Range90.30 - 131.64
Betan/a
Analystsn/a
Price Targetn/a
Earnings DateAug 7, 2026

About Gilead Sciences

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 inj... [Read more]

Industry Biological Products, Except Diagnostic Substances
Founded 1987
Employees 17,000
Stock Exchange Vienna Stock Exchange
Ticker Symbol GILD

Financial Performance

In 2025, Gilead Sciences's revenue was $29.44 billion, an increase of 2.40% compared to the previous year's $28.75 billion. Earnings were $8.51 billion, an increase of 1672.92%.

Financial numbers in USD Financial Statements

News

Merck says FDA approves Keytruda and Keytruda Qlex in combo with Trodelvy

Merck (MRK) announced the U.S. FDA approved Keytruda and Keytruda Qlex, each in combination with Trodelvy, Gilead’s (GILD) Trop-2-directed antibody-drug conjugate, for the first-line treatment of adul...

1 day ago - TheFly

U.S. FDA Approves Trodelvy® for First-Line Treatment of Metastatic Triple-Negative Breast Cancer

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the U.S. Food and Drug Administration (FDA) has approved Trodelvy® (sacituzumab govitecan-hziy), a first...

2 days ago - Business Wire

For decades, the only first treatment for one of the deadliest breast cancers was standard chemotherapy. Now there are two newly approved drugs.

AstraZeneca and Gilead have won approval for treatments of an advanced form of the disease.

2 days ago - WSJ

FDA approves Gilead’s Trodelvy for two indications

The Food and Drug Administration approved sacituzumab govitecan-hziy, or Trodelvy from Gilead Sciences (GILD), for two indications in adults with triple-negative breast cancer, the regulator announced...

2 days ago - TheFly

Gilead announces EC grants marketing authorization for Trodelvy

Gilead (GILD) Sciences announced that the European Commission has granted marketing authorization for Trodelvy as monotherapy for the treatment of adult patients with unresectable or metastatic triple...

3 days ago - TheFly

European Commission Approves Trodelvy® as a First-Line Treatment for Metastatic Triple-Negative Breast Cancer Patients Not Candidates for PD-(l)1 Inhibitors

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the European Commission (EC) has granted marketing authorization for Trodelvy® (sacituzumab govitecan-hz...

3 days ago - Business Wire

The Healthcare M&A Wave

In this week's edition of InnovationRx, we look at biotech M&A, the rise of India's Anthem Biosciences, and more. To get it in your inbox, subscribe here.

9 days ago - Forbes

Gilead announces FDA approval of sNDA for Yeztugo

Gilead (GILD) Sciences announced the U.S. FDA accepted its supplemental New Drug Application for Yeztugo 300-mg tablet as a potential once-weekly oral formulation for the prevention of HIV as pre-expo...

11 days ago - TheFly

U.S. FDA Accepts Gilead's Application for Investigational Once-Weekly Oral Yeztugo, Potentially the First Long-Acting Pill for HIV Prevention

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced the U.S. Food and Drug Administration (FDA) accepted its supplemental New Drug Application (sNDA) for Yeztugo...

11 days ago - Business Wire

Gilead announces donation of over 2,000 vials of remdesivir to Uganda

Gilead (GILD) Sciences announced a donation of more than 2,000 vials of its intravenous antiviral therapy, remdesivir, to the Republic of Uganda to support response efforts to the current outbreak…

14 days ago - TheFly

Gilead Mobilizes Rapid Donation of Remdesivir to Support Ebola Response, Building on Decade-Long Commitment to Outbreak Relief

FOSTER CITY, Calif.--(BUSINESS WIRE)-- #Ebola--Gilead Sciences today announced a donation of more than 2,000 vials of its intravenous antiviral therapy, remdesivir, to the Republic of Uganda to suppor...

14 days ago - Business Wire

National AIDS Memorial and the Gilead Foundation Launch Major Investment to Expand HIV/AIDS Education and Community Leadership

SAN FRANCISCO & FOSTER CITY, Calif.--(BUSINESS WIRE)--The National AIDS Memorial together with the Gilead Foundation today announced a transformative three-year, ~$3 million commitment to help preserv...

15 days ago - Business Wire

Healthcare ETFs: From Broad Exposure to Big Breakthroughs

With AI and space dominating many of the market's most popular investment themes, it can be difficult to find differentiated opportunities. Healthcare is often viewed as one of the more defensive sect...

15 days ago - ETF Trends

Gilead Sciences Transcript: Goldman Sachs 47th Annual Global Healthcare Conference 2026

Management highlighted a robust pipeline in virology, oncology, and inflammation, with strong HIV franchise growth and new long-acting therapies. Recent acquisitions and disciplined financial management support long-term growth, with no major patent expiries until 2036.

17 days ago - Transcripts

Merck, Gilead announce discontinuation of Phase 3 KEYNOTE-D46/EVOKE-03 study

Merck (MRK) and Gilead Sciences (GILD) announced the discontinuation of the Phase 3 KEYNOTE-D46/EVOKE-03 study investigating Gilead’s Trodelvy in combination with KEYTRUDA, Merck’s anti-PD-1 therapy, ...

18 days ago - TheFly

Gilead and Merck Announce Positive Topline Results From Two Phase 3 Studies Evaluating Islatravir/Lenacapavir, an Oral Once-Weekly HIV Treatment

FOSTER CITY, Calif., & RAHWAY, N.J.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) and Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that the primary...

18 days ago - Business Wire

Merck and Gilead Provide Update on Phase 3 KEYNOTE-D46/EVOKE-03 Study

RAHWAY, N.J. & FOSTER CITY, Calif.--(BUSINESS WIRE)---- $MRK #MRK--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Gilead Sciences, Inc. (Nasdaq: GILD) today announced the...

18 days ago - Business Wire

Gilead announces launch of lenacapavir in South Africa

Gilead (GILD) applauds the leadership of the Government of South Africa and the Global Fund for accelerating access to lenacapavir, a long-acting HIV prevention medication. This marks an important ste...

21 days ago - TheFly

Gilead Applauds Collaborative Efforts to Launch Lenacapavir for HIV Prevention in South Africa

FOSTER CITY, Calif.--(BUSINESS WIRE)-- #Access--Gilead applauds the leadership of the Government of South Africa and the Global Fund for accelerating access to lenacapavir, a long-acting HIV preventio...

21 days ago - Business Wire

Gilead Sciences and Lakefront Complete Acquisition of Ouro Medicines to Further Expand Inflammation Pipeline

FOSTER CITY, Calif. & MECHELEN, Belgium--(BUSINESS WIRE)-- #GILD--Gilead Sciences, Inc. (Nasdaq: GILD) and Lakefront Biotherapeutics NV (Euronext & Nasdaq: LKFT) today announced the successful complet...

22 days ago - Business Wire

GILEAD SCIENCES AND LAKEFRONT COMPLETE ACQUISITION OF OURO MEDICINES TO FURTHER EXPAND INFLAMMATION PIPELINE

Companies will collaborate on the development of gamgertamig, a potential first-in-class and best-in-class T cell engager in autoimmune diseases

22 days ago - GlobeNewsWire

Gilead announces results from Phase 3 study of Livdelzi

Gilead (GILD) Sciences announced results from a Phase 3 study in people with primary biliary cholangitis, showing that treatment with Livdelzi led to significantly more patients achieving normalizatio...

24 days ago - TheFly

Gilead's Livdelzi® (Seladelpar) Delivers Statistically Significant Composite ALP Normalization in Phase 3 IDEAL Trial in Primary Biliary Cholangitis (PBC)

FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced positive results from a Phase 3 study in people with primary biliary cholangitis (PBC), showing that treatmen...

24 days ago - Business Wire

Gilead Sciences Transcript: Bernstein 42nd Annual Strategic Decisions Conference

Poised for robust growth, the company expects up to 10 launches by 2027 and is expanding in HIV, oncology, and inflammation. Recent acquisitions strengthen the pipeline, while disciplined R&D and AI integration support top-tier margins and global health impact.

4 weeks ago - Transcripts

Gilead presents new Livdelzi data at EASL congress

Gilead (GILD) shared new results from a post hoc analysis showing that Livdelzi was associated with high and sustained rates of normalization of a key liver marker in people living…

4 weeks ago - TheFly