GILD - Gilead Sciences, Inc.

NasdaqGS - NasdaqGS Real Time Price. Currency in USD
63.99
+0.73 (+1.15%)
At close: 4:00PM EDT

63.93 -0.06 (-0.09%)
Pre-Market: 8:15AM EDT

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Previous Close 63.26
Open 63.95
Bid 63.51 x 900
Ask 64.49 x 1800
Day's Range 63.68 - 64.49
52 Week Range 60.32 - 76.44
Volume 5,650,620
Avg. Volume 5,963,089
Market Cap 81.041B
Beta (3Y Monthly) 1.19
PE Ratio (TTM) 13.87
EPS (TTM) 4.61
Earnings Date Oct 24, 2019
Forward Dividend & Yield 2.52 (4.07%)
Ex-Dividend Date 2019-09-12
1y Target Est 80.39
Trade prices are not sourced from all markets
  • Gilead Sciences (GILD) Outpaces Stock Market Gains: What You Should Know
    Zacks

    Gilead Sciences (GILD) Outpaces Stock Market Gains: What You Should Know

    Gilead Sciences (GILD) closed the most recent trading day at $63.99, moving +1.15% from the previous trading session.

  • Startup with eye on fatty liver disease NASH lays out $70M IPO plan
    American City Business Journals

    Startup with eye on fatty liver disease NASH lays out $70M IPO plan

    A biotech company that started in Israel 21 months ago and moved to San Francisco this year wants to raise $70 million through an initial public offering to tackle one of the hottest areas of drug development. Fourteen-employee 89bio Inc. stated in a Securities and Exchange Commission filing Friday that it plans to use the cash to complete mid-stage clinical trials of its signature drug against the fatty liver disease known as nonalcoholic steatohepatitis, or NASH, and severe hypertriglyceridemia as well as for drug manufacturing. NASH has attracted deep-pocketed drug companies such as Foster City-based Gilead Sciences Inc. (NASDAQ: GILD), South San Francisco's NGM Biopharmaceuticals Inc. (NASDAQ: NGM), Pfizer Inc. (NYSE: PFE) and Intercept Pharmaceuticals Inc. (NASDAQ: ICPT) and an army of smaller companies, such as South San Francisco's Akero Therapeutics Inc. (NASDAQ: AKRO).

  • Jazz Starts CAR T-cell Linked Neurotoxicity Study Enrollment
    Zacks

    Jazz Starts CAR T-cell Linked Neurotoxicity Study Enrollment

    Jazz (JAZZ) enrolls first patient in a mid-stage study to evaluate defibrotide in prevention of neurotoxicity in relapsed/refractory DLBCL patients receiving CAR T-cell therapy.

  • Why Gilead (GILD) Could Beat Earnings Estimates Again
    Zacks

    Why Gilead (GILD) Could Beat Earnings Estimates Again

    Gilead (GILD) has an impressive earnings surprise history and currently possesses the right combination of the two key ingredients for a likely beat in its next quarterly report.

  • Gilead-Galapagos Report Efficacy & Safety Results on RA Drug
    Zacks

    Gilead-Galapagos Report Efficacy & Safety Results on RA Drug

    Gilead (GILD) announces 52-week efficacy and safety results on experimental RA drug, filgotinib, from two late-stage studies.

  • Benzinga

    The Daily Biotech Pulse: Therapix Extends Merger Deadline, Five Prime Restructures, Gilead-Galapagos Rheumatism Drug Readout

    The following is a roundup of top developments in the biotech space over the last 24 hours.  Scaling The Peaks (Biotech stocks that hit 52-week highs Oct. 10.) The Medicines Company (NASDAQ: MDCO ) Ra ...

  • Business Wire

    Gilead and Galapagos Announce Efficacy and Safety Results of Filgotinib Through 52 Weeks in FINCH 1 and FINCH 3 Studies in Rheumatoid Arthritis

    Gilead Sciences, Inc. (GILD) and Galapagos NV (Euronext & NASDAQ: GLPG) today announced that Week 52 data from the registrational Phase 3 FINCH 1 and FINCH 3 trials of filgotinib, an investigational, oral, selective JAK1 inhibitor, for the treatment of moderately-to-severely active rheumatoid arthritis (RA) are consistent with and support the efficacy, safety and tolerability profiles demonstrated in the Week 12 and 24 analyses presented earlier this year. “We are encouraged by the durability of both the efficacy and safety profiles of filgotinib seen in these studies,” said John Sundy, MD, PhD, Senior Vice President, Inflammation and Respiratory Diseases, Gilead Sciences.

  • Business Wire

    Gilead Sciences to Release Third Quarter 2019 Financial Results on Thursday, October 24, 2019

    Gilead Sciences, Inc. (GILD) announced today that its third quarter 2019 financial results will be released on Thursday, October 24, after the market closes. At 4:30 p.m. Eastern Time, Gilead’s management will host a conference call to discuss the company’s financial results for the third quarter 2019 and provide a business update. Alternatively, please call 877-359-9508 (U.S.) or 224-357-2393 (international) and dial the conference ID 6094972 to access the call.

  • Do Hedge Funds Love Gilead Sciences, Inc. (GILD)?
    Insider Monkey

    Do Hedge Funds Love Gilead Sciences, Inc. (GILD)?

    The financial regulations require hedge funds and wealthy investors that crossed the $100 million equity holdings threshold to file a report that shows their positions at the end of every quarter. Even though it isn't the intention, these filings to a certain extent level the playing field for ordinary investors. The latest round of 13F […]

  • Biotech Stock Roundup: GILD's Descovy Label Expansion Gets FDA Nod & Other Updates
    Zacks

    Biotech Stock Roundup: GILD's Descovy Label Expansion Gets FDA Nod & Other Updates

    Key highlights of the past week include label expansion of drugs, licensing deals and more.

  • Gilead (GILD) Files NDA for RA Candidate Filgotinib in Japan
    Zacks

    Gilead (GILD) Files NDA for RA Candidate Filgotinib in Japan

    Gilead's (GILD) new drug application for its JAK1 inhibitor filgotinib seeks treatment of rheumatoid arthritis in adult patients across Japan.

  • Reuters

    UPDATE 2-Humira, Rituxan top list of U.S. drugs with biggest price increases -report

    AbbVie Inc's rheumatoid arthritis drug Humira and Roche Holding AG's cancer drug Rituxan topped a list of seven treatments whose combined 2017 and 2018 price hikes accounted for a $5.1 billion increase in U.S. spending, a report released on Tuesday showed. The price hikes were more than twice the rate of medical inflation and were not supported by any new clinical evidence, the Institute for Clinical and Economic Review (ICER) said in the analysis.

  • Reuters

    REFILE-Humira, Rituxan top list of U.S. costliest drug price increases -report

    AbbVie Inc's arthritis drug Humira and Roche Holding AG's cancer drug Rituxan top the list of seven treatments whose combined 2017 and 2018 price hikes accounted for a $5.1 billion increase in U.S. spending, a report released on Tuesday showed. The price hikes were more than twice the rate of medical inflation and were unsupported by any new clinical evidence, the Institute for Clinical and Economic Review (ICER) said in the analysis.

  • Benzinga

    The Daily Biotech Pulse: D-Day For Clinuvel, Qiagen Warns Of Q3 Shortfall, Prevail Announces Gene Therapy Collaboration

    Here's a roundup of top developments in the biotech space over the last 24 hours. Scaling The Peaks (Biotech stocks hitting 52-week highs on Oct. 7) Alder Biopharmaceuticals Inc (NASDAQ: ALDR ) Celgene ...

  • Business Wire

    Gilead Sciences Submits New Drug Application for Filgotinib for the Treatment of Adults With Rheumatoid Arthritis in Japan

    Gilead Sciences, Inc. (GILD) today announced that the New Drug Application (NDA) for filgotinib, an investigational, oral, selective JAK1 inhibitor for the treatment of adults with rheumatoid arthritis (RA) has been submitted to the Japanese Ministry of Health, Labor and Welfare (MHLW). The NDA for filgotinib is supported by data from the Phase 3 FINCH clinical trial program in which once-daily treatment with filgotinib demonstrated the potential to improve clinical signs and symptoms, to achieve low disease activity and remission, and to inhibit structural damage for patients living with RA.

  • Novo Nordisk Focuses on Pipeline Development Amid Competition
    Zacks

    Novo Nordisk Focuses on Pipeline Development Amid Competition

    Novo Nordisk (NVO) has a strong presence in the Diabetes care market and focuses on the development of its pipeline amid competition.

  • MarketWatch

    Gilead Sciences names chief medical officer, from Genentech

    Gilead Sciences Inc. said Monday it named Merdad Parsey its chief medical officer, effective Nov. 1. Parsey was most recently a senior vice president of early clinical development at Roche Holding AG's Genentech Inc. Merdad will report directly to Chief Executive Daniel O'Day. The biopharmaceutical company's stock, which eased 0.3% in light premarket trading, is little changed year to date through Friday, while the iShares Nasdaq Biotechnology ETF has gained 3.2% and the S&P 500 has advanced 17.8%.

  • Business Wire

    Gilead Sciences Appoints Merdad Parsey, MD, PhD as Chief Medical Officer

    Gilead Sciences, Inc. (GILD) today announced that Merdad Parsey, MD, PhD, will join the company as Chief Medical Officer, effective November 1. Dr. Parsey will be responsible for the company’s global clinical development and medical affairs organizations. Dr. Parsey joins Gilead from Genentech, Inc., a member of the Roche Group, where he currently holds the position of Senior Vice President, Early Clinical Development in the Genentech Research and Early Development (gRED) group.

  • Gilead's Descovy HIV Regimen Gets FDA Nod for Label Expansion
    Zacks

    Gilead's Descovy HIV Regimen Gets FDA Nod for Label Expansion

    Gilead (GILD) obtains FDA approval for HIV treatment Descovy as a prevention option.

  • Gilead Stock Is Among The Biggest Biotech Stocks — But Should You Buy It?
    Investor's Business Daily

    Gilead Stock Is Among The Biggest Biotech Stocks — But Should You Buy It?

    Gilead is one of the biggest biotech companies. But recent news and earnings have been mixed. So, is Gilead stock a buy right now? Read on for a full analysis.

  • Business Wire

    Gilead Presents New Data From the Company’s HIV Clinical Development Program and Latest Findings on the Impact of HIV Pre-exposure Prophylaxis (PrEP) at IDWeek 2019

    - Results from DISCOVER Trial Provide Bone and Renal Safety Profile Data from Participants who Switched from Truvada for PrEP® to Descovy for PrEP™ -

  • Reuters

    UPDATE 1-U.S. FDA approves Gilead's Descovy for HIV prevention

    The U.S. Food and Drug Administration on Thursday approved Gilead Sciences Inc's Descovy to reduce the risk of sexually acquired HIV infection in men and transgender women who have sex with men. The approval does not include use of the drug by women to prevent HIV infection. Descovy, a combination drug, was approved in 2016 to treat people already infected with HIV.

  • Reuters

    U.S. FDA approves Gilead's HIV prevention treatment

    The U.S. Food and Drug Administration on Thursday approved Gilead Sciences Inc's drug, Descovy, to reduce the risk of sexually acquired HIV infection. The expanded label is a combination of emtricitabine and tenofovir alafenamide, and is already approved to treat chronic HIV. The drug's use excludes individuals who are at-risk of acquiring HIV from receptive vaginal sex because its effectiveness in this population has not been evaluated, the FDA said.

  • Business Wire

    U.S. Food and Drug Administration Approves Descovy® for HIV Pre-Exposure Prophylaxis (PrEP)

    Descovy for PrEP™ is indicated to reduce the risk of sexually acquired HIV-1 infection in adults and adolescents weighing at least 35 kg who are HIV-negative and at-risk for sexually acquired HIV, excluding individuals at-risk from receptive vaginal sex. “Descovy for PrEP provides a new HIV prevention option that matches Truvada’s high efficacy with statistically significant improvements in renal and bone safety, which can be an important consideration as people at risk increasingly use PrEP for longer periods of time,” said Daniel O’Day, Chairman and Chief Executive Officer, Gilead Sciences.