GSK PLC Sponsored ADR (GSK)
(Delayed Data from NYSE)
$43.55 USD
+0.54 (1.26%)
Updated Sep 16, 2024 04:00 PM ET
After-Market: $43.55 0.00 (0.00%) 6:34 PM ET
3-Hold of 5 3
A Value C Growth A Momentum A VGM
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$43.55 USD
+0.54 (1.26%)
Updated Sep 16, 2024 04:00 PM ET
After-Market: $43.55 0.00 (0.00%) 6:34 PM ET
3-Hold of 5 3
A Value C Growth A Momentum A VGM
Zacks News
Pharma Stock Roundup: AZN's Leukemia Drug Wins FDA Nod, MRK's Keytruda in Focus
by Zacks Equity Research
Label expansion of Merck's (MRK) Keytruda and FDA approval of AstraZeneca's (AZN) leukemia drug grab headlines this week
Merck Gets Priority Review for Yet Another Keytruda sBLA
by Zacks Equity Research
Merck's (MRK) sBLA to include overall survival data from a key lung cancer study on Keytruda's label gets FDA's priority review. If approved, it will expand the eligible patient population.
Gilead's Rheumatoid Arthritis Drug Successful in Phase III
by Zacks Equity Research
Gilead (GILD) and partner Galapagos' rheumatoid arthritis candidate meets all primary and key secondary endpoints in first phase III study.
Glaxo's Nucala Suffers Regulatory Setback, Gets CRL for COPD
by Zacks Equity Research
FDA issues a complete response letter to Glaxo's (GSK) application for label expansion of its asthma drug, Nucala for COPD.
Gilead, Galapagos Spondylitis Drug Meets Primary Endpoint
by Zacks Equity Research
Gilead's (GILD) ankylosing spondylitis candidate, filgotinib meets primary endpoint in phase II study.
Novartis to Sell Sandoz's Dermatology Business to Aurobindo
by Zacks Equity Research
Novartis (NVS) looks to sell Sandoz's dermatology business in the United States and generic U.S. oral solids portfolio, to Aurobindo Pharma USA Inc., for $0.9 billion.
Merck's Keytruda Gets Priority Review for Rare Skin Cancer
by Zacks Equity Research
Merck's (MRK) sBLA for Keytruda to expand its label for a rare form of skin cancer gets priority review from FDA.
Mylan Suffers Several Setbacks: What's in Store in 2H18?
by Zacks Equity Research
Mounting competition and recent setbacks cast a pall over Mylan's (MYL) near-term performance.
AstraZeneca's Lupus Drug Misses Primary Endpoint in Study
by Zacks Equity Research
AstraZeneca's (AZN) phase III study, evaluating anifrolumab in adult patients with moderate-to-severe systemic lupus erythematosus, does not meet primary endpoint.
Merck (MRK) Receives FDA Approval for Two HIV Medicines
by Zacks Equity Research
Merck's (MRK) two new HIV-1 medicines, Delstrigo and Pifeltro, get approval in the United States.
Glaxo's Asthma Drug Gets EU Nod for Pediatric Population
by Zacks Equity Research
Glaxo (GSK) gains EU approval for asthma drug Nucala as an add-on treatment for severe refractory eosinophilic asthma in children.
Pharma Stock Roundup: Approval of NVS & ABBV Cancer Drugs, MRK's HIV Drug in Focus
by Zacks Equity Research
Novartis (NVS) & AbbVie (ABBV) get cancer approvals. Merck (MRK) gets FDA nod for two new HIV medicines.
Emergent (EBS) to Buy Narcan Maker Adapt Pharma for $735M
by Zacks Equity Research
Emergent (EBS) inks a deal to buy Adapt Pharma. This move will add the latter's popular Narcan nasal spray to its portfolio.
Novartis' Tafinlar/Mekinist Combo Gets EU Nod for 3rd Disease
by Zacks Equity Research
Novartis' (NVS) BRAF/MEK inhibitor combination, Tafinlar plus Mekinist, gets approval in the EU for adjuvant treatment of BRAF V600 mutation-positive melanoma.
Gilead's CAR-T Therapy Yescarta Gets Approval in Europe
by Zacks Equity Research
Gilead's (GILD) CAR-T therapy, Yescarta gets approval in Europe for adult patients suffering from relapsed or refractory DLBCL and PMBCL, after two or more lines of systemic therapy.
Zai Lab Stock Down, Atopic Dermatitis Candidate Trial Fails
by Zacks Equity Research
Shares of Zai Lab (ZLAB) decline following the failure of a phase IIA study on its pipeline candidate, ZL-3101, for the treatment of atopic dermatitis.
Novartis' CAR-T Therapy Kymriah Gets Approval in Europe
by Zacks Equity Research
Novartis (NVS) gets EC approval for CAR-T therapy, Kymriah, for the treatment of pediatric and young adult patients up to 25 years of age with B-cell acute lymphoblastic leukemia.
AstraZeneca's Bevespi Unimpressive in Phase III COPD Study
by Zacks Equity Research
AstraZeneca's (AZN) inhaler, Bevespi Aerosphere, fails to demonstrate superiority over Glaxo's Arono in a phase III COPD study.
Novartis Breast Cancer Drug Meets Primary Goal in Phase III
by Zacks Equity Research
Novartis' (NVS) late-stage candidate, BYL719, meets primary endpoint in SOLAR trial on advanced breast cancer patients.
J&J to Appeal as Judge Confirms Jury Order in Talc Case
by Zacks Equity Research
Johnson & Johnson's (JNJ) suffers setback as Missouri judge confirms talc lawsuit jury verdict. The company intends to appeal against the decision.
Glaxo Stock Up This Year So Far: Will the Rally Continue?
by Zacks Equity Research
After a relatively strong performance so far this year, let's see how things are shaping up for Glaxo (GSK) for the rest of the year.
The Zacks Analyst Blog Highlights: IBM, Texas Instruments, Glaxo, Simon Property Group and State Street
by Zacks Equity Research
The Zacks Analyst Blog Highlights: IBM, Texas Instruments, Glaxo, Simon Property Group and State Street
Top Stock Reports for IBM, Texas Instruments & Glaxo
by Mark Vickery
Today's Research Daily features new research reports on 16 major stocks, including IBM (IBM), Texas Instruments (TXN) and Glaxo (GSK).
Mylan Suffers a Blow as Teva Gets FDA Nod for EpiPen Generic
by Zacks Equity Research
Mylan (MYL) suffers another setback as Teva wins the FDA approval of first generic version of EpiPen and EpiPen Jr (epinephrine) auto-injector for the emergency treatment of allergic reactions.
Pharma Stock Roundup: Blow for Bayer, FDA Nod for MRK Cancer Drug in New Indication
by Zacks Equity Research
Bayer's (BAYRY) Monsanto subsidiary faces $289 million fine in Roundup lawsuit. Merck/Eisai's drug Lenvima gets FDA approval to treat the most common form of liver cancer.