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Merck Receives Complete Response Letter From The U.S. FDA For Supplemental Biologics License Applications For Keytruda Six-Week Dosing Schedule
Merck's Keytruda Combination Therapy Met Main Goal In Metastatic Triple-Negative Breast Cancer Study
Merck Announces Q4 GAAP Earnings Per Share Of $0.92
Merck & Co., Inc. is a global healthcare company. The Company offers health solutions through its prescription medicines, vaccines, biologic therapies and animal health products. It operates through four segments: Pharmaceutical, Animal Health, Healthcare Services and Alliances. The Company's Pharmaceutical segment includes human health pharmaceutical and vaccine products marketed either directly by the Company or through joint ventures. Human health pharmaceutical products consist of therapeutic and preventive agents, generally sold by prescription, for the treatment of human disorders. The Company sells its human health pharmaceutical products primarily to drug wholesalers and retailers, hospitals, government agencies and managed healthcare providers, such as health maintenance organizations, pharmacy benefit managers and other institutions. Vaccine products consist of preventive pediatric, adolescent and adult vaccines, primarily administered at physician offices.
2000 Galloping Hill Rd
Kenneth C. Frazier
Chairman of the Board, President, Chief Executive Officer
Robert M. Davis
Executive Vice President, Global Services, Chief Financial Officer
Steven C. Mizell
Executive Vice President, Chief Human Resources Officer, Human Resources
Executive Vice President, Chief Information and Digital Officer
Michael T. Nally
Executive Vice President, Chief Marketing Officer
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* PRESS RELEASE - ELANCO SIGNS AGREEMENT WITH MERCK ANIMAL HEALTH TO DIVEST WORLDWIDE RIGHTS FOR VECOXAN®
* MERCK’S KEYTRUDA® (PEMBROLIZUMAB) IN COMBINATION WITH CHEMOTHERAPY MET PRIMARY ENDPOINT OF PROGRESSION-FREE SURVIVAL (PFS) AS FIRST-LINE TREATMENT FOR METASTATIC TRIPLE-NEGATIVE BREAST CANCER (MTNBC)
* ADURO BIOTECH ANNOUNCES MILESTONE ACHIEVED UNDER MERCK COLLABORATION FOR INITIATION OF PHASE 2 TRIAL OF ANTI-CD27 AGONIST MK-5890 IN NON-SMALL CELL LUNG CANCER
Merck & Co Inc <MRK.N> said on Wednesday it will spin off its women's health, biosimilar drugs and older products into a separate publicly traded company as it tightens its focus on growth drivers like cancer drug Keytruda and vaccines.
U.S. drugmaker Merck & Co Inc said on Wednesday it was planning to spin off its women's health, biosimilar drugs and legacy products into a new publicly traded company.
The U.S. Food and Drug Administration said on Wednesday it approved Merck & Co Inc's Keytruda for a hard-to-treat form of bladder cancer, making it the first new treatment for the cancer in more than two decades.
The U.S. Food and Drug Administration said on Wednesday it approved Merck & Co Inc's Keytruda for the treatment of a type of bladder cancer.
* GENOWAY ACQUIRES ADDITIONAL RIGHTS TO DEVELOP ALL ANIMAL CELL MODELS USING THE CRISPR/CAS9 SYSTEM
Merck & Co said a phase 3 trial of cancer drug Keytruda in combination with chemotherapy showed an increase in the amount of time patients lived with small cell lung cancer without it getting worse, but did not extend overall survival.
* MERCK’S KEYTRUDA® (PEMBROLIZUMAB) IN COMBINATION WITH CHEMOTHERAPY SIGNIFICANTLY IMPROVED PROGRESSION-FREE SURVIVAL COMPARED TO CHEMOTHERAPY ALONE AS FIRST-LINE TREATMENT FOR EXTENSIVE STAGE SMALL CELL LUNG CANCER
Dec 30 - AstraZeneca Plc and Merck & Co's ovarian cancer drug, Lynparza, was approved by U.S. regulators for the treatment of advanced pancreatic cancer in patients with BRCA gene mutations, the British drugmaker said on Monday.
Merck & Co <MRK.N> said on Friday it expects to make licensed doses of its recently approved Ebola vaccine available in the third quarter of 2020 and price the single-dose injection at the lowest possible access price for poor and middle-income countries.
Merck & Co said on Friday it expects to make licensed doses of its recently approved Ebola vaccine available in the third quarter of 2020 and price the single-dose injection at the lowest possible access price for poor and middle-income countries.
The U.S. Food and Drug Administration said on Thursday it approved drugmaker Merck & Co's <MRK.N> Ebola vaccine Ervebo, making it the first FDA-authorised vaccine against the deadly virus.
* Indexes down: Dow 0.3%, S&P 500 0.22%, Nasdaq 0.26% (Updates to late afternoon)
Merck & Co Inc <MRK.N> said on Monday it would buy ArQule Inc <ARQL.O> for $2.7 billion, as it looks to tap into the drug developer's experimental blood cancer therapy that targets genetic mutations.
Merck & CO said on Monday it would buy cancer drug developer ArQule Inc for $2.7 billion in cash to beef up its portfolio of blood cancer treatments.
AstraZeneca Plc <AZN.L> and Merck & Co Inc <MRK.N> said on Thursday that their drug, Lynparza, won approval in China as a first line treatment for a form of ovarian cancer.
Merck & Co Inc <MRK.N said on Monday an experimental treatment being developed with Bayer AG for patients with worsening chronic heart failure met the main goal of a late-stage study.
Merck & Co Inc <MRK.N said on Monday an experimental treatment being developed with Bayer AG for patients with worsening chronic heart failure met the main goal of a late-stage study. The drug, vericiguat, reduced the risk of heart failure and hospitalization in patients...
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