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Merck

142.38

-0.4100-0.29%

Post-market: 142.37-0.0081-0.01%19:59 EDT

Volume:8.41M

Turnover:1.19B

Market Cap:351.28B

PE:111.86

High:142.77

Open:141.90

Low:138.89

Close:142.79

52wk High:156.92

52wk Low:82.01

Shares:2.47B

Float Shares:2.47B

Volume Ratio:1.02

T/O Rate:0.34%

Dividend:3.32

Dividend Rate:2.33%

EPS(TTM):1.27

EPS(LYR):7.28

ROE:6.96%

ROA:11.87%

PB:8.38

PE(LYR):19.56

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Overview Company News Filings

FDA approves Welireg and Lenvima combo for ccRCC

Merck Shares Flat in Volume Spike After FDA Approves Kidney Drug, Last up 0.50% at $148.81

THOMSON REUTERS

FDA Approves Belzutifan in Combination with Lenvatinib for Advanced Renal Cell Carcinoma with a Clear Cell Component

THOMSON REUTERS

Merck Has Two Overlooked Pipeline Catalysts Coming Before Year-End, UBS Says

MT Newswires Live

Pharmaceutical Stocks Jump. Moderna, Eli Lilly up over 3%; Novavax, Pfizer up Around 2%; Merck, Novo Nordisk up over 1%

Tiger Newspress

Merck's Drug for Diabetes-Related Eye Disease Meets Trial Goal

Merck Says Remigromig Meets Primary Endpoint in Pivotal Brunello Trial for Diabetic Macular Edema

Merck & Co - Higher Rates of Pdr, Vitreous Hemorrhage, and Discontinuations with Remigromig

THOMSON REUTERS

Merck’s Remigromig, a Tri-Specific Agonist of the Wingless-Related Integration Site (Wnt) Pathway, Met Primary Endpoint in the Pivotal Phase 2B/3 Brunello Study of Adults with Diabetic Macular Edema

THOMSON REUTERS

Merck & Co Inc: Both Doses of Remigromig were Generally Well Tolerated

THOMSON REUTERS

Merck & Co - Both Remigromig Doses Show Non-Inferiority to Ranibizumab at 52 Weeks

THOMSON REUTERS

RBC Capital Keeps Their Hold Rating on Merck & Company (MRK)

TD Cowen Adjusts Merck Price Target to $155 From $137, Maintains Hold Rating

MT Newswires Live

Analysts Offer Insights on Healthcare Companies: Merck & Company (MRK), Celldex (CLDX) and Inventiva (IVA)

Merck & Co Inc : TD Cowen Raises Target Price to $155 from $137

THOMSON REUTERS

Wall Street Analysts Are Neutral on Top Healthcare Picks

Merck Gets FDA Label Update for WINREVAIR Based on HYPERION Trial

MT Newswires Live

Merck says FDA approves update for U.S. product label for Winrevair

U.S. FDA Approves Update to the Label for Winrevair to Include Data from the Phase 3 Hyperion Trial Evaluating Adults Recently Diagnosed with Pulmonary Arterial Hypertension

Merck Says Phase 3 Hyperion Trial Shows Winrevair Cuts PAH Clinical Worsening Risk 76%

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