Ticker reaction data · Healthcare

Merck & Company, Inc. (new) (MRK)

MRK moved a median of +0.02% 30 minutes after news, and +0.14% by the close. How MRK actually reacts to news — the realized, point-in-time move the market made, measured across 1,319 labeled events over the last three years with zero look-ahead.

The quantified answer

MRK’s median reaction, across the day.

+0.02%
Median 30-min
Typical reaction 30 minutes after any MRK news
51%
Moved up
Share of MRK news events that rose at 30 minutes
+0.14%
Median to close
Where MRK typically settles by the closing bell
MRK median reaction to newsMRK median reaction to news across 4 horizons: 5-min -0.01%, 30-min +0.02%, 60-min +0.01%, to close +0.14%.5-min30-min60-minto close5-min: -0.01%30-min: +0.02%60-min: +0.01%to close: +0.14%-0.01%+0.02%+0.01%+0.14%-0.01%0+0.14%
Median move vs. the price at the news timestamp, each horizon on its own sample — the counts are in the table below.
MRK median reaction to news, by horizon. Each rung is measured on the events that traded at that horizon.
HorizonMedian% positiveEvents
5-min-0.01%47%1,318
30-min+0.02%51%1,319
60-min+0.01%50%1,319
to close+0.14%54%1,307
Where MRK reactions landvs 1,319 measured MRK reactions
MRKMiddle 50% · -0.41% to +0.55%Zero: 0.00%Median: +0.02%Median +0.02%-1.00%0+1.00%
Middle 50% of MRK reactions-0.41% to +0.55%
Median reaction (30-min)+0.02%
Measured reactions1,319
Point-in-time · zero look-ahead

Half of all Merck & Company, Inc. (new) news events land between -0.41% and +0.55% at 30 minutes.

Reaction stats as of 2026-09-21. Newest measured event . Reaction = percent move vs. the price at the news timestamp.

By event type

How MRK reacts, by analyst action.

EventEventsMedian 30-min% positiveMedian to close
Analyst upgrades39+0.36%67%+0.31%
Analyst downgrades35-0.09%40%-0.87%
Coverage initiations28+0.01%50%-0.17%
Rating reiterations126+0.06%56%-0.04%
Price-target raises47+0.07%62%-0.08%
Price-target cuts26-0.16%39%-0.20%

Last 3 years, pulled 2026-09-21. Reaction = percent move vs. the price at the news timestamp. Counts and medians only. The same measurement runs across every name in the dataset. See how MRK ranks against every other measured name →

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26M+ news records Operating since 2012 Methodology on SSRN ↗
Latest news

Recent MRK events, each with its measured reaction.

DateHeadlineEventSource5-minTo close
Form 8-K Merck & Co., Inc. For: Oct 09SEC filing · Form 8-KSEC EDGAR+0.24%-0.43%
Merck Showcases First-Time Pivotal Phase 3 Results From Oncology Pipeline and Continued Innovative Potential of Existing Portfolio at ESMO 2026Press releaseBusiness Wire-0.09%-2.65%
Paul J. Diaz Elected to Merck & Co., Inc., Rahway, N.J., USA Board of DirectorsPress releaseBusiness Wire-0.09%-2.65%
Merck Presents One-Year Results from the Pivotal Phase 2b/3 BRUNELLO Study Evaluating Remigromig, a Tri-specific Agonist of the Wingless-related Integration Site (Wnt) Pathway, in Adults with Diabetic Macular Edema at AAO 2026Press releaseBusiness Wire+0.43%+0.08%
Merck to Hold Third-Quarter 2026 Sales and Earnings Conference Call Oct. 29Press releaseBusiness Wire-0.14%-0.62%
Merck's Tulisokibart Met Primary and Key Secondary Endpoints in Phase 2b Study in Patients With Moderate to Severe Hidradenitis Suppurativa (HS)Press releaseBusiness Wire-0.40%-2.56%
CAPVAXIVE® Included in Ontario's Publicly Funded Adult Pneumococcal Immunization ProgramPress releaseCanada Newswire+0.62%+0.70%
Merck Enters into Exclusive Global License Agreement with SciBrunch Therapeutics for SPR2015, an Investigational Oral KRAS G12D (ON) InhibitorPress releaseBusiness Wire+0.62%+0.70%
Ifinatamab Deruxtecan Biologics License Application for Certain Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily WithdrawnPress releaseBusiness Wire+0.62%+0.70%
U.S. FDA Approves WELIREG® (belzutifan) Plus LENVIMA® (lenvatinib) for Certain Previously Treated Adult Patients With Advanced Renal Cell Carcinoma With a Clear Cell Component (ccRCC)Press releaseBusiness Wire+0.82%+0.49%
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 EdemaPress releaseBusiness Wire+1.18%-0.02%
U.S. FDA Approves Update to the Label for WINREVAIR™ (sotatercept-csrk) to Include Data from the Phase 3 HYPERION Trial Evaluating Adults Recently Diagnosed with Pulmonary Arterial Hypertension (PAH, WHO* Group 1 Pulmonary Hypertension)Press releaseBusiness Wire-0.09%+1.49%
Merck Canada Partners with the Montreal Museum of Fine Arts to Present the North American Premiere of Chiharu Shiota: The Soul TremblesPress releaseCanada Newswire+0.83%+2.24%
Merck’s KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph) Approved in Japan for Subcutaneous Administration for All KEYTRUDA® (pembrolizumab) Indications Approved in JapanPress releaseBusiness Wire+0.83%+2.24%
Merck Launches Your Hive of Whole Health to Support Whole Person Care for People Living With HIVPress releaseBusiness Wire+0.48%-0.08%
Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) as Perioperative Treatment for Adults With Resectable Muscle-Invasive Bladder Cancer (MIBC)Press releaseBusiness Wire+0.48%-0.08%
Merck to Participate in the Morgan Stanley 24th Annual Global Healthcare ConferencePress releaseBusiness Wire-1.05%+0.03%
Merck to Participate in the Wells Fargo 21st Annual Healthcare ConferencePress releaseBusiness Wire+1.07%+0.65%
Merck and Moderna Announce Phase 3 INTerpath-001 Trial of Intismeran Autogene Plus KEYTRUDA® Met Endpoints of Recurrence-Free Survival (RFS) and Distant Metastasis-Free Survival (DMFS) in Patients With Completely Resected Stage IIB-IV MelanomaPress releaseBusiness Wire+0.11%+3.48%
Form 10-Q Merck & Co., Inc. For: Jun 30SEC filing · Form 10-QSEC EDGAR+0.77%—
Form 13F-HR Merck & Co., Inc. For: Jun 30SEC filing · Form 13F-HRSEC EDGAR+0.77%—
U.S. FDA Accepts sBLA for ENFLONSIA™ (clesrovimab-cfor) to Update its Respiratory Syncytial Virus (RSV) Lower Respiratory Tract Disease Indication to Include Children Under Two Years at Increased Risk for Severe RSV for Their Second SeasonPress releaseBusiness Wire-0.73%-1.98%
Health Canada Approves KEYTRUDA® for the treatment of adult patients with muscle invasive bladder cancer who are ineligible for cisplatin containing chemotherapy, in combination with enfortumab vedotin, as neoadjuvant treatment and then continued after raPress releaseCanada Newswire+0.03%-1.79%
Form 8-K Merck & Co., Inc. For: Aug 04SEC filing · Form 8-KSEC EDGAR-2.21%-0.94%
Merck & Co., Inc., Rahway, N.J., USA Announces Second-Quarter 2026 Financial Results; Highlights Key Regulatory and Clinical Milestones Across Broad, Diverse PipelinePress releaseBusiness Wire-2.21%-0.94%
Merck Announces Fourth-Quarter 2026 DividendPress releaseBusiness Wire+0.35%-0.10%
Merck Announces Initial Access Plans for Alimatravir, an Investigational Once-Monthly Oral HIV Pre-Exposure Prophylaxis in Phase 3 DevelopmentPress releaseBusiness Wire-0.15%+0.12%
Tessera Therapeutics Appoints Joseph Romanelli as President and Chief Executive OfficerPress releasePR Newswire-0.00%+0.35%
Merck’s LIPFENDRA® (enlicitide) is the First and Only Once-Daily Oral PCSK9 Inhibitor Approved by the U.S. FDA to Reduce LDL-C in Adults with HypercholesterolemiaPress releaseBusiness Wire+1.38%+2.66%
KEYTRUDA® (pembrolizumab) as Monotherapy Significantly Improved Progression-Free Survival (PFS) in Certain Patients With Advanced or Recurrent Endometrial Cancer With Mismatch Repair Deficient (dMMR) Tumors Compared to ChemotherapyPress releaseBusiness Wire-0.09%-0.14%
Merck to Present New Data on Daily, Weekly, and Monthly Options Across its HIV Treatment and Prevention Pipeline at AIDS 2026Press releaseBusiness Wire-0.09%-0.14%
FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With Padcev® (enfortumab vedotin-ejfv), as Treatment Before and After Surgery for Adults With Muscle-Invasive Bladder Cancer (MIBC)Press releaseBusiness Wire-0.01%+0.22%
Merck to Hold Second-Quarter 2026 Sales and Earnings Conference Call Aug. 4Press releaseBusiness Wire-0.66%-2.06%
Merck Announces New Agreement with ADAP Crisis Task Force to Improve Access and Care for People Living with HIVPress releaseBusiness Wire-0.41%+1.32%
FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), each with Trodelvy® (sacituzumab govitecan-hziy) as First-Line Treatment of PD-L1+ (CPS =10) Advanced Triple-Negative Breast Cancer (TNBC)Press releaseBusiness Wire+0.40%+2.95%
European Commission Approves KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) as First PD-1 Inhibitor Plus Antibody-Drug Conjugate Regimen for Adults With Cisplatin-Ineligible Resectable Muscle-Invasive Bladder CancerPress releaseBusiness Wire-0.18%-0.73%
Form 11-K Merck & Co., Inc. For: Dec 31SEC filing · Form 11-KSEC EDGAR+0.09%-0.54%
Next-Generation DNA Repair Inhibitors Could Capture Billions in Emerging MarketPress releaseGlobeNewswire-0.18%-0.73%
Merck’s Tulisokibart Met Primary and Key Secondary Endpoints in the Phase 3 ATLAS-UC Induction-only Study in Patients With Moderately to Severely Active Ulcerative Colitis (UC)Press releaseBusiness Wire-0.24%+1.04%
U.S. FDA Approves an Additional Indication for CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) in Children and Adolescents Aged 2 through 17 at Increased Risk for Pneumococcal DiseasePress releaseBusiness Wire-0.57%-0.58%
Study Reveals Dog Owners and Veterinarians See Challenges in Treating Allergic Skin Disease, Highlighting a Need for a Targeted Rapid Onset Treatment for Dogs of All AgesPress releaseBusiness Wire+0.06%+0.82%
FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With WELIREG® (belzutifan), for Adjuvant Treatment of Certain Patients With Clear Cell Renal Cell Carcinoma (ccRCC)Press releaseBusiness Wire-2.22%-2.39%
Merck Animal Health to Acquire TARGANPress releaseBusiness Wire-0.08%+0.39%
PDA Announces Glenn E. Wright is Stepping Down as CEO & President on June 30, 2026; Craig Elliott Assuming Role Effective July 1, 2026Press releasePR Web+0.03%-0.37%
Merck and Gilead Provide Update on Phase 3 KEYNOTE-D46/EVOKE-03 StudyPress releaseBusiness Wire-0.62%-0.26%
Apotex launches sitagliptin tablets and sitagliptin and metformin hydrochloride tablets, eligible for 180-day shared exclusivityPress releaseCanada Newswire+0.76%-0.78%
Merck to Participate in the Goldman Sachs 47th Annual Global Healthcare ConferencePress releaseBusiness Wire+0.95%+0.76%
FDA Grants Breakthrough Therapy Designation for Calderasib (MK-1084), an Investigational KRAS G12C Inhibitor, for Certain Patients with Newly Diagnosed Metastatic KRAS G12C-Mutant Non-Small Cell Lung Cancer (NSCLC)Press releaseBusiness Wire+0.17%-1.01%
Form SD Merck & Co., Inc.SEC filing · Form SDSEC EDGAR+0.01%-0.08%
Form 8-K Merck & Co., Inc. For: May 26SEC filing · Form 8-KSEC EDGAR+0.17%-1.01%

Each reaction is the move the market actually made, measured from the news timestamp. Headlines link through to the MRK section they belong to.

Keep exploring

Where else MRK is measured.

MRK earnings → · Analyst actions → · SEC filings →

Other Healthcare names, measured the same way

TickerEventsMedian 30-min% positive
MOMENTA PHARMACEUTICALS (MNTA)1,3550.00%46%
Clovis Oncology, Inc. (CLVS)1,349-0.20%47%
Humana Inc. (HUM)1,306+0.02%51%
WELLCARE HEALTH PLANS (WCG)1,2920.00%50%

Same sector, same measurement: percent move vs. the price at the news timestamp, read at 30 minutes. Sample sizes differ, so the medians are comparable but the confidence behind them is not.

All Healthcare names, measured the same way →

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Every name we’ve measured, in one place.

Method

How the numbers are made.

How is Merck & Company, Inc. (new)'s median reaction calculated?

Every labeled MRK news event is measured from its own timestamp: the last trade before the news is the base price, and the move is read at fixed horizons — 30 minutes of trading, then the close. The median across 1,319 events is what this page reports. Point-in-time, zero look-ahead: no event borrows information from a later one.

What counts as a positive reaction?

Any event whose price move is above zero at the horizon, relative to the last trade before the news timestamp. 51% of MRK's measured events are up at 30 minutes; the rest close the window flat or negative.

How often is this page updated?

The news table refreshes automatically as new events are labeled and priced. The reaction medians are re-pulled in batches from the dataset — the figures here are as of 2026-09-21.

Does MRK's past reaction predict its next one?

No. These are realized facts about past events, not forecasts. They describe a distribution — they say nothing certain about any future move.

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26M+ news records, 2006–2026 Operating since 2012 Point-in-time, zero look-ahead Peer-reviewable methodology (SSRN) ↗