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Merck & Company (MX:MRK)
:MRK
Mexico Market
EarningsQ2 2026 Earnings Report

Merck & Company (MRK) Q2 2026 Earnings Report

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MX:MRK Q2 2026 EPS Results

Actual EPS-$2.36
Consensus EPS-$4.90
Beat/MissBeat by +$2.54
One Year Ago EPS$38.68

MX:MRK Q2 2026 Revenue Results

Actual Revenue$301.10B
Expected Revenue$297.27B
Beat/MissBeat by +$3.83B
YoY Revenue Growth+4.94%

Earnings Announcement Details

QuarterQ2 2026
Date08/04/2026
TimeBefore Open
Conference CallTuesday, August 4, 2026
MX:MRK Upcoming Earnings
Merck & Company's next earnings date is estimated for October 29, 2026, based on past reporting schedules.

Q2 2026 Earnings Call Audio

MX:MRK Q2 2026 Earnings Call
0:00 / 0:00

Q2 2026 Earnings Slide Deck

Q2 2026 Earnings Call Summary

Q2 2026
Earnings Call Date:Aug 04, 2026|
% Change Since:
|
Earnings Call Sentiment|Positive
The call presented a largely positive commercial and scientific story: core revenue growth (Q2 +5%), several strong product performances (KEYTRUDA, WELIREG, WINREVAIR), meaningful vaccine and pneumococcal momentum, multiple important regulatory approvals and positive Phase III readouts (LIPFENDRA approval, sac-TMT, tulisokibart induction, islatravir combos), and raised/narrowed revenue guidance. Offsetting these positives are material one-time charges from the Terns acquisition that produced a GAAP loss and drove a volatile tax rate, margin and expense pressure, one clinical setback (SSc-ILD), and some near-term commercial headwinds (OHTUVAYRE unwind, moderating KEYTRUDA U.S. growth). Overall, management emphasized pipeline derisking, continued launches, and long-term opportunity, while acknowledging short-term impacts from the acquisition and inventory/reserve dynamics.
Company Guidance
Merck raised and narrowed its 2026 non‑GAAP guidance to $66.3–$67.3 billion in revenue (growth 2–4%, ~+1 ppt FX at mid‑July), gross margin ~81%, operating expenses $42.0–$42.7 billion (including ~$5.8 billion upfront Terns charge and MK‑4208 investment), other expense ≈$1.4 billion, and a tax rate of 35–36%; the company assumes ~2.48 billion shares outstanding and expects EPS of $2.66–$2.76 (midpoint $2.71), which includes ~+$0.15 FX benefit, a $2.31 per‑share one‑time Terns charge and ~ $0.12 per‑share ongoing MK‑4208/financing costs. Management noted Q2 revenue of $16.6 billion (up 5% / 4% ex‑FX), a Q2 loss of $0.13 per share reflecting the Terns charge, a pace of ~ $3 billion in share repurchases for 2026, and that H2 other revenue should be significantly higher due to hedging and an expected Q4 milestone, while flagging a Q3 unwind impact for OHTUVAYRE and moderating U.S. KEYTRUDA growth (no repeat of ~ $250 million wholesaler timing benefit).
Revenue Growth and Raised Guidance
Q2 total revenue of $16.6 billion, up 5% (4% ex-FX). Company raised and narrowed 2026 non-GAAP revenue guidance to $66.3B–$67.3B, representing growth of 2%–4% (including ~1 ppt FX tailwind).
KEYTRUDA Franchise Strength
KEYTRUDA family sales of $8.4 billion, up 4% year-over-year, driven by uptake in earlier-stage cancers and metastatic indications; KEYTRUDA QLEX sales $463 million with increasing adoption since permanent J-code in April.
Strong Performance from Select Oncology & Respiratory Launches
WELIREG sales grew 67% to $271 million (international launch uptake and increased U.S. use); WINREVAIR global sales grew 75% to $588 million driven by demand in pulmonary arterial hypertension; sac-TMT reported positive Phase III TroFuse-005 results with statistically significant OS and PFS improvements in certain advanced/recurrent endometrial cancer.
Vaccines and Infectious Disease Momentum
GARDASIL sales $1.2 billion, up 3% (international +6%, U.S. roughly flat); pneumococcal CAPVAXIVE sales $184 million, up 40% driven by international launches and higher U.S. demand.
HIV Pipeline and Launch Progress
Launched IDVYNSO (once-daily doravirine/islatravir) with encouraging early access/reimbursement progress; ISLEND Phase III (islatravir + lenacapavir) demonstrated maintenance of virologic suppression and supports potential first oral once-weekly HIV regimen; ongoing Phase III programs for monthly PrEP candidate alimatravir.
Major Regulatory Approval — LIPFENDRA
FDA approval of LIPFENDRA, the first oral PCSK9 inhibitor; CORALreef trial showed up to 60% LDL reduction when added to statin; additional regulatory reviews underway in EU and China.
Pipeline Derisking and Business Development
Multiple meaningful clinical and regulatory milestones materializing earlier than anticipated (sac-TMT, tulisokibart, islatravir combos), and completion of Terns acquisition to add MK-4208 and strengthen hematology pipeline, supporting management's $70B commercial opportunity thesis from >20 new products.
Animal Health and Product Diversification
Animal Health sales grew 5% (livestock +6%, companion animal +5%), demonstrating diversification beyond human pharmaceuticals and contribution from new product launches.

MX:MRK Earnings History

Report Date
Fiscal Quarter
Forecast / EPS
Last Year's EPS
EPS YoY Change
Press Release
Oct 29, 2026
2026 (Q3)
39.79 / -
46.855―
2026 (Q2)
-4.90 / -2.36
38.682-106.10% (-41.04)
2026 (Q1)
-26.77 / -23.25
40.317-157.66% (-63.56)
2025 (Q4)
36.52 / 37.05
31.23618.60% (+5.81)
2025 (Q3)
42.90 / 46.85
28.51264.33% (+18.34)
2025 (Q2)
36.92 / 38.68
41.406-6.58% (-2.72)
2025 (Q1)
38.74 / 40.32
37.5937.25% (+2.72)
2024 (Q4)
29.22 / 31.24
0.5455633.33% (+30.69)
2024 (Q3)
26.95 / 28.51
38.682-26.29% (-10.17)
2024 (Q2)
39.37 / 41.41
-37.411210.68% (+78.82)
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.
Beat
Missed