Merck & Co. 10-Qquarter ended 2026-03-31

MixedRestructuringImpairment / charge

Cidara’s influenza-pipeline acquisition drove a GAAP loss despite sales growth led by Keytruda and Winrevair.

Filed 2026-05-04 16:10 ET

Key figures · Q1 FY2026 · period ended 2026-03-31

  • Revenue$16.3BYoY +4.9%QoQ −0.7%
  • Operating income— Not reported
  • Net income−$4.2BYear ago $5.1BPrevious quarter $3.0B
  • Total assets$128.7BYoY +11.8%QoQ −6.0%
  • Total debt
    How total debt adds up
    Long-Term Debt$46,673M
    + Loans payable and current portion of long-term debt$2,444M
    Total debt$49,117M

    Lines as the filer presents them on its balance sheet.

    $49.1B1YoY +41.0%QoQ −0.4%
  • Shareholders' equity$45.9BYoY −5.1%QoQ −12.8%
  • Tangible book value−$1.4BYear ago $10.9BPrevious quarter $4.3B
Notes (1)
  1. Total debt: About the summary: The summary's $46.7B is the Long-Term Debt line, one of the 2 lines that make up total debt (see ⓘ).

How this filing reads

  • Health+0.2Operating cash flow was $3.92B and free cash flow $2.93B against $46.7B long-term debt.
  • Momentum+0.3Sales rose 5% year over year, while gross margin declined to 74.2% from 78.0%.
  • Outlook−0.4Nearly all U.S. Januvia and Janumet sales are expected to disappear after May 2026.
  • Restructuring“Q1 charges were $466M, and its broader multiyear initiative targets $3.0B in annual savings for reinvestment.”
  • Impairment / charge“Its $4.24B GAAP loss reflects a $9.0B charge for acquiring Cidara’s influenza-prevention candidate”

Executive Summary

Merck grew Q1 2026 sales 5% as Keytruda, Winrevair and Animal Health more than offset declines in Gardasil and older medicines. Its $4.24B GAAP loss reflects a $9.0B charge for acquiring Cidara’s influenza-prevention candidate, rather than a collapse in product demand; operating cash flow remained positive. The acquisition reduced cash and equity, while a planned Terns purchase would add another large R&D charge and require financing. For investors, the question is whether Merck’s expanding pipeline and newer products can outweigh Keytruda concentration, vaccine weakness and imminent generic competition.

Key Financial Highlights

Metric Q1 2026 / 3/31/2026 Investor interpretation
Revenue $16.3B, +5% Y/Y Growth was 3% excluding foreign exchange.
Gross profit; gross margin $12.1B; 74.2% vs 78.0% Acquired-intangible amortization and inventory accounting compressed margin.
GAAP net loss; diluted EPS $(4.24)B; $(1.72), vs $5.08B income; $2.01 The Cidara R&D charge dominated reported earnings.
R&D expense $12.6B vs $3.62B Includes the $9.0B Cidara charge.
OCF; FCF $3.92B; $2.93B Cash flow and earnings diverged largely because the acquisition charge was added back in OCF.
Total assets; total equity $129B; $45.9B, vs $137B; $52.7B at year-end Acquisition spending and the reported loss reduced the balance sheet.
Tangible common equity $(1.40)B Equity less $21.6B of goodwill and $25.7B of other intangible assets, net.
Cash and equivalents; long-term debt $5.33B vs $14.6B at year-end; $46.7B Cidara materially reduced immediately available cash.
  • Revenue mix: Pharmaceuticals generated $14.3B; Animal Health generated $1.79B, up 13% reported but 6% excluding foreign exchange. Keytruda and Keytruda Qlex together generated $8.03B, up 12%, making growth increasingly dependent on that franchise.
  • Cash conversion: OCF included an $8.54B add-back for R&D asset-acquisition charges. Investing cash outflow included $8.78B of net cash paid for Cidara; capital expenditures were $991M.
  • Capital return: Dividends paid were $2.11B. Cash-flow reporting shows $874M of repurchases, while the equity activity disclosure shows $925M of treasury-stock purchases; net shares outstanding fell by ≈4.9M, from ≈2.475B to ≈2.470B.
  • Financing and tax: Interest expense rose to $479M from $313M. A $709M tax provision despite a pretax loss produced a (20.1)% effective tax rate, principally because the Cidara charge yielded no tax benefit.

Business Developments

Oncology remains Merck’s principal commercial engine, but Q1 Keytruda growth included ≈$250M of favorable U.S. wholesaler-purchase timing. Winrevair sales reached $525M, up 88%, while Animal Health benefited from livestock and companion-animal demand. In contrast, Gardasil/Gardasil 9 sales fell 19% to $1.07B; China shipments have been suspended since February 2025, and Merck expects any 2026 shipments there to be immaterial. These trends shift the near-term growth burden toward oncology and newer cardiopulmonary products.

Merck acquired Cidara for $9.2B, gaining Phase 3 influenza-prevention candidate MK-1406. It also agreed to buy Terns for ≈$6.7B to add investigational leukemia treatment TERN-701; closing is expected to produce an ≈$5.8B R&D charge. These deals are pipeline investments, not contributions that offset their near-term earnings and financing costs.

Management is restructuring to fund growth: Q1 charges were $466M, and its broader multiyear initiative targets $3.0B in annual savings for reinvestment. Pipeline progress includes an October 2026 regulatory decision date for antibody-drug conjugate I-DXd, but failures in two Keytruda trials and one Welireg trial show that additional indications cannot be assumed.

Risk Assessment

  • Keytruda concentration: Keytruda and Keytruda Qlex generated $8.03B, nearly half of sales; reimbursement, future negotiated U.S. pricing and eventual biosimilar competition therefore have outsized consequences.
  • Patent expirations and pricing: U.S. generic entry for Januvia and Janumet begins in May 2026, followed by Bridion exclusivity expiration in July; Merck expects to lose nearly all U.S. Januvia and Janumet sales after May.
  • Gardasil demand: Sales fell 19%, China shipments remain suspended, and uncertainty around vaccine recommendations and purchasing could delay recovery.
  • Acquisition funding and execution: Cash and equivalents fell to $5.33B; Merck arranged a delayed-draw term loan of up to $6.0B for Terns and intends to refinance it with long-term debt, increasing exposure if pipeline returns disappoint.
  • Clinical development: Recent unsuccessful oncology trials and the decision to discontinue MK-1308A underscore the risk that R&D spending does not yield approvals or sales.
  • Legal and tax: Product-liability litigation includes ≈135 U.S. Gardasil cases and ≈735 talc-related cases; the IRS separately proposes ≈$1.3B of additional transition tax and $260M of penalties, excluding interest, which Merck contests.

A 10-Q does not have to restate the risk factors in the annual report. Full list: FY2025 10-K.

Strategic Outlook and Investor Actionables

Merck is using cash, acquisitions and restructuring to build growth beyond mature products. The strategy has visible new-product momentum, but upcoming patent losses and acquisition charges will obscure near-term earnings and test whether pipeline investment creates durable revenue.

  • Monitor Keytruda and Keytruda Qlex growth excluding wholesaler timing, alongside Winrevair sales: sustained demand would support the growth thesis beyond Q1’s purchase-timing benefit.
  • Monitor Gardasil China shipments and U.S. Januvia/Janumet sales after May: continued vaccine weakness plus rapid generic erosion would increase dependence on newer launches.
  • Monitor the Terns closing, associated R&D charge, financing and OCF: pipeline progress must justify the additional balance-sheet commitment.

Figures are computed from the filing's XBRL data; the summary and scores are written by an AI model reading the filing.

Model 005 · prompt 9e47f58d3c

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