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    PFE
    Earnings call· Jun 2026(Q2 FY26)

    PFIZER Q2 FY26 earnings call PFE

    Aug 4, 2026 Source

    Executive summary

    Pfizer Inc. Q2 FY26 — Strong Non-COVID Performance and Raised Revenue Guidance

    Pfizer delivered a strong Q2 FY26, driven by robust performance in its non-COVID portfolio and acquired assets, leading to a raise in full-year revenue guidance despite lower COVID-19 product sales. The company continues to advance a deep R&D pipeline, particularly in oncology and obesity, while expanding cost-saving initiatives and reaffirming its commitment to dividend growth post-LOE period. Strategic investments in AI are also accelerating productivity across the business.

    Highlights

    5
    • Q2 FY26 revenues of $15 billion exceeded expectations, representing a 1% operational increase year-over-year.

    • Excluding COVID products, the underlying business delivered 5% operational revenue growth.

    • Launched and acquired products delivered $3.2 billion in revenue, growing 18% operationally (27% excluding prior year one-time impact).

    • Adjusted diluted EPS of $0.77 exceeded expectations, reflecting cost discipline and strong non-COVID revenue.

    • Midpoint of full-year 2026 revenue guidance raised by $500 million to $60.5 billion - $62.5 billion.

    Concerns

    5
    • Lower-than-expected COVID revenues, with full-year 2026 COVID-19 revenue expectations revised down to $4 billion from $5 billion.

    • Q2 GAAP results included a $4.3 billion noncash intangible asset impairment due to SV Phase III readout failure and Oxbryta revenue forecast removal.

    • Adjusted diluted EPS guidance of $2.80 - $3.00 now absorbs an unfavorable $0.10 impact from the Innovent Biologics transaction's Acquired IPR&D charge.

    • Leverage ended the quarter at 2.7x and is expected to remain around current or modestly higher levels through the LOE transition period.

    • Phase III trial for sigvotatug vedotin (SV) in non-small cell lung cancer did not meet its primary overall survival endpoint.

    Guidance & targets

    10
    CategoryTargetConfidence
    Full-year 2026 Revenue
    $60.5 billion - $62.5 billion
    high materiality
    High
    Full-year 2026 Adjusted Diluted EPS
    $2.80 - $3.00
    high materiality
    High
    COVID-19 Revenues
    approximately $4 billion
    medium materiality
    Medium
    Net Cost Savings (Productivity Enhancement)
    $6.7 billion
    medium materiality
    High
    Net Cost Savings (Manufacturing Optimization)
    $3 billion
    medium materiality
    High
    Total Net Cost Savings
    $9.7 billion
    high materiality
    High
    First Approval for Berobenatide
    2028
    high materiality
    Medium
    Revenue CAGR
    high single-digit
    high materiality
    High
    Dividend Policy
    maintain and over time, grow
    high materiality
    High
    Adjusted Gross Margin
    mid-70s range
    medium materiality
    High

    Segment performance

    5
    SegmentRevenueYoYQoQMargin
    Total Company (excluding COVID products)
    Operational revenue growth for the underlying business, excluding COVID products.
    5%
    Launched and Acquired Products
    Strong contribution from key brands and recent acquisitions.
    Operational growth (excluding one-time impact in Q2 2025): 27%
    $3.2 billion18%
    Legacy Seagen Portfolio (U.S.)
    Year-over-year increase, excluding one-time stocking benefit in Q2 2025.
    21%
    Padcev
    Strong growth driven by commercial execution and label expansion across bladder cancer continuum.
    LAM UC new patient share: above 60%
    over 20%
    Nurtec
    Continued strong year-over-year growth and market leadership.
    Leadership in oral CGRP class: Total Prescriptions
    strong

    Operational metrics

    11
    Adjusted Gross Margin
    76%
    Q2 FY26
    Adjusted Operating Expenses
    $6.1 billionincreased 4% operationally YoY
    Q2 FY26
    Adjusted Operating Margin
    35%
    Q2 FY26
    Leverage Ratio
    2.7x
    Q2 FY26

    Ended the quarter at this level, expected to remain around current or modestly higher through LOE transition.

    Acquired In-Process R&D Expense
    $650 million
    Q3 FY26

    Initial upfront payment to be recorded in Q3.

    Intangible Asset Impairments
    $4.3 billion
    Q2 FY26
    Dividend Returned to Shareholders
    $4.9 billion
    H1 FY26

    Via quarterly dividend.

    TCJA Repatriation Tax Payment
    $2.6 billion
    Q2 FY26

    Final payment made earlier in the quarter.

    Net Cash Proceeds from ViiV Exit
    $1.65 billion
    Q2 FY26

    Closed on exit of ViiV.

    BD Capacity
    $6 billion
    Q2 FY26

    Remaining business development capacity following the Innovent Biologics transaction.

    Investment in Internal and External R&D
    $5.5 billion
    H1 FY26

    Industry KPIs

    11
    MetricValueDetails
    Prescription volumeleadership
    EPS revenue guidanceRevenue: $60.5B-$62.5B; Adj. EPS: $2.80-$3.00USD
    Pricing policy impactCMS proposal to cut reimbursement for 340B hospital payments
    Product franchise net sales$3.2 billionUSD
    Pipeline clinical milestones8 pivotal study startscount
    Regulatory approvals filings3count
    Therapeutic drug market shareabove 60%%
    Glp 1 incretin franchise metricsup to 12.3%%
    Geographic regional revenue growth5%%
    Clinical trial efficacy safety data19.5%%
    Business development capacity deal appetite$6 billionUSD

    Deals & partnerships

    5
    SeagenAcquisition of an innovative platform, deep scientific expertise, and a promising ADC pipeline.

    Central to goal of growing Oncology leadership.

    MetseraAcquisition to unlock a differentiated profile for patients with obesity and related conditions.

    Berobenatide, an investigational ultra-long-acting GLP-1 receptor agonist, is targeting first approval in 2028.

    BiohavenAcquisition positioned Pfizer as a leader in migraine treatment options.

    Migraine affects an estimated 1.2 billion people worldwide.

    Innovent BiologicsTransaction resulting in an Acquired In-Process R&D expense.$650 million

    Deal closed in July.

    ViiVExit from ViiV.

    Closed earlier in the quarter.

    Risks & headwinds

    7
    Lower-than-expected COVID-19 revenuesFY26

    Revised down to $4 billion from $5 billion for FY26

    Mitigation: Strong performance of non-COVID portfolio and cost discipline have offset the shortfall.

    Unfavorable impact from Innovent Biologics transactionFY26

    Approximately $0.10 impact on adjusted diluted EPS

    Mitigation: Absorbed within the reaffirmed EPS guidance range.

    Intangible asset impairmentsQ2 FY26

    $4.3 billion noncash charge

    Mitigation: Resulted from SV Phase III readout failure and removal of Oxbryta revenue projections. SV still has risk-adjusted revenue forecast in other indications.

    Leverage remaining elevatedthrough LOE transition period

    Ended Q2 at 2.7x, expected to remain around current or modestly higher

    Mitigation: Disciplined capital allocation and focus on long-term growth and dividend maintenance.

    Low COVID-19 incidenceongoing

    Could continue to limit Paxlovid utilization

    Mitigation: Comirnaty sales expected towards year-end consistent with vaccination season; non-COVID business offsetting impact.

    Currency fluctuationongoing

    Not quantified

    Mitigation: Will continue to monitor as the year progresses.

    340B hospital payments proposal

    CMS proposal to cut reimbursement from ASP +6% to ASP -33%

    Mitigation: Pfizer is actively explaining the program's deviation from original intent to regulators and legislators; outcome uncertain.

    What to watch in Q3 FY26

    5

    Mivrometostat MEVPRO-1 data readout

    Q4
    CurrentTrial fully enrolled, events not yet reached
    TargetFirst readout expected

    Why it matters

    This is a potential breakthrough therapy in prostate cancer, and the readout will validate the mechanism and commercial opportunity.

    MEVPRO-1, our goal is to delay resistance to Xtandi, which has historically delivered radiographic progression-free survival of about 5 to 8 months in similar settings. Each of these studies is event-driven with the first readout expected in the fourth quarter based on the current event rate.

    Q&A highlights

    6

    What defines success for the MEVPRO-1 trial, specifically regarding the magnitude of benefit and its implications for broad adoption?

    The trial is event-driven and fully enrolled, with events not yet reached. Success is defined by a clinically meaningful benefit of approximately 30% over standard of care, based on a hazard ratio. The control arm is expected to perform at 5-8 months PFS. The Phase I data showed a hazard ratio of 0.5, doubling radiographic PFS.

    MEVPRO-1, 2 and 3 are event-driven studies, meaning control and experimental arm is where events could happen. However, the statistical analysis plan is based on a clinically meaningful benefit of approximately 30% over standard of care because that will be clinically meaningful. And it's hazard ratio based.

    asked by Evan Seigerman · answered by Chris Boshoff

    2 min read6 chapters

    Detailed Narrative

    01

    Strategic Priorities and Acquisitions Driving Growth

    Pfizer's strategic priorities are centered on maximizing value from key transactions like Seagen, Metsera, and Biohaven. Acquired products saw 25% operational revenue growth, excluding one-time items📎. The legacy Seagen portfolio in the U.S. grew 21% year-over-year, exceeding initial expectations. Metsera's berobenatide, an ultra-long-acting GLP-1, is targeting a first approval in 2028 with 10 Phase III studies planned this year. Biohaven's Nurtec continues to lead the oral CGRP class in prescriptions, with ongoing Phase III trials for menstrual and chronic migraine.

    02

    Pipeline Progress and R&D Focus

    The R&D pipeline achieved 3 regulatory approvals, 6 key data readouts, and 8 pivotal study starts in the first half of the year. Oncology is a key strength, with a dozen late-stage studies initiated and 6 regulatory approvals in the past two years. Key assets like Padcev received expanded FDA approval for muscle-invasive bladder cancer, and mivrometostat, an EZH2 inhibitor, is in Phase III for prostate cancer with a readout expected in Q4. The company is also advancing next-wave ADC breakthroughs and a PD-1 x VEGF bispecific antibody, 4404, with promising early data.

    03

    Cost Optimization and Financial Discipline

    Pfizer is expanding its cost improvement programs, now expecting approximately $9.7 billion in total net cost savings through 2029. This includes $6.7 billion from productivity enhancement (up $1 billion) and $3 billion from manufacturing optimization (up $1.5 billion). These initiatives are designed to enhance operating efficiency, support margin expansion, and enable continued investment in innovation. Adjusted gross margin for Q2 was 76%, reflecting product mix and cost control.

    04

    AI Integration for R&D and Commercial Effectiveness

    AI is viewed as a structural transformation opportunity to accelerate R&D, improve productivity, and enhance competitive positioning. The company is already seeing benefits in manufacturing cost reduction and yield expansion, as well as increased effectiveness of its commercial field force and marketing. The ambition is to build an AI-native R&D organization, continuously informing decisions from target discovery through medical evidence.

    05

    Capital Allocation and Shareholder Returns

    The capital allocation strategy focuses on reinvesting in the business, maintaining and growing the dividend over time, and preserving optionality for future value-enhancing actions like share repurchases. In H1 2026, $5.5 billion was invested in R&D, and $4.9 billion was returned to shareholders via dividends. The company has approximately $6 billion in remaining business development capacity, with a focus on bolt-on acquisitions in oncology, immune-inflammation, primary care (obesity), and vaccines.

    06

    COVID-19 Business Performance and Outlook

    Q2 FY26 COVID-19 revenues were lower than expected due to low infection levels, primarily impacting Paxlovid. Full-year COVID-19 revenue guidance was revised down to $4 billion from $5 billion. Comirnaty sales are expected to occur mostly towards year-end, consistent with vaccination season. The company emphasizes that the non-COVID business's strong performance has offset the shortfall from COVID products this year.

    AI-generated summary of the company’s earnings call. Not investment advice.