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Moderna Reports First Quarter 2026 Financial Results and Provides Business Updates

(Positive)
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Moderna (NASDAQ:MRNA) reported Q1 2026 revenue of $389 million and GAAP net loss of $(1.3) billion with GAAP EPS of $(3.40)/b, which included a non-recurring litigation settlement charge. Cash and investments were $7.5 billion as of March 31, 2026. The company reiterated a 2026 target of up to 10% revenue growth and provided full-year cost and expense frameworks, including cost of sales of approximately $1.8 billion (including the settlement).

Regulatory updates include EU approvals for mCOMBRIAX (flu + COVID), mNEXSPIKE, and mRESVIA. Moderna initiated a Phase 3 study of intismeran in high-risk Stage 1 NSCLC and expects multiple pipeline readouts in 2026.

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Positive

  • Revenue of $389 million in Q1 2026
  • EU approvals for mCOMBRIAX, mNEXSPIKE, and mRESVIA
  • Initiation of Phase 3 intismeran study in high-risk Stage 1 NSCLC
  • Q4 cash and investments of $7.5 billion as of March 31, 2026
  • 2026 target: up to 10% revenue growth

Negative

  • GAAP net loss of $(1.3 billion) in Q1 2026
  • Q1 included a $0.9 billion litigation settlement charge
  • Cost of sales expected at approximately $1.8 billion in 2026 (includes settlement)
  • Projected year-end cash $4.5–$5.0 billion for 2026

News Market Reaction – MRNA

-1.24%
30 alerts
-1.24% Session close to close
+6.9% Peak Tracked
-9.2% Trough Tracked
$18.22B Market Cap
1.4x Rel. Volume

In the May 1 session, MRNA declined 1.24%, reflecting a mild negative market reaction. Argus tracked a peak move of +6.9% during that session. Argus tracked a trough of -9.2% from its starting point during tracking. Our momentum scanner triggered 30 alerts that day, indicating elevated trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement combines Q1 2026 financials—revenue of $389M and a GAAP net loss of $(1.3)B—with i...
Analysis

This announcement combines Q1 2026 financials—revenue of $389M and a GAAP net loss of $(1.3)B—with important business updates, including EU approvals for mCOMBRIAX and mNEXSPIKE and a PDUFA date of August 5, 2026 for mRNA-1010. Investors may track execution against the 2026 framework (up to 10% revenue growth, cost controls, and year-end cash of $4.5–$5.0B) along with late-stage readouts in norovirus, oncology, and propionic acidemia to gauge how quickly the broader pipeline can offset ongoing losses.

Key Figures

Q1 2026 Revenue: $389 million International Revenue: $311 million Q1 2026 GAAP Net Loss: $(1.3) billion +5 more
8 metrics
Q1 2026 Revenue $389 million Total revenue for the first quarter of 2026
International Revenue $311 million Q1 2026 revenue from international markets
Q1 2026 GAAP Net Loss $(1.3) billion Net loss for the first quarter of 2026
Q1 2026 GAAP EPS $(3.40) Earnings per share for Q1 2026
Litigation Settlement Charge $0.9 billion Non-recurring charge impacting Q1 2026 results
Cash & Investments $7.5 billion Cash, cash equivalents and investments as of March 31, 2026
2026 Cost of Sales Outlook $1.8 billion Expected 2026 cost of sales including settlement charge
mRNA-1010 PDUFA Date August 5, 2026 FDA PDUFA goal date for seasonal flu vaccine mRNA-1010

Previous Earnings Reports

5 past events · Latest: Feb 13 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Feb 13 Q4/FY 2025 earnings Positive +5.3% Reported Q4 revenue $678M, FY 2025 revenue $1.9B and major cost cuts.
Nov 06 Q3 2025 earnings Positive +3.3% Q3 2025 revenue $1.0B, narrowed guidance and improved operating expense outlook.
Aug 01 Q2 2025 earnings Negative -6.6% Q2 2025 revenue $142M, down 41% YoY, and lowered 2025 revenue guidance.
May 01 Q1 2025 earnings Negative -5.3% Q1 2025 revenue $0.1B with $(1.0)B net loss and cost‑cut plan.
Feb 14 Q4/FY 2024 earnings Neutral +3.4% Q4 2024 revenue $1.0B, FY 2024 revenue $3.2B, large net losses but cost reductions.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings have produced mixed but often aligned reactions, with larger moves when guidance or revenue trajectory shifts notably.

Recent Company History

Across the last five earnings or financial updates from Feb 2024 through Feb 2026, Moderna repeatedly reported substantial GAAP net losses but maintained sizeable cash balances (e.g., $9.5B at 2024 year-end, $8.1B at 2025 year-end). Revenue guidance for 2025 was revised several times (e.g., to $1.5–$2.5B then $1.5–$2.2B), while operating expense cuts of roughly $2.2B annually were highlighted. Today’s Q1 2026 update, with higher revenue and ongoing cost discipline, continues this theme of managing post‑pandemic normalization while advancing a late‑stage pipeline.

Key Terms

gaap, phase 3, pdufa, adjuvant, +2 more
6 terms
gaap financial
"Reports first quarter GAAP net loss of $(1.3) billion and GAAP EPS of $(3.40)"
GAAP, or Generally Accepted Accounting Principles, are a set of standardized rules and guidelines that companies follow when preparing their financial statements. They ensure consistency, transparency, and comparability across different companies, making it easier for investors to understand and compare financial information accurately. This helps investors make informed decisions based on trustworthy and uniform financial reports.
View in glossary
phase 3 medical
"Initiated Phase 3 clinical study evaluating intismeran autogene as monotherapy"
Phase 3 is the late-stage clinical testing step for a new drug or medical treatment, where the product is given to large groups of patients to confirm effectiveness, monitor side effects, and compare it to standard care. Successful Phase 3 results are often the final scientific hurdle before regulators decide on approval and market launch—like passing a final exam before graduation—and can sharply change a company's valuation and future revenue prospects.
pdufa regulatory
"The U.S. FDA has assigned a Prescription Drug User Fee Act (PDUFA) goal date for mRNA-1010"
PDUFA is the Prescription Drug User Fee Act, the U.S. law under which drug companies pay fees that fund the FDA's review of new medicines. In company news the term usually appears as the PDUFA date, the target deadline by which the FDA aims to decide on a drug application; that date tells investors when to expect the approval or rejection decision for the product.
adjuvant medical
"Phase 3 adjuvant melanoma data, which showed a sustained benefit with intismeran"
An adjuvant is an ingredient added to a vaccine or other therapy to strengthen or shape the body’s response to the main active component, like a helper that makes the primary ingredient work better or longer. For investors, adjuvants matter because they can change how well a product performs, alter dosing and safety profiles, affect regulatory review, and therefore influence clinical success, market size and competitive advantage.
registrational medical
"The Company's PA candidate, mRNA-3927, is in a registrational study"
Used as an adjective, 'registrational' describes data, studies, or trials designed specifically to convince health regulators to approve a drug, device, or treatment. Investors care because successful registrational results are the most direct path to market authorization and revenue; think of them as the final exam or blueprint that regulators use to decide whether a product can be sold widely, so passing them can materially change a company’s value.
orphan disease medical
"Propionic acidemia (PA) therapeutic: The Company's PA candidate, mRNA-3927, is in a registrational study"
A rare medical condition that affects a very small number of people, often so few that standard drug development and commercial sales are impractical. For investors it matters because treatments for these conditions can qualify for special regulatory incentives, faster approval paths and price premiums, so a successful therapy is like owning a product that dominates a tiny but underserved niche market — high potential reward but also higher scientific and commercial risk.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Reports first quarter revenue of $0.4 billion, with approximately 80% of revenue from international markets

Reports first quarter GAAP net loss of $(1.3) billion and GAAP EPS of $(3.40), including $0.9 billion non-recurring litigation settlement charge

Reiterates plan to deliver up to 10% revenue growth and GAAP operating expense reductions in 2026, excluding the non-recurring litigation settlement charge

Advanced infectious disease portfolio with key regulatory milestones in the EU, including approval of mNEXSPIKE and mCOMBRIAX, Moderna's flu plus COVID combination vaccine

Initiated Phase 3 clinical study evaluating intismeran autogene as monotherapy and in combination with KEYTRUDA QLEX for treatment of high-risk Stage 1 non-small cell lung cancer

CAMBRIDGE, MA / ACCESS Newswire / May 1, 2026 / Moderna, Inc. (NASDAQ:MRNA) today reported financial results and provided business updates for the first quarter of 2026.

"The Moderna team delivered a great start to the year, driving significant revenue growth and substantial cost reductions building on actions taken in 2025. We received two product approvals in Europe, including the world's first flu plus COVID combination vaccine, mCOMBRIAX. We also started a new pivotal trial for intismeran-our first Phase 3 monotherapy study for high-risk Stage 1 non-small cell lung cancer patients," said Stéphane Bancel, Chief Executive Officer of Moderna. "Building on this strong first quarter momentum, we are excited to return to sales growth in 2026 and expect several additional approvals around the world, including for our seasonal flu vaccine, which would be Moderna's fifth approved product. We also look forward to important pivotal readouts this year for our norovirus, intismeran in melanoma, and propionic acidemia programs."

Commercial Updates

During the first quarter, Moderna continued to advance its multi-year revenue growth strategy by executing on strategic partnerships and key approvals. In the UK, the Company delivered the first shipment under its long-term strategic partnership. Moderna also received regulatory approval in Europe for mNEXSPIKE® and its flu plus COVID combination vaccine, mCOMBRIAX®, as well as mRESVIA® for all individuals aged 18 and older.

First Quarter 2026 Financial Results

Revenue: Total revenue for the first quarter of 2026 was $389 million, an increase of $281 million compared to the same period in 2025. Revenue was $78 million in the U.S. and $311 million in international markets. Net product sales increased due to higher COVID vaccine sales, primarily in international markets, as a result of deliveries under long-term strategic partnerships with government entities.

Cost of Sales: Cost of sales for the first quarter of 2026 was $955 million, including third-party royalties of $895 million and inventory write-downs of $38 million. Cost of sales increased by $865 million, compared to the same period in 2025, primarily driven by litigation settlement-related expenses of $878 million recognized in the first quarter of 2026 within third-party royalties. Excluding these expenses, cost of sales decreased compared to the same period in 2025, primarily due to lower unutilized manufacturing capacity costs, losses on firm purchase commitments and inventory write-downs, partially offset by higher sales volume.

Research and Development Expenses: Research and development expenses for the first quarter of 2026 were $649 million, a 24% decrease compared to the same period in 2025. The decrease was primarily driven by lower clinical development and manufacturing costs, reflecting the wind-down of large Phase 3 respiratory programs and congenital CMV studies, as well as the timing of clinical trial activities, partially offset by higher costs related to postmarketing commitments for the Company's COVID products.

Selling, General and Administrative Expenses: Selling, general and administrative expenses for the first quarter of 2026 were $173 million, an 18% decrease compared to the same period in 2025. The decrease was primarily driven by lower employee-related expenses, as well as reduced marketing costs and lower consulting and external services across multiple functions, reflecting continued discipline across the organization.

Income Taxes: Income tax provisions for both periods were not material, as the Company continues to maintain a global valuation allowance against most of its deferred tax assets.

Net Loss: Net loss was $(1.3) billion for the first quarter of 2026, compared to net loss of $(1.0) billion for the first quarter of 2025. Litigation settlement-related expenses had an unfavorable impact of $(0.9) billion on net loss for the first quarter of 2026.

Loss Per Share: Loss per share was $(3.40) for the first quarter of 2026, compared to loss per share of $(2.52) for the first quarter of 2025. Litigation settlement-related expenses had an unfavorable impact of $(2.22) on loss per share for the first quarter of 2026.

Cash Position: Cash, cash equivalents and investments as of March 31, 2026, were $7.5 billion, compared to $8.1 billion as of December 31, 2025. The decrease was primarily driven by operating losses associated with continued investment in research and development and advancement of the Company's pipeline. Litigation settlement-related expenses recognized in the first quarter of 2026 did not impact cash during the period, as the related payment of $950 million is expected to be made in the third quarter of 2026.

2026 Financial Framework

Revenue: The Company is targeting up to 10% growth from 2025 revenue and expects 2026 revenue split to be approximately 50% U.S. and approximately 50% international.

Cost of Sales: Cost of sales for 2026 is now expected to be approximately $1.8 billion, including the $0.9 billion non-recurring litigation settlement charge.

Research and Development Expenses: Research and development expenses for 2026 are anticipated to be approximately $3.0 billion.

Selling, General and Administrative Expenses: Selling, general and administrative expenses for 2026 are projected to be approximately $1.0 billion.

Income Taxes: The Company expects its full-year tax expense to be negligible.

Capital Expenditures: Capital expenditures for 2026 are expected to be $0.2 to $0.3 billion.

Cash and Investments: Year-end cash and investments for 2026 are now projected to be $4.5 to $5.0 billion, which excludes any further drawdowns from the Company's remaining $0.9 billion available under its credit facility.

Recent Progress and Upcoming Late-Stage Pipeline Milestones

Infectious disease vaccines:

  • Seasonal flu + COVID vaccine: Moderna recently presented mRNA-1083 data from a Japanese cohort at the 2026 European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Global Congress. The Company has received European Commission marketing authorization for mCOMBRIAX in the EU and its mRNA-1083 regulatory filings are under review in Canada and Australia. Moderna is awaiting further guidance from the U.S. FDA on refiling the submission for its flu plus COVID combination vaccine.

  • Seasonal flu vaccine: Moderna recently presented mRNA-1010 revaccination data at the 2026 ESCMID Global Congress. The Company's mRNA-1010 regulatory filings are under review in Europe, Canada and Australia and potential approvals are expected to begin in 2026. The U.S. FDA has assigned a Prescription Drug User Fee Act (PDUFA) goal date for mRNA-1010 of August 5, 2026.

  • Norovirus vaccine: Moderna's ongoing Phase 3 safety and efficacy study of mRNA-1403 is fully enrolled in a second Northern Hemisphere season (2025-2026) with data expected in 2026, subject to case accruals.

Oncology therapeutics:

  • Intismeran autogene: The Company is advancing mRNA-4157 in collaboration with Merck, with nine total Phase 2 and Phase 3 clinical trials underway across multiple tumor types including melanoma, non-small cell lung cancer (NSCLC), bladder cancer and renal cell carcinoma. This includes the recent initiation of a Phase 3 study of intismeran as monotherapy and in combination with KEYTRUDA QLEX for the treatment of high-risk Stage 1 NSCLC.

Fully enrolled studies include a Phase 3 adjuvant melanoma, a Phase 2 adjuvant renal cell carcinoma, and a Phase 2 adjuvant muscle invasive bladder cancer. Moderna expects Phase 3 adjuvant melanoma data potentially in 2026.

The Company recently announced an upcoming oral presentation on June 1 at 8 a.m. to 11 a.m. CT at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting highlighting positive five-year Phase 2b adjuvant melanoma data, which showed a sustained benefit with intismeran in combination with KEYTRUDA, reducing the risk of recurrence or death by 49% compared to KEYTRUDA alone.

  • mRNA-4359: Moderna's Phase 1/2 study of mRNA-4359, an investigational wholly-owned cancer antigen therapy, is ongoing. The Company recently presented mRNA-4359 data at the American Association for Cancer Research (AACR) 2026 Annual Meeting. The Phase 2 portion of the study includes cohorts in first-line metastatic melanoma, second-line+ metastatic melanoma and first-line metastatic NSCLC, and the Company expects a potential Phase 2 data readout in 2026.

Rare disease therapeutics:

  • Propionic acidemia (PA) therapeutic: The Company's PA candidate, mRNA-3927, is in a registrational study and target enrollment has been reached. Moderna expects potential data in 2026.

  • Methylmalonic acidemia (MMA) therapeutic: The Company is deferring its decision on a pivotal trial for mRNA-3705 until PA registrational data readout.

Moderna Corporate Updates

  • Entered into a settlement agreement with Arbutus Biopharma Corporation and Genevant Sciences GmbH resolving all litigation worldwide

  • Announced the initiation of Phase 3 study of mRNA-1018, Moderna's investigational pandemic influenza vaccine in collaboration with the Coalition for Epidemic Preparedness Innovations (CEPI)

Key 2026 Investor and Analyst Event Dates

  • ASCO Investor Event: June 1 at 7:15 a.m. ET

  • Science Day: June 25

  • Analyst Day: November 12

Investor Call and Webcast Information

Moderna will host a live conference call and webcast at 8:00 a.m. ET on May 1, 2026. To access the live conference call via telephone, please register at the link below. Once registered, dial-in numbers and a unique pin number will be provided. A live webcast of the call will also be available under "Events and Presentations" in the Investors section of the Moderna website.

The archived webcast will be available on Moderna's website approximately two hours after the conference call and will be available for one year following the call.

About Moderna

Moderna is a pioneer and leader in the field of mRNA medicine. Through the advancement of its technology platform, Moderna is reimagining how medicines are made to transform how we treat and prevent diseases. Since its founding, Moderna's mRNA platform has enabled the development of vaccines and therapeutics across infectious diseases, cancer, rare diseases and more.

With a global team and a unique culture, driven by the company's values and mindsets, Moderna's mission is to deliver the greatest possible impact to people through mRNA medicines. For more information about Moderna, please visit modernatx.com and connect with us on X, Facebook, Instagram, YouTube and LinkedIn.

MODERNA, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited, in millions, except per share data)

Three Months Ended March 31,

2026

2025

Revenue:
Net product sales

$

352

$

86

Other revenue1

37

22

Total revenue

389

108

Operating expenses:
Cost of sales

955

90

Research and development

649

856

Selling, general and administrative

173

212

Total operating expenses

1,777

1,158

Loss from operations

(1,388

)

(1,050

)

Interest income

72

90

Other expense, net

(18

)

(4

)

Loss before income taxes

(1,334

)

(964

)

Provision for income taxes

9

7

Net loss

$

(1,343

)

$

(971

)

Net loss per share
Basic and Diluted

$

(3.40

)

$

(2.52

)

Weighted average common shares used in calculation of net loss per share
Basic and Diluted

395

386

_______

1Includes grant, collaboration, licensing and royalty, and stand-ready manufacturing revenue.

MODERNA, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited, in millions)

March 31,

December 31,

2026

2025

Assets
Current assets:
Cash and cash equivalents

$

1,908

$

2,595

Investments

3,297

3,204

Accounts receivable, net

71

184

Inventory

146

153

Prepaid expenses and other current assets

348

408

Total current assets

5,770

6,544

Investments, non-current

2,251

2,336

Property, plant and equipment, net

2,086

2,134

Right-of-use assets, operating leases

706

719

Other non-current assets

675

605

Total assets

$

11,488

$

12,338

Liabilities and Stockholders' Equity
Current liabilities:
Accounts payable

$

161

$

317

Accrued liabilities

1,912

1,386

Deferred revenue

102

99

Other current liabilities

220

185

Total current liabilities

2,395

1,987

Deferred revenue, non-current

154

153

Operating lease liabilities, non-current

645

653

Financing lease liabilities, non-current

13

20

Long-term debt

590

590

Other non-current liabilities

283

285

Total liabilities

4,080

3,688

Stockholders' equity:
Additional paid-in capital

1,503

1,382

Accumulated other comprehensive income

25

45

Retained earnings

5,880

7,223

Total stockholders' equity

7,408

8,650

Total liabilities and stockholders' equity

$

11,488

$

12,338

MODERNA, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited, in millions)

Three Months Ended March 31,

2026

2025

Operating activities
Net loss

$

(1,343

)

$

(971

)

Adjustments to reconcile net loss to net cash used in operating activities:
Stock-based compensation

104

115

Depreciation and amortization

59

39

Amortization/accretion of investments

(11

)

(19

)

Loss on equity investments, net

2

8

Other non-cash items

6

2

Changes in assets and liabilities:
Accounts receivable, net

114

280

Prepaid expenses and other assets

54

46

Inventory

6

(8

)

Right-of-use assets, operating leases

11

9

Accounts payable

(120

)

(156

)

Accrued liabilities

464

(381

)

Deferred revenue

5

(29

)

Operating lease liabilities

(7

)

(5

)

Other liabilities

26

33

Net cash used in operating activities

(630

)

(1,037

)

Investing activities
Purchases of marketable securities

(1,348

)

(1,764

)

Proceeds from maturities of marketable securities

732

1,933

Proceeds from sales of marketable securities

602

688

Purchases of property, plant and equipment

(62

)

(117

)

Purchase of intangible asset

-

(10

)

Net cash (used in) provided by investing activities

(76

)

730

Financing activities
Proceeds from issuance of common stock through equity plans

19

3

Tax payments related to net share settlements on equity awards

(2

)

(1

)

Changes in financing lease liabilities

-

2

Net cash provided by financing activities

17

4

Effect of changes in exchange rates on cash and cash equivalents

1

-

Net decrease in cash, cash equivalents and restricted cash

(688

)

(303

)

Cash, cash equivalents and restricted cash, beginning of year

2,597

1,929

Cash, cash equivalents and restricted cash, end of period

$

1,909

$

1,626

Spikevax®, mRESVIA®, mNEXSPIKE® and mCOMBRIAX® are registered trademarks of Moderna.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including statements regarding: Moderna's 2026 financial framework, including its plan to deliver up to 10% revenue growth and GAAP operating expense reductions, and its projected year-end cash balance; Moderna's multi-year revenue growth strategy, including geographic expansion and new product launches; Moderna's continued cost discipline; Moderna's international strategic partnerships; expectations regarding mRNA-4157 Phase 3 adjuvant melanoma data in 2026; the potential of intismeran as monotherapy and in combination with KEYTRUDA QLEX; the potential of Moderna's expanded oncology portfolio; pending and anticipated regulatory filings and potential approvals, including timing of approvals; Moderna's PDUFA date in the U.S. for mRNA-1010; and anticipated progress and milestones for Moderna's pipeline programs, including potential near-term data and other catalysts. In some cases, forward-looking statements can be identified by terminology such as "will," "may," "should," "could," "expects," "intends," "plans," "aims," "anticipates," "believes," "estimates," "predicts," "potential," "continue," or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. The forward-looking statements in this press release are neither promises nor guarantees, and you should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties, and other factors, many of which are beyond Moderna's control and which could cause actual results to differ materially from those expressed or implied by these forward-looking statements. These risks, uncertainties, and other factors include, among others, those risks and uncertainties described under the heading "Risk Factors" in Moderna's Annual Report on Form 10-K for the fiscal year ended December 31, 2025, filed with the U.S. Securities and Exchange Commission (SEC), and in subsequent filings made by Moderna with the SEC, which are available on the SEC's website at www.sec.gov. Except as required by law, Moderna disclaims any intention or responsibility for updating or revising any forward-looking statements contained in this press release in the event of new information, future developments or otherwise. These forward-looking statements are based on Moderna's current expectations and speak only as of the date of this press release.

###

Moderna Contacts

Media:
Chris Ridley
Vice President, Head of Global Communications
+1 617-800-3651
Chris.Ridley@modernatx.com

Investors:
Lavina Talukdar
Senior Vice President & Head of Investor Relations
+1 617-209-5834
Lavina.Talukdar@modernatx.com

SOURCE: Moderna, Inc.



View the original press release on ACCESS Newswire

FAQ

What were Moderna's (MRNA) Q1 2026 revenue and GAAP EPS?

Moderna reported Q1 2026 revenue of $389 million and GAAP EPS of $(3.40). According to the company, the quarter included a $0.9 billion non-recurring litigation settlement that materially affected GAAP results.

How did the $0.9 billion litigation settlement affect Moderna's Q1 2026 results?

The $0.9 billion settlement increased Q1 cost and lowered net income, contributing to a $(1.3 billion) GAAP net loss. According to the company, the cash payment is expected in Q3 2026 and did not reduce Q1 cash balance.

What regulatory approvals did Moderna (MRNA) announce in May 2026?

Moderna announced EU approvals for mCOMBRIAX (flu + COVID), mNEXSPIKE, and mRESVIA. According to the company, mCOMBRIAX is the first approved flu plus COVID combination vaccine in Europe.

What is Moderna's 2026 financial outlook for revenue and cash (MRNA)?

Moderna targets up to 10% revenue growth for 2026 and projects year-end cash and investments of $4.5–$5.0 billion. According to the company, projections exclude additional drawdowns under its credit facility.

What pipeline milestones and late-stage trials did Moderna (MRNA) highlight for 2026?

Moderna initiated a Phase 3 intismeran study in high-risk Stage 1 NSCLC and expects key readouts for norovirus, melanoma, and propionic acidemia in 2026. According to the company, multiple pivotal data points are anticipated this year.