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Moderna (MRNA)
NASDAQ:MRNA

Moderna (MRNA) AI Stock Analysis

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MRNA

Moderna

(NASDAQ:MRNA)

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Neutral 50 (OpenAI - 5.2)
Rating:50Neutral
Price Target:
$54.00
▲(0.80% Upside)
Action:ReiteratedDate:02/17/26
The score is held down mainly by weak financial performance (steep revenue contraction, large losses, and material cash burn), partially offset by low leverage and liquidity. Earnings-call commentary supports a mid-range outlook due to cost discipline and 2026 growth guidance, but FDA/regulatory uncertainty and H2 revenue concentration remain meaningful risks. Technically, longer-term trend support is constructive, though near-term price softness persists; valuation remains constrained by negative earnings and no dividend.
Positive Factors
Diversified late‑stage pipeline
Moderna's mRNA platform now supports multiple fully enrolled late‑stage oncology and registrational infectious disease programs, reducing single-product dependency. A broad, advanced pipeline increases the likelihood of nearer‑term, durable revenue streams beyond COVID if readouts are positive and approvals follow.
Proven commercial execution (MNEXT Spike)
A strong MNEXT Spike launch demonstrates Moderna's commercial and go‑to‑market capabilities, especially in high‑value older adult segments. Sustained market share in retail channels supports repeatable vaccine revenue and credibility for future product rollouts and international tender/market penetration.
Low leverage and improved cost structure
Moderna's modest debt load and multi‑billion cash position, combined with sustained cost cuts (operating expenses down ~30%), provide financial flexibility to fund R&D and commercial expansion. This stronger structural cost base lengthens runway and supports execution toward guided 2026 growth.
Negative Factors
Severe revenue contraction and cash burn
Revenue has fallen sharply from pandemic peaks, and operating/free cash flow turned deeply negative 2023–2025. Persistent cash burn erodes equity and requires either sustained revenue recovery, further cost cuts, or financing. This structural funding risk limits optionality for investing across programs.
Regulatory setback for flu program
An FDA refusal‑to‑file creates durable U.S. market access uncertainty for the flu franchise, removes an expected revenue pillar, and forces additional clinical/regulatory work. Management assumes no U.S. flu revenue in 2026, reducing upside and increasing reliance on non‑U.S. approvals and existing products.
Revenue seasonality and event‑driven reliance
Heavy H2 concentration and dependence on event‑driven readouts and international approvals make near‑term revenue volatile. This structural timing risk complicates cash flow planning, increases visibility risk for investors, and amplifies downside if key approvals or tender outcomes are delayed or unfavorable.

Moderna (MRNA) vs. SPDR S&P 500 ETF (SPY)

Moderna Business Overview & Revenue Model

Company DescriptionModerna, Inc., a biotechnology company, discovers, develops, and commercializes messenger RNA therapeutics and vaccines for the treatment of infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases, and auto-immune diseases in the United States, Europe, and internationally. Its respiratory vaccines include COVID-19, flu, respiratory syncytial virus, Endemic HCoV, and hMPV+PIV3 vaccines; latent vaccines comprise cytomegalovirus, epstein-barr virus, human immunodeficiency virus, herpes simplex virus, and varicella-zoster virus vaccines; and public health vaccines consists of Zika and Nipah vaccines. The company also offers systemic secreted and cell surface therapeutics; cancer vaccines, such as personalized cancer, KRAS, and checkpoint vaccines; intratumoral immuno-oncology products; localized regenerative, systemic intracellular, and inhaled pulmonary therapeutics. It has strategic alliances with AstraZeneca PLC; Merck & Co., Inc.; Vertex Pharmaceuticals Incorporated; Vertex Pharmaceuticals (Europe) Limited; Carisma Therapeutics, Inc.; Metagenomi, Inc.; the Defense Advanced Research Projects Agency; Biomedical Advanced Research and Development Authority; Institute for Life Changing Medicines; and The Bill & Melinda Gates Foundation, as well as a collaboration and license agreement with Chiesi Farmaceutici S.P.A. The company was formerly known as Moderna Therapeutics, Inc. and changed its name to Moderna, Inc. in August 2018. Moderna, Inc. was founded in 2010 and is headquartered in Cambridge, Massachusetts.
How the Company Makes MoneyModerna generates revenue primarily through the sale of its mRNA vaccines, most notably its COVID-19 vaccine, Spikevax, which has seen significant global demand since its emergency use authorization. The company's revenue model is largely driven by contracts with governments and health organizations for vaccine supply, resulting in substantial upfront payments and milestone payments. Additionally, Moderna engages in collaborations and partnerships with pharmaceutical companies and research institutions to develop its mRNA platform for other therapeutic areas, providing additional revenue through collaborative agreements and royalties. As the company expands its pipeline of mRNA-based therapies, potential future revenue streams may include sales from these new products and licensing agreements. Overall, the combination of vaccine sales, partnerships, and a growing pipeline of therapeutics contributes to Moderna's earnings.

Moderna Key Performance Indicators (KPIs)

Any
Any
Revenue by Segment
Revenue by Segment
Breaks down revenue across different business areas, revealing which segments are driving growth and how diversified Moderna's income streams are, indicating stability and strategic focus.
Chart InsightsModerna's revenue from product sales has faced significant volatility, with a sharp decline in recent quarters, reflecting the seasonal nature of its respiratory vaccine business. The latest earnings call highlights strategic pivots, including FDA approvals for new vaccines and substantial cost reductions, which are crucial as the company navigates a challenging revenue environment. Despite a strong cash position, shipment delays and workforce restructuring underscore the hurdles ahead. Moderna's focus on advancing its pipeline and achieving financial discipline aims to stabilize future performance amid these challenges.
Data provided by:The Fly

Moderna Earnings Call Summary

Earnings Call Date:Feb 13, 2026
(Q4-2025)
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% Change Since: |
Next Earnings Date:Apr 30, 2026
Earnings Call Sentiment Positive
The call highlights meaningful operational and commercial progress — notably strong MNEXT Spike launch, substantial cost reductions (operating expenses down 30%, cost of sales down 41%, R&D down 31%), improved losses and a healthy cash balance — alongside multiple clinical and commercial catalysts (fully enrolled late‑stage trials, strategic partnerships, international filings). Major risks include the FDA refusal to file for the flu vaccine, continued net losses and cash runoff toward 2026, and reliance on event‑driven readouts and international approvals for growth. Overall, the company demonstrated strong execution and cost discipline but faces material regulatory and timing risks that temper near‑term visibility.
Q4-2025 Updates
Positive Updates
Revenue and Quarterly Performance
Total 2025 revenue of $1.9B; Q4 revenue $700M (U.S. $300M; international $400M). Full-year U.S. revenue $1.2B (≈62% of total) and international $700M (≈38%). Q4 came in at the higher end of guidance.
Commercial Launch Success — MNEXT Spike
MNEXT Spike approved and launched in the U.S. in 2025 with a strong debut: 24% share of the total U.S. retail COVID market and 34% share among adults 65+. Also approved in Canada and Australia, with further international approvals targeted.
Significant Cost Reductions and Efficiency Gains
Operating expenses down $2.2B or 30% for the year; Q4 operating expenses down 31% YoY. Cost of sales decreased 41% YoY to $868M; R&D down 31% to $3.1B; SG&A down 13% to $1.0B. Company exceeded its 2025 cost reduction plan by over $1B vs. original guidance.
Improved Loss Metrics and Strong Cash Position
Full-year net loss improved to $2.8B from $3.6B in 2024; loss per share improved to $7.26 from $9.28 (≈22% improvement). Ended 2025 with $8.1B in cash and investments (includes $600M credit draw); excluding the draw would have been $7.6B—above prior guidance ranges.
Clear 2026 Financial Framework and Return-to-Growth Guidance
Guidance of up to 10% revenue growth in 2026 (driven primarily by international markets), projected cash costs of $4.2B, GAAP operating expenses ~$4.9B, and year-end 2026 cash guidance of $5.5–6.0B. Revenue expected to be weighted ~15% H1 / ~85% H2.
Pipeline Progress and Clinical Milestones
Positive five-year phase 2 data for INT (individualized cancer therapy) in adjuvant melanoma showing ~50% reduction in relapse/death. Multiple late-stage oncology studies fully enrolled (adjuvant melanoma, adjuvant RCC, muscle invasive bladder). Norovirus phase 3 and PA registrational study fully enrolled — potential readouts in 2026.
Strategic Partnerships and Geographic Expansion
New five-year strategic supply agreement with Mexico; commercialization agreement with Recordati for propionic acidemia (PA) rare disease program; full-year contributions expected from local manufacturing agreements in the U.K., Canada, and Australia in 2026.
Negative Updates
FDA Refusal to File (RTF) on Flu Vaccine (mRNA-1010)
FDA issued a refusal to file letter for the seasonal flu program (mRNA-1010). Management described this as a major disappointment and regulatory uncertainty; a Type A meeting has been requested but timing and requirements to refile remain unclear, creating U.S. market risk for the flu program.
Revenue Dependency and Conservative Assumptions
2026 guidance assumes no revenue from the flu vaccine or the flu‑COVID combination in the U.S., highlighting near-term reliance on COVID products, strategic partnerships, and MNEXT Spike. Full-year revenue remains heavily seasonal and concentrated (≈85% in H2), increasing timing risk.
Continued Net Loss and Cash Decline Outlook
Although improved, net loss remains $2.8B for 2025. Cash and investments declined from $9.5B at end-2024 to $8.1B at end-2025 and are forecast to decrease further to $5.5–6.0B by end-2026 (guidance does not assume additional credit draws).
Cost of Sales Decline Partly Reflects Lower Volumes and Write-Downs
Cost of sales fell 41% YoY, driven by productivity improvements but also by lower inventory write-downs, contract manufacturing wind-downs, and lower sales volumes — indicating business mix and demand headwinds for some products.
Regulatory Uncertainty Could Delay U.S. Access and Growth
Management flagged broader U.S. FDA regulatory unpredictability that could slow development timelines, delay patient access, and shift product availability to markets outside the U.S. before the U.S., increasing commercial uncertainty.
Dependence on Event-Driven Clinical Readouts
Key oncology and norovirus milestones are event- or case-driven (e.g., INT phase 3 melanoma and norovirus), so timing and outcomes are inherently uncertain. Several important readouts are expected in 2026 but remain contingent on event accrual.
Revenue Mix Shift and Market Dynamics
2025 revenue mix was U.S.-heavy (~62% U.S.), but 2026 expects a more balanced mix driven by international launches. Success depends on approvals and tender/market dynamics in diverse international markets where pricing and uptake vary.
Company Guidance
Moderna’s 2026 financial framework targets up to 10% revenue growth (with ~15% of revenue in H1 and ~85% in H2), a more balanced U.S./international mix vs ~62%/38% in 2025, and the start of locally manufactured sales in the U.K. and Australia; it projects cost of sales ≈ $900M (flat vs 2025’s $868M with gross‑margin improvement), R&D ≈ $3.0B (vs $3.1B in 2025), SG&A ≈ $1.0B (flat), total GAAP operating expenses ≈ $4.9B and cash costs ≈ $4.2B (ex‑stock comp, D&A), negligible taxes, capex $200–300M (including Norwood fill‑finish), and year‑end cash & investments of $5.5–6.0B (no further credit draws assumed). For context, 2025 results were: revenue $1.9B (Q4 $700M; Q4 U.S. $300M / international $400M; full‑year U.S. $1.2B / international $700M), cost of sales $868M (‑41% vs 2024), operating expenses down $2.2B (‑30%), net loss $2.8B (EPS ‑$7.26; Q4 net loss $800M / EPS ‑$2.11), year‑end cash & investments $8.1B (or $7.6B excluding a $600M initial credit draw), cash costs ~ $4.3B in 2025, and the company said it exceeded its 2025 cost‑reduction plan by over $1.0B.

Moderna Financial Statement Overview

Summary
Sharp post‑pandemic revenue contraction and continued large losses in 2023–2025, with operating and free cash flow deeply negative in 2023–2025. Offsetting positives include a comparatively strong, low‑leverage balance sheet that provides flexibility, but equity erosion and ongoing cash burn remain key risks.
Income Statement
28
Negative
Revenue has contracted sharply from the pandemic peak (2025 revenue of ~$1.9B vs. ~$18.9B in 2022), with continued declines in 2023–2025. While gross margin remains solid in 2024–2025 (~54–55%), the company is deeply unprofitable: 2023–2025 show large operating and net losses (2025 net margin roughly -145%), reflecting a cost structure that is not yet aligned to the lower revenue base. The main positive is that profitability was very strong in 2021–2022, indicating the model can produce high margins under the right demand conditions—but current earnings power is weak and the trajectory is still negative.
Balance Sheet
72
Positive
The balance sheet looks comparatively strong for a biotech: leverage is modest (debt is well below equity across the period; 2024 debt-to-equity ~0.07), providing financial flexibility. However, equity has trended down materially since 2022 (from ~$19.1B to ~$8.7B in 2025), consistent with sustained losses and cash burn, and returns on equity have been negative in 2023–2024. Overall, low debt is a clear strength, but continued losses are steadily eroding the capital base.
Cash Flow
24
Negative
Cash generation has deteriorated significantly: operating cash flow and free cash flow turned meaningfully negative in 2023–2025 (2025 operating cash flow about -$1.9B; free cash flow about -$2.1B), following strong positive cash flows in 2021–2022. Free cash flow also worsened versus the prior year in 2025, signaling ongoing cash burn. A partial offset is that free cash flow has generally moved in line with reported losses (free cash flow to net income above 1 in 2023–2025), but the magnitude of negative cash flow remains a key risk if revenue does not stabilize.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue1.94B3.20B6.85B18.88B17.74B
Gross Profit1.08B1.74B2.15B13.46B15.12B
EBITDA-2.55B-3.39B-3.28B9.77B13.53B
Net Income-2.82B-3.56B-4.71B8.36B12.20B
Balance Sheet
Total Assets12.34B14.14B18.43B25.86B24.67B
Cash, Cash Equivalents and Short-Term Investments5.80B7.03B8.60B9.90B10.73B
Total Debt1.92B747.00M1.24B1.20B916.00M
Total Liabilities3.69B3.24B4.57B6.74B10.52B
Stockholders Equity8.65B10.90B13.85B19.12B14.14B
Cash Flow
Free Cash Flow-2.06B-4.05B-3.83B4.58B13.34B
Operating Cash Flow-1.87B-3.00B-3.12B4.98B13.62B
Investing Cash Flow1.95B1.95B4.21B-5.18B-8.52B
Financing Cash Flow593.00M56.00M-1.38B-3.45B-873.00M

Moderna Technical Analysis

Technical Analysis Sentiment
Positive
Last Price53.57
Price Trends
50DMA
40.64
Positive
100DMA
33.39
Positive
200DMA
30.42
Positive
Market Momentum
MACD
3.21
Negative
RSI
74.64
Negative
STOCH
86.94
Negative
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For MRNA, the sentiment is Positive. The current price of 53.57 is above the 20-day moving average (MA) of 45.39, above the 50-day MA of 40.64, and above the 200-day MA of 30.42, indicating a bullish trend. The MACD of 3.21 indicates Negative momentum. The RSI at 74.64 is Negative, neither overbought nor oversold. The STOCH value of 86.94 is Negative, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for MRNA.

Moderna Risk Analysis

Moderna disclosed 73 risk factors in its most recent earnings report. Moderna reported the most risks in the "Tech & Innovation" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Moderna Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
62
Neutral
$5.88B-45.08-20.18%-35.39%-72.97%
59
Neutral
$20.22B-17.24-58.07%-100.00%-44.24%
53
Neutral
$13.41B-32.90-70.73%20.39%34.00%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
50
Neutral
$21.16B-7.38-28.87%-56.00%-38.95%
50
Neutral
$6.33B-29.83-244.45%54.92%28.47%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
MRNA
Moderna
53.57
23.30
76.97%
IONS
Ionis Pharmaceuticals
81.15
48.55
148.93%
PTGX
Protagonist Therapeutics
92.08
53.58
139.17%
RYTM
Rhythm Pharmaceuticals
92.73
40.33
76.97%
RVMD
Revolution Medicines
102.02
63.68
166.09%

Moderna Corporate Events

Business Operations and StrategyLegal ProceedingsProduct-Related AnnouncementsRegulatory Filings and Compliance
Moderna Faces FDA Setback on mRNA Flu Vaccine
Negative
Feb 11, 2026

On February 10, 2026, Moderna disclosed that the U.S. Food and Drug Administration’s Center for Biologics Evaluation and Research issued a Refusal-to-File letter on February 3, 2026 for its biologics license application for the investigational seasonal influenza vaccine mRNA-1010, declining to initiate review because the Phase 3 trial used a licensed standard-dose influenza vaccine comparator that regulators now say does not reflect the best-available standard of care. The decision, which did not raise safety or efficacy concerns and diverged from earlier FDA feedback on trial design, leaves Moderna seeking a Type A meeting to clarify a path forward even as mRNA-1010 remains under review in the EU, Canada and Australia based on two Phase 3 studies showing statistical superiority over comparators, and the company maintains that the U.S. setback will not affect its 2026 financial guidance.

The most recent analyst rating on (MRNA) stock is a Sell with a $27.00 price target. To see the full list of analyst forecasts on Moderna stock, see the MRNA Stock Forecast page.

Business Operations and StrategyFinancial DisclosuresPrivate Placements and Financing
Moderna updates 2025 outlook and highlights pipeline progress
Positive
Jan 12, 2026

On January 12, 2026, Moderna reported that it expected unaudited 2025 revenue of about $1.9 billion—slightly above prior guidance—alongside improved projected 2025 GAAP operating expenses of $5.0–$5.2 billion and an estimated year-end 2025 cash balance of $8.1 billion, supported in part by a $1.5 billion term loan facility. The company reiterated a framework of up to 10% revenue growth in 2026, further operating expense reductions through 2027 on a path to cash breakeven in 2028, and highlighted progress in its late-stage pipeline, including its approved mNEXSPIKE COVID vaccine, regulatory submissions and studies for RSV, flu, flu/COVID combination and norovirus vaccines, as well as advancing oncology candidates such as mRNA-4157 and mRNA-4359 and rare disease programs mRNA-3927 and mRNA-3705, underpinned by new funding support from Ares Management and CEPI for its H5 pandemic influenza candidate.

The most recent analyst rating on (MRNA) stock is a Hold with a $34.00 price target. To see the full list of analyst forecasts on Moderna stock, see the MRNA Stock Forecast page.

Business Operations and StrategyFinancial DisclosuresPrivate Placements and FinancingProduct-Related Announcements
Moderna Highlights 2025 Progress and Strengthened Vaccine Portfolio
Positive
Jan 5, 2026

In a January 5, 2026 letter to shareholders, Moderna reviewed a challenging 2025 operating environment in the U.S. but highlighted strong execution that yielded three approved commercial products, multiple new regulatory approvals and a more stable seasonal vaccine business. The company reported that mNEXSPIKE’s U.S. launch in 2025 rapidly made it the leading product in the retail COVID-19 channel, accounting for roughly a quarter of all U.S. retail COVID vaccinations and nearly a third among adults 65 and older, while long-term public-sector and international partnerships in the UK, Canada, Australia, Brazil and Taiwan strengthened revenue visibility and global access to its mRNA vaccines. Moderna advanced its pipeline with U.S. approvals and label expansions for its COVID-19 and RSV vaccines, positive Phase 3 data and global submissions for its flu and flu/COVID combination candidates, continued progress of its personalized cancer therapy intismeran autogene and other oncology programs, and key milestones in rare disease candidates mRNA-3927 and mRNA-3705. At the same time, the company tightened financial discipline, cutting GAAP operating expenses from $11.1 billion in 2023 to an expected level below $5.5 billion in 2025, securing a $1.5 billion term loan facility, and targeting cash breakeven in 2028, while increasingly using AI tools to improve R&D, forecasting and operations as it enters 2026 positioned for its next phase of growth.

The most recent analyst rating on (MRNA) stock is a Hold with a $35.00 price target. To see the full list of analyst forecasts on Moderna stock, see the MRNA Stock Forecast page.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Feb 17, 2026