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Ascendis Pharma (ASND)
NASDAQ:ASND
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Ascendis Pharma (ASND) AI Stock Analysis

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ASND

Ascendis Pharma

(NASDAQ:ASND)

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Neutral 57 (OpenAI - 5.2)
Rating:57Neutral
Price Target:
$248.00
▲(8.29% Upside)
Action:ReiteratedDate:02/14/26
The score is driven primarily by improving fundamentals (rapid revenue growth, strong margins, and a move to positive operating/free cash flow) but is held back by balance-sheet risk (negative equity and high debt) and unprofitable earnings (negative P/E). Technicals are neutral-to-slightly cautious, while the latest earnings call adds support via upbeat guidance and commercial/pipeline momentum despite elevated operating expenses and near-term volatility risks.
Positive Factors
Commercial momentum
Rapid, recurring product sales from Yorvipath and Skytrofa create a durable commercial revenue base. Broad geographic availability and thousands of U.S. patients support scale in access, payer relationships and field capabilities, reducing reliance on one-off events for cash generation.
High gross margins and revenue scaling
Very high gross margins combined with rapid revenue scaling signal strong product economics and favorable unit contribution. This structural margin advantage permits operating leverage as sales grow, improving the odds of sustainable profitability if SG&A and R&D growth are managed.
Improving cash generation
A move to positive operating and free cash flow, alongside a sizable cash balance, materially strengthens near‑term funding flexibility. Durable cash generation reduces dependence on external capital for launches and supports continued pipeline investment and selective capital returns.
Negative Factors
Leverage & negative equity
Negative equity and substantial debt materially constrain financial flexibility. Elevated leverage raises refinancing and covenant risk, could force dilutive financing or constrain R&D/launch spend if growth or cash flow falters, and increases sensitivity to macro or interest‑rate shocks.
High operating expense run-rate
Operating expenses exceeding sales indicate a high fixed cost base that can erode margins if revenue growth slows. Sustained elevated OpEx requires tight discipline to deliver durable profit expansion and risks reversing recent cash generation gains if launch or access costs rise.
Early U.S. penetration and access friction
Low initial penetration and non‑universal payer approvals are structural adoption hurdles. Scaling to meaningful market share will require ongoing prescriber uptake, improved reimbursement rates and patient support; slow progress here can delay peak sales and extend promotional spend.

Ascendis Pharma (ASND) vs. SPDR S&P 500 ETF (SPY)

Ascendis Pharma Business Overview & Revenue Model

Company DescriptionAscendis Pharma A/S, a biopharmaceutical company, focuses on developing therapeutics for unmet medical needs. The company offers SKYTROFA for treating patients with growth hormone deficiency (GHD). It also develops TransCon Growth Hormone (hGH) for pediatric GHD in Japan; TransCon hGH for adults with GHD; TransCon parathyroid hormone for adult hypoparathyroidism; and TransCon CNP for pediatric achondroplasia. In addition, the company develops TransCon toll like receptors 7/8 agonist for intratumoral delivery; and TransCon IL-2 ß/g for systemic delivery. The company was incorporated in 2006 and is headquartered in Hellerup, Denmark.
How the Company Makes MoneyAscendis Pharma generates revenue primarily through the commercialization of its biopharmaceutical products, which include approved therapies and those in various stages of clinical trials. The company earns income from product sales, licensing agreements, and partnerships with other pharmaceutical companies for research and development collaborations. Significant revenue streams include sales from its flagship products as well as milestone payments and royalties from licensing agreements. Partnerships with larger pharmaceutical firms also contribute to its earnings by providing funding for clinical development and potential future sales of co-developed products.

Ascendis Pharma Key Performance Indicators (KPIs)

Any
Any
Commercial Products Revenue
Commercial Products Revenue
Shows the income generated from products that have reached the market, indicating the company's ability to convert R&D efforts into profitable offerings and its success in capturing market share.
Chart InsightsAscendis Pharma's Yorvipath saw a remarkable revenue surge starting in late 2024, reflecting a successful market launch. This aligns with the company's earnings call, highlighting strong demand and significant patient uptake in the US and global markets. Despite challenges like insurance approval rates and currency impacts, Yorvipath's growth is bolstered by strategic geographic expansion and robust healthcare provider engagement. The company's positive operating profit and cash flow management further underscore its financial transformation, with expectations for continued revenue growth driven by new patient enrollments and market entries.
Data provided by:The Fly

Ascendis Pharma Earnings Call Summary

Earnings Call Date:Feb 11, 2026
(Q4-2025)
|
% Change Since: |
Next Earnings Date:May 27, 2026
Earnings Call Sentiment Positive
Overall the call was constructive and growth-focused: management reported strong commercial execution (notably Yorvipath and Skytrofa), meaningful pipeline and regulatory progress (including imminent PDUFA for TransCon CNP and compelling combination data), and a strengthened cash position with an ambitious operating cash flow outlook for 2026. Key headwinds include high operating expenses (which slightly exceeded 2025 revenue), a substantial noncash finance remeasurement loss, currency-driven revenue headwinds, and remaining access / penetration and competitive uncertainties. Taken together the positives around revenue momentum, pipeline advancement, partnerships, and a stronger financial base outweigh the near-term financial and market-access challenges.
Q4-2025 Updates
Positive Updates
Yorvipath revenue surge and broadening access
Q4 2025 Yorvipath revenue of €187,000,000, up from €140,000,000 in Q3 2025 (+33.6% quarter-over-quarter); full-year 2025 revenue €477,000,000. More than 5,300 US patients prescribed by ~2,400 prescribers; insurance approval rate ~70% with majority approved within eight weeks. Yorvipath available commercially or via named-patient programs in >30 countries, with full commercial reimbursement in multiple markets and 10 additional full commercial launches expected in 2026.
Skytrofa solid commercial performance
Skytrofa Q4 2025 revenue €53,000,000 and full-year 2025 revenue €206,000,000; achieved ~7% overall US market share. Launched Phase III basket trial to expand indications (ISS, SHOX deficiency, Turner syndrome, SGA) representing up to ~50% of the growth hormone market.
Company revenue, cash and operating cash flow
Total Q4 2025 revenue €248,000,000 (including €7,000,000 collaboration revenue); total 2025 revenue €720,000,000. Year-end cash and cash equivalents €616,000,000, up from €560,000,000 (+~10%). Q4 operating cash flow €73,000,000.
Pipeline and regulatory momentum
TransCon CNP NDA under FDA review with a PDUFA date of Feb 28, 2026; Phase II 52-week combination data showed 3–4x linear growth improvement versus monotherapy and meaningful benefits in body proportionality and arm span without compromising safety. End-of-Phase-2 and scientific advice meetings with FDA/EU were positive and Phase III alignment achieved. Progress on once-weekly TransCon PTH preclinical PK/PD supporting a weekly profile comparable to daily therapy; Phase III/label-expansion programs moving forward. Strategic partnerships (e.g., Novo Nordisk for once-monthly semaglutide) are advancing toward the clinic.
Ambitious financial outlook
Management expects operating cash flow of ~€500,000,000 in 2026 and aspires to at least €5,000,000,000 in annual product revenue by 2030, reflecting strong confidence in the commercial rollout and pipeline value.
Negative Updates
Operating expenses exceed full-year revenue
Full-year 2025 operating expenses €761,000,000 versus revenue €720,000,000 — operating expenses exceeded revenue by ~€41,000,000 (≈5.7% of revenue). Q4 operating expenses were €214,000,000, indicating a high expense run rate that management expects to monitor in 2026.
Large noncash finance remeasurement loss
Noncash remeasurement loss of financial liabilities of €106,000,000 contributed to a net noncash finance expense of €93,000,000, materially impacting below-operating-profit results despite a relatively small net cash finance expense (~€8,000,000 for the year).
Currency headwinds reduced reported revenue
Weaker US dollar negatively impacted full-year reported revenue: ~€27,000,000 reduction for Yorvipath and ~€9,000,000 reduction for Skytrofa (combined ~€36,000,000 impact).
U.S. penetration and access still early
Despite strong launch metrics, management notes that <5% of the US patient population is currently on Yorvipath treatment, and the insurance approval rate (~70%) indicates remaining access work. Ex-US uptake is heterogeneous (different reimbursement and provider bottlenecks), and seasonality / quarter-to-quarter variability was highlighted as a modeling consideration.
Competitive and clinical uncertainties
Management acknowledged competitive entrants and alternative approaches (e.g., encaleret, FGFR inhibitors, long-acting CNPs) and expressed concerns about nonspecific FGFR inhibitors' potential safety risks. These competing programs and the evolving landscape create execution and safety/efficacy scrutiny risk for future uptake.
Near-term guidance exclusions and launch uncertainty
TransCon CNP was explicitly excluded from the 2026 outlook pending regulatory outcomes; management noted potential seasonality (Q1 impacts) and that launch-related investment and early revenue contribution will be clarified post-approval — introducing near-term forecasting uncertainty.
Company Guidance
Management guided to operating cash flow of around €500,000,000 in 2026 and reiterated an aspiration of at least €5,000,000,000 in annual product revenue by 2030; they expect continued strong Yorvipath revenue growth in 2026 (Q4 2025 Yorvipath €187,000,000; FY2025 €477,000,000), Skytrofa to follow a similar seasonal pattern (Q4 2025 €53,000,000; FY2025 €206,000,000; ~7% US market share), and noted TransCon CNP’s PDUFA on Feb 28 (excluded from the 2026 outlook). Quarterly company results included total Q4 revenue €248,000,000 (incl. €7,000,000 collaboration), FY2025 revenue €720,000,000, Q4 operating profit €10,000,000, Q4 operating cash flow €73,000,000, Q4 OpEx €214,000,000 and FY OpEx €761,000,000; cash was €616,000,000 at year‑end (up from €560,000,000), FX reduced Yorvipath by ~€27,000,000 and Skytrofa by ~€9,000,000, and noncash remeasurement loss was €106,000,000 (net noncash finance expense €93,000,000; net cash finance expense ~€8,000,000). Commercial metrics: >5,300 US patients prescribed Yorvipath by ~2,400 prescribers, <5% US patient penetration, ~70% insurance approval rate with most approvals within eight weeks, availability in >30 countries, full reimbursement in 4 European and 2 international markets, Japan launch Nov 2025, and 10 additional full commercial launches expected in 2026.

Ascendis Pharma Financial Statement Overview

Summary
Strong revenue acceleration and very high gross margins, plus a 2025 inflection to positive operating and free cash flow. Offsetting this, the company remains net-loss making and the balance sheet is a key risk with negative equity and substantial debt, limiting financial flexibility.
Income Statement
34
Negative
Revenue is scaling quickly, rising from $266.7M (2023) to $363.6M (2024) to $691.7M (2025), and gross margin remains very strong (~85% in 2025), consistent with an attractive product mix. However, the company is still meaningfully loss-making, with negative operating profit and EBITDA in every year shown; while profitability is improving materially (net margin improved from about -104% in 2024 to about -32% in 2025), earnings are not yet positive and execution risk remains if expense growth re-accelerates.
Balance Sheet
22
Negative
Leverage risk is elevated because shareholders’ equity is negative in 2023–2025 (e.g., -$162.8M in 2025) while total debt is high (~$871.4M in 2025). Total assets increased (to ~$1.30B in 2025), but the negative equity position reduces financial flexibility and can pressure future funding options, particularly important for a biotechnology business that may need continued investment.
Cash Flow
46
Neutral
Cash generation improved sharply in 2025, with operating cash flow turning positive (~$51.8M) and free cash flow also positive (~$43.6M), a notable step up from large cash burn in 2023–2024. The key weakness is volatility: free cash flow growth swung sharply negative in 2025 versus 2024, and overall cash flow history shows multiple years of sizable outflows, so durability of the recent positive turn still needs to be proven.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue691.71M363.64M266.72M51.17M7.78M
Gross Profit588.53M319.38M222.32M39.04M4.25M
EBITDA-113.90M-290.02M-411.17M-529.18M-364.64M
Net Income-219.03M-378.08M-481.45M-583.19M-383.58M
Balance Sheet
Total Assets1.30B1.18B825.59M1.09B1.08B
Cash, Cash Equivalents and Short-Term Investments615.78M559.54M399.44M735.46M682.06M
Total Debt871.41M856.62M743.06M617.57M209.92M
Total Liabilities1.46B1.29B971.28M826.39M201.29M
Stockholders Equity-162.75M-105.71M-145.70M263.35M883.63M
Cash Flow
Free Cash Flow43.62M-307.62M-469.80M-510.19M-441.88M
Operating Cash Flow51.77M-306.20M-467.36M-495.70M-417.65M
Investing Cash Flow-8.15M6.88M286.47M61.73M-110.58M
Financing Cash Flow34.89M443.93M134.29M396.77M351.39M

Ascendis Pharma Technical Analysis

Technical Analysis Sentiment
Positive
Last Price229.01
Price Trends
50DMA
223.99
Positive
100DMA
215.00
Positive
200DMA
200.26
Positive
Market Momentum
MACD
3.35
Positive
RSI
48.59
Neutral
STOCH
33.18
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For ASND, the sentiment is Positive. The current price of 229.01 is below the 20-day moving average (MA) of 231.90, above the 50-day MA of 223.99, and above the 200-day MA of 200.26, indicating a neutral trend. The MACD of 3.35 indicates Positive momentum. The RSI at 48.59 is Neutral, neither overbought nor oversold. The STOCH value of 33.18 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for ASND.

Ascendis Pharma Risk Analysis

Ascendis Pharma disclosed 93 risk factors in its most recent earnings report. Ascendis Pharma reported the most risks in the "Finance & Corporate" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Ascendis Pharma Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
85
Outperform
$23.87B16.1719.30%13.50%17.16%
76
Outperform
$10.69B12.1036.88%9.93%54.33%
74
Outperform
$11.36B32.675.82%12.31%60.21%
57
Neutral
$14.06B-50.22127.54%103.32%47.55%
55
Neutral
$10.06B-45.32-43.76%864.21%48.12%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
50
Neutral
$13.18B-20.6939.18%62.46%-73.59%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
ASND
Ascendis Pharma
229.01
76.70
50.36%
BMRN
BioMarin Pharmaceutical
59.07
-11.53
-16.33%
EXEL
Exelixis
41.17
4.37
11.88%
MDGL
Madrigal Pharmaceuticals
438.73
115.71
35.82%
UTHR
United Therapeutics
532.82
227.43
74.47%
BBIO
BridgeBio Pharma
67.98
35.67
110.40%

Ascendis Pharma Corporate Events

Ascendis Pharma Wins FDA Accelerated Approval for YUVIWEL in Pediatric Achondroplasia
Mar 2, 2026

On February 27, 2026, Ascendis Pharma announced that the U.S. Food & Drug Administration granted accelerated approval for YUVIWEL (navepegritide; developed as TransCon CNP), the first and only once-weekly treatment to increase linear growth in children aged two and older with achondroplasia with open epiphyses. The drug, a prodrug of C-type natriuretic peptide designed for continuous systemic exposure, addresses overactive FGFR3 signaling in this rare skeletal dysplasia, which is associated with muscular, neurological and cardiorespiratory complications.

The approval, supported by safety and efficacy data from three randomized, double-blind, placebo-controlled trials plus up to three years of extension data, was based on improvement in annualized growth velocity and remains contingent on confirmation of clinical benefit in follow-up studies. Ascendis expects to launch YUVIWEL in the U.S. in early second quarter 2026 with dedicated patient support through its Ascendis Signature Access Program and received a Rare Pediatric Disease Priority Review Voucher, enhancing its strategic position in rare pediatric disorders and potentially accelerating future product reviews.

The most recent analyst rating on (ASND) stock is a Buy with a $256.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Sets March 23 AGM to Approve 2025 Results, Board Changes and Buyback Mandate
Feb 23, 2026

Ascendis Pharma has called its 2026 annual general meeting for March 23, 2026 in Copenhagen, where shareholders will review the company’s activities in 2025, approve the audited annual report and sustainability and P-ESG report for the year ended December 31, 2025, and vote on discharging the board and management from liability. The board will also seek approval to carry forward a consolidated loss of EUR 228 million into accumulated deficit, re-elect the current directors and add industry veteran Jean-Jacques Bienaimé as a new non-executive member, appoint Deloitte as auditor, and extend authority for share buybacks, decisions that shape governance, capital structure flexibility, and oversight for investors ahead of the next phase of the company’s development.

The most recent analyst rating on (ASND) stock is a Buy with a $256.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Posts Strong 2025 Results as YORVIPATH Drives Growth and TransCon Pipeline Advances
Feb 11, 2026

Ascendis Pharma reported on February 11, 2026 that fourth-quarter 2025 product revenue reached €240 million and full-year 2025 product revenue €684 million, driven mainly by YORVIPATH, while SKYTROFA contributed €206 million for the year. The company posted a Q4 2025 operating profit of €10 million, generated €73 million in operating cash flow, ended 2025 with €616 million in cash, and plans to start a €120 million share repurchase program in 2026.

Operationally, Ascendis highlighted rapid global uptake of YORVIPATH with more than 5,300 U.S. patient enrollments and availability in over 30 countries, plus commercial launches expected in 10 more markets by year-end 2026. The pipeline advanced with TransCon CNP under FDA priority review with a February 28, 2026 action date, an EMA filing, positive Phase 2 COACH data for TransCon CNP plus TransCon hGH, new Phase 3 and basket trials, and progress in oncology and partnered programs such as a Novo Nordisk obesity collaboration and VISEN’s Chinese approval of TransCon hGH.

These developments position Ascendis for a potential “steep growth phase” as management targets approximately €500 million in operating cash flow in 2026 and aspires to at least €5 billion in annual product revenue by 2030. Growing recurring product sales, broader geographic reach through partners like Teijin and VISEN, and a diversified late-stage pipeline strengthen its standing in the global biopharma market and may enhance value for shareholders and patients in endocrine, metabolic, and oncology indications.

The most recent analyst rating on (ASND) stock is a Buy with a $250.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Grants New Employee Warrants, Updates Articles to Support Future Equity Issuances
Feb 11, 2026

On February 10, 2026, Ascendis Pharma’s board granted 16,570 new employee warrants, each giving the right to subscribe for one ordinary share at an exercise price of $224.19, matching the closing price of its American depositary shares on the grant date. The warrants, issued under an appendix to the company’s Articles of Association, vest over four years with 25% vesting after one year and the remainder monthly thereafter, and leave 1,666,633 additional warrants available for future grants, underscoring the company’s continued reliance on equity-based incentives to retain and motivate staff.

In connection with these grants, Ascendis amended its Articles of Association, which also set out broader capital-raising tools including additional warrant programs, share capital increases and convertible bond authorizations. These mechanisms collectively provide the company with flexibility to fund growth, align employee and shareholder interests, and manage its capital structure without necessarily resorting to traditional rights offerings for existing shareholders.

The most recent analyst rating on (ASND) stock is a Buy with a $250.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Grants New Employee Warrants, Updates Articles of Association
Jan 14, 2026

On January 13, 2026, Ascendis Pharma’s board of directors granted 42,030 warrants to certain employees, each warrant entitling the holder to subscribe for one ordinary share at an exercise price of $215.05, matching the closing price of the company’s American Depositary Shares on the grant date. The award, which vests over four years subject to continued service and potential accelerated vesting upon specific exit events, required an amendment to the company’s Articles of Association and leaves a further 1,683,203 warrants available for future issuance, signaling continued use of equity-based incentives and potential future dilution for shareholders as part of Ascendis Pharma’s long-term employee retention and alignment strategy.

The most recent analyst rating on (ASND) stock is a Buy with a $250.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Sets 2026 Milestones and Unveils $120 Million Share Buyback
Jan 12, 2026

On January 9, 2026, Ascendis Pharma outlined a 2026 business and strategic roadmap highlighting strong commercial uptake of YORVIPATH, which had more than 5,300 unique U.S. patient enrollments and broad international availability by year-end 2025, with further launches planned in at least 10 additional countries by the end of 2026 and continued label-expansion trials. The company noted that SKYTROFA secured its first U.S. label expansion in July 2025 for adult growth hormone deficiency and that a Phase 3 basket trial is underway for additional growth-related indications, while its TransCon CNP program is advancing toward key regulatory decisions in the U.S. and Europe for pediatric achondroplasia and into Phase 3 combination studies with TransCon hGH following positive Phase 2 COACH Trial data reported on January 8, 2026. Ascendis also flagged upcoming 2026 data readouts for its TransCon IL-2 β/γ oncology program, progress of partnered assets with Novo Nordisk in obesity and metabolic disease and with Eyconis in ophthalmology, and regulatory momentum in Greater China and Japan via VISEN Pharmaceuticals and Teijin Limited, including an expected early-2026 approval in China for pediatric growth hormone deficiency and an existing Japanese approval of YORVIPATH in August 2025. In a capital allocation move that may support shareholder value and signal confidence in its outlook, the board authorized a $120 million share repurchase program, giving the company flexibility to buy back stock in the open market or through other permitted methods depending on market conditions and other factors.

The most recent analyst rating on (ASND) stock is a Buy with a $246.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Posts Strong Year-Long Phase 2 COACH Data for TransCon CNP and hGH Combo in Achondroplasia
Jan 9, 2026

On January 8, 2026, Ascendis Pharma reported positive Week 52 topline data from its Phase 2 COACH trial, the first study to evaluate once-weekly combination therapy with TransCon CNP and TransCon hGH in children aged 2 to 11 years with achondroplasia, showing durable increases in growth velocity, improved body proportionality and arm span, and no new safety concerns compared with the individual monotherapies. The results, which included annualized growth velocities above the 97th percentile of average-stature children and maintenance of bone age in line with chronological age, support Ascendis’s strategy to advance a Phase 3 program in pediatric achondroplasia and could strengthen the company’s position in the rare endocrine and skeletal dysplasia market as TransCon CNP undergoes priority regulatory review in the U.S. and Europe and all enrolled children continue on treatment in the COACH trial.

The most recent analyst rating on (ASND) stock is a Buy with a $242.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Ups Share Capital After Warrant Exercises in December 2025
Dec 30, 2025

On December 30, 2025, Ascendis Pharma A/S reported that a scheduled exercise window for its outstanding warrants exercisable into ordinary shares had closed, resulting in a registered increase of its share capital by a nominal DKK 282,197. This brought the company’s total share capital to a nominal DKK 61,977,408 through the issuance of 282,197 new ordinary shares at an average cash consideration of about USD 63.34 per share, strengthening its equity base. In connection with these changes, Ascendis updated and registered amended articles of association with the Danish Business Authority, underscoring the company’s continued use of equity-based incentives and capital market instruments as part of its financing and corporate governance framework.

The most recent analyst rating on (ASND) stock is a Buy with a $250.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND Stock Forecast page.

Ascendis Pharma Grants Employee Warrants to Strengthen Market Position
Dec 10, 2025

On December 9, 2025, Ascendis Pharma’s board of directors granted 27,820 warrants to certain employees, allowing them to subscribe for ordinary shares at an exercise price of $196.63 per share. This move is part of the company’s strategy to incentivize employees and aligns with its Articles of Association, which were amended to accommodate this grant. The vesting schedule for these warrants includes a 25% vesting after one year and the remainder vesting monthly over the next three years, contingent on continued service. This grant leaves 1,725,233 shares available for future warrants, highlighting Ascendis Pharma’s ongoing commitment to leveraging employee incentives to bolster its market position.

The most recent analyst rating on (ASND) stock is a Buy with a $220.00 price target. To see the full list of analyst forecasts on Ascendis Pharma stock, see the ASND 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 14, 2026