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Krystal Biotech (KRYS)
NASDAQ:KRYS

Krystal Biotech (KRYS) AI Stock Analysis

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KRYS

Krystal Biotech

(NASDAQ:KRYS)

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Outperform 81 (OpenAI - 5.2)
Rating:81Outperform
Price Target:
$319.00
▲(17.06% Upside)
Action:ReiteratedDate:02/18/26
Score is driven primarily by strong financial performance (profitability and cash flow improvement with minimal leverage) and a constructive earnings outlook (high-margin guidance, strong cash runway, and positive pipeline/regulatory progress). Offsetting factors are premium valuation (P/E ~41.5) and some near-term execution/visibility risks (higher planned spend and European pricing/revenue timing), while technicals remain positive but not strongly overextended.
Positive Factors
Balance sheet health
Extremely low leverage and materially higher equity provide durable financial flexibility. This balance sheet supports multi-year commercial rollouts, funds pipeline milestones without near-term refinancing, and reduces solvency risk—important for a biotech scaling global launches and R&D spend.
Robust cash generation
High operating cash flow and near-complete free cash flow conversion mean earnings are largely cash-backed. That sustains self-funding for launches and registrational studies, lowers dilution risk, and provides a multi-quarter runway to execute strategy even with stepped-up investment.
Platform & clinical progress
Demonstrated gene delivery in pulmonary tissue validates the HSV-1 Skin TARGET platform's versatility beyond dermatology. Positive molecular and safety readouts plus planned repeat-dosing/registrational steps materially expand addressable markets and support a multi-product growth thesis over coming years.
Negative Factors
Rising operating expense guidance
Planned step-up in combined R&D and SG&A is structural as the company scales international launches and multiple registrational programs. If top-line growth or European reimbursement lags, higher fixed operating costs could compress margins and slow free cash flow expansion.
Higher non‑U.S. COGS & Europe pricing risk
Rising unit costs outside the U.S. and unresolved European pricing create durable margin and revenue-recognition uncertainty. International launch economics and reimbursement timing will materially affect profitability and predictability as the company pursues broader geographic rollouts.
Limited track record & data inconsistencies
Recent profitability is encouraging but short-lived relative to earlier loss years, and noted margin field anomalies in 2025 introduce modeling risk. Biotech outcomes and commercial execution can swing results; durability of margins and earnings requires monitoring across cycles.

Krystal Biotech (KRYS) vs. SPDR S&P 500 ETF (SPY)

Krystal Biotech Business Overview & Revenue Model

Company DescriptionKrystal Biotech, Inc., a clinical stage biotechnology company, engages in the field of redosable gene therapy to treat serious rare diseases in the United States. Its lead product candidate is beremagene geperpavec (B-VEC), which is in Phase III clinical study to treat dystrophic epidermolysis bullosa. The company is also involved in developing KB105 that is in Phase I/II clinical study for treating patients with deficient autosomal recessive congenital ichthyosis; KB301, which is in Phase I/II clinical stage for treating wrinkles and other presentations of aged or damaged skin; KB407 that is in preclinical stage for cystic fibrosis; and KB104, which is in preclinical stage for netherton syndrome. Its discovery stage product candidates include KB5xx for treating chronic skin diseases, KB3xx to treat aesthetic skin conditions, and KB3xx product. Krystal Biotech, Inc. was founded in 2015 and is headquartered in Pittsburgh, Pennsylvania.
How the Company Makes MoneyKrystal Biotech generates revenue primarily through the commercialization of its gene therapy products. This includes product sales from approved therapies, which can be substantial given the high demand for effective treatments in rare diseases. Additionally, the company may enter into strategic partnerships with pharmaceutical companies or research institutions to develop and market its products, which can provide upfront payments, milestone payments, and royalties based on future sales. The ongoing development of new therapies and potential expansions into additional markets also contribute to their revenue streams.

Krystal Biotech Earnings Call Summary

Earnings Call Date:Feb 17, 2026
(Q4-2025)
|
% Change Since: |
Next Earnings Date:May 11, 2026
Earnings Call Sentiment Positive
The call conveyed solid commercial momentum and strong financial results (notably $107.1M Q4 revenue, 34% Y/Y full-year growth, 94% gross margin, and ~$956M cash) together with important pipeline breakthroughs (KB407 CF transduction data) and regulatory designations (RMAT, Fast Track). Key risks include rising operating expenses, higher COGS for non-U.S. sales, ongoing pricing negotiations in Europe that create near-term revenue visibility risk, and operational/compliance frictions in early international launches. On balance, the positive commercial traction, strong margins and cash position, and multiple promising clinical developments outweigh the operational and timing headwinds described.
Q4-2025 Updates
Positive Updates
Strong Q4 and Full-Year Revenue
Q4 net revenue from VYJEVEC was $107.1M; year-to-date net revenue was $389.1M, representing ~34% growth versus full year 2024. Q4 revenue rose nearly 10% versus the prior quarter and ~18% versus prior-year Q4. Total net VYJEVEC revenue since launch exceeds $730M.
High Gross Margins and Profitability
Reported gross margin was 94% for the quarter and full year (guidance 90–95% expected going forward). Net income was $51.4M in Q4 ($1.77 basic / $1.70 diluted) and $204.8M for the full year ($7.08 basic / $6.84 diluted), aided by a one-time noncash tax benefit.
Strong Cash Position
Year-end combined cash and investments totaled $955.9M, providing substantial runway to support global launches and pipeline milestones.
Commercial Momentum and Global Launch Progress
US commercial momentum: added >50 new prescribers in Q4 and >500 unique prescribers since launch; reimbursement approval acceleration for three consecutive quarters with >60 approvals since launch. Distributor agreements now cover >20 countries with a goal to expand to >40 in 2026; expanded distributor network to include Israel.
Early International Adoption
Launches in Germany, France (AP2 early access), and Japan progressed with estimated >90 patients prescribed across Germany, France and Japan combined; Japan pricing negotiated and local distribution model enabling home delivery implemented.
Pipeline Breakthroughs — KB407 (CF)
KB407 showed successful delivery and expression of full-length wild-type CFTR in lung biopsies. Observed transduction rates ranged 29%–42% across biopsied patients (including modulator-ineligible), with apical CFTR expression and durability out to at least 96 hours. Repeat-dosing study planning with expectation to start repeat dosing in H1.
Registrational Program Updates and Home Dosing Enablement
Protocol updates: KB801 (EMERALD-1) up-sized to ~60 patients and dosing modified to allow once-daily home or caregiver administration; KB803 amended to allow three-times-weekly home administration. Over half of clinical sites activated and the company expects data readouts for these programs before year-end.
Regulatory Designations and Recognition
FDA granted Fast Track designation for KB111 and RMAT designation for KB707, supporting accelerated pathways. VYJEVEC received the Prix Galien in France for innovation and clinical impact.
Negative Updates
Compression in Gross Margin and Higher COGS Outside U.S.
Quarter gross margin dipped to 94% from 96% in Q3 and 95% in prior-year Q4. Cost of goods sold rose to $6.6M (Q3: $4.3M; prior-year Q4: $4.9M) driven by increased volume sold outside the U.S. and higher per-unit costs ahead of manufacturing process optimizations.
Rising Operating Costs and Higher 2026 Expense Guidance
SG&A rose to $41.4M in Q4 from $31.3M in prior-year Q4 (~+32%) driven by headcount, legal/consulting, and marketing for global launches. R&D was $14.8M (prior-year Q4 $13.5M). Company guides 2026 non-GAAP R&D + SG&A to $175–195M versus 2025 actual $150.3M (implying a notable increase in planned spend).
Revenue Recognition and Pricing Uncertainty in Europe
Pricing negotiations ongoing in Germany and France; company cautions revenue may not track linearly with patient counts in 2026 due to accruals, timing effects and unresolved pricing. Management expects pricing alignment in Germany in 2026 and France later (timeline uncertain), creating short-term visibility risk.
Compliance and Access Frictions — Japan Specifics
Japan requires two-week prescriptions in the first year, adding patient burden and potential compliance drop-offs; company notes this could depress compliance in early launch phases until later when processes normalize.
Limited Granularity on International Patient Metrics
The reported estimate of >90 patients prescribed across Germany, France and Japan is approximate and based on proxies (vials/pharmacies); management noted difficulty segmenting patient counts by country, limiting near-term visibility into true uptake by geography.
Home-Dosing Introduces Operational Risks
Shifts to home or caregiver administration (KB801 daily, KB803 three-times-weekly) were implemented to improve convenience, but introduce potential for user administration errors; dosing regimens were adjusted to mitigate this risk, which may affect comparability to prior data.
Capital Allocation — Share Buyback Unlikely Near-Term
Management indicated share buybacks are not likely near-term given pipeline and launch funding priorities and will not be using cash for in-licensing or acquisitions at present, which may disappoint return-focused investors.
Company Guidance
Management guided gross margins to remain in the 90%–95% range and gave 2026 non‑GAAP R&D+SG&A guidance of $175–195M (up from YTD 2025 non‑GAAP spend of $150.3M); they reported Q4 net product revenue of $107.1M (≈10% growth vs prior quarter, ≈18% vs Q4 2024), YTD revenue of $389.1M (≈34% vs 2024) and cumulative revenue since launch of >$730M, with Q4 COGS $6.6M, Q4 R&D $14.8M, Q4 SG&A $41.4M, stock‑based comp $13.8M, Q4 net income $51.4M ($1.77 basic / $1.70 diluted), FY net income $204.8M ($7.08 / $6.84) and $955.9M in cash & investments; commercial expansion targets include distributor agreements in >20 countries with a goal of >40 in 2026, >90 patients prescribed across Germany/France/Japan and an Italy launch in 2H‑2026 (pricing negotiations expected in Germany through 2026 and France into 2027, which may cause non‑linear revenue recognition), and clinical guidance includes KB407 repeat‑dosing beginning H1 (observed transduction 29%–42% and durability ≥96 hours), an upsized KB801 registrational study (~60 patients, ~30 sites with >50% activated) and KB803 (3×/week dosing) both targeting data readouts before year‑end, plus KB408 updates and regulatory designations (KB707 RMAT; KB111 Fast Track).

Krystal Biotech Financial Statement Overview

Summary
Strong financial inflection with rapid revenue scaling and robust profitability/cash generation in 2024–2025, alongside very low leverage and growing equity. Main offsets are the short track record of sustained profitability and noted data-quality inconsistencies in 2025 margin fields that warrant validation.
Income Statement
86
Very Positive
Revenue scaled sharply from $50.7M (2023) to $290.5M (2024) and $389.1M (2025), with very strong profitability in 2025 (net margin ~52.6% and EBITDA margin ~41.5%). The business has clearly inflected from earlier loss years (2020–2022 had no revenue and sizable losses). Key watch-out: 2025 gross profit and several margin fields appear recorded as zero despite strong earnings, which introduces data-quality noise; additionally, profitability is still relatively new, so investors should expect more volatility than in mature businesses.
Balance Sheet
90
Very Positive
The balance sheet looks conservatively levered with extremely low debt versus equity (debt-to-equity ~0.15% in 2025 and <1% in 2024), and equity has grown materially alongside profitability (equity $1.22B in 2025 vs. $0.95B in 2024). Returns improved meaningfully (return on equity ~16.8% in 2025 vs. ~9.4% in 2024) after negative returns in 2020–2022. Main risk is less about leverage and more about business durability—this is a biotech profile where fundamentals can swing with product/market execution, even if the balance sheet is currently strong.
Cash Flow
88
Very Positive
Cash generation strengthened significantly: operating cash flow rose to $200.9M (2025) from $123.4M (2024), and free cash flow reached $188.9M (2025) from $119.2M (2024). Free cash flow conversion versus net income is solid (~94% in 2025 and ~97% in 2024), suggesting earnings are largely cash-backed. The key weakness is historical volatility—cash flows were meaningfully negative in 2020–2023—so the current strong profile is relatively recent and should be monitored through cycles.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue389.13M290.51M50.70M0.000.00
Gross Profit360.36M270.45M47.60M0.000.00
EBITDA167.85M109.91M-91.32M-116.81M-66.23M
Net Income204.83M89.16M10.93M-139.97M-69.57M
Balance Sheet
Total Assets1.33B1.06B818.36M558.45M626.29M
Cash, Cash Equivalents and Short-Term Investments827.79M597.52M532.18M379.17M438.10M
Total Debt9.34M7.26M8.09M8.93M8.02M
Total Liabilities114.23M109.46M39.71M36.22M32.72M
Stockholders Equity1.22B946.38M778.64M522.23M593.58M
Cash Flow
Free Cash Flow188.91M119.18M-100.60M-153.55M-116.27M
Operating Cash Flow200.87M123.42M-88.80M-100.57M-47.94M
Investing Cash Flow-58.42M-163.44M82.64M-114.08M-226.77M
Financing Cash Flow8.71M27.01M202.75M35.35M347.69M

Krystal Biotech Technical Analysis

Technical Analysis Sentiment
Positive
Last Price272.50
Price Trends
50DMA
265.48
Positive
100DMA
233.74
Positive
200DMA
188.97
Positive
Market Momentum
MACD
1.07
Positive
RSI
51.04
Neutral
STOCH
40.97
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For KRYS, the sentiment is Positive. The current price of 272.5 is below the 20-day moving average (MA) of 273.75, above the 50-day MA of 265.48, and above the 200-day MA of 188.97, indicating a neutral trend. The MACD of 1.07 indicates Positive momentum. The RSI at 51.04 is Neutral, neither overbought nor oversold. The STOCH value of 40.97 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for KRYS.

Krystal Biotech Risk Analysis

Krystal Biotech disclosed 75 risk factors in its most recent earnings report. Krystal Biotech reported the most risks in the "Legal & Regulatory" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Krystal Biotech Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
81
Outperform
$7.80B39.8118.91%54.51%275.94%
66
Neutral
$5.51B21.6814.72%1.08%3.40%
65
Neutral
$5.71B8.7697.54%
55
Neutral
$1.30B-5.17-60.51%-157.74%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
47
Neutral
$5.45B-8.47-30.18%-81.10%-99.21%
40
Underperform
$6.58B-29.03-47.18%-76.96%-425.41%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
KRYS
Krystal Biotech
272.50
99.15
57.20%
ALKS
Alkermes
31.04
-3.00
-8.81%
PTCT
PTC Therapeutics
67.76
17.19
33.99%
CRSP
Crispr Therapeutics AG
55.20
11.58
26.55%
MLTX
MoonLake Immunotherapeutics
18.22
-23.55
-56.38%
ACLX
Arcellx Inc
113.76
52.37
85.31%

Krystal Biotech Corporate Events

Business Operations and StrategyFinancial Disclosures
Krystal Biotech outlines rare disease growth strategy update
Positive
Jan 12, 2026

On January 11, 2026, Krystal Biotech reported selected preliminary, unaudited 2025 results and a strategic business update ahead of its presentation at the 44th Annual J.P. Morgan Healthcare Conference, highlighting that VYJUVEK generated an estimated $106–107 million in net product revenue in the fourth quarter of 2025 and $388–389 million for the full year, with cash, cash equivalents and investments of about $955 million as of December 31, 2025. Management outlined an aggressive rare disease growth strategy built on its HSV-1 platform, including plans to accelerate development of key pipeline candidates KB803, KB801, KB407 and KB111, expand VYJUVEK’s global footprint, and pursue at least four marketed rare disease medicines treating more than 10,000 patients by 2030, while maintaining profitability and investing in larger indications such as alpha-1 antitrypsin deficiency and non-small cell lung cancer, signaling confidence in sustained growth and a multibillion-dollar opportunity set for investors and stakeholders.

The most recent analyst rating on (KRYS) stock is a Buy with a $310.00 price target. To see the full list of analyst forecasts on Krystal Biotech stock, see the KRYS Stock Forecast page.

Business Operations and StrategyProduct-Related AnnouncementsRegulatory Filings and Compliance
Krystal Biotech advances KB407 with positive CF trial data
Positive
Jan 8, 2026

On January 8, 2026, Krystal Biotech reported positive interim results from the highest-dose cohort of its Phase 1 CORAL-1 study of KB407 in cystic fibrosis patients, confirming successful delivery and expression of wild-type CFTR protein in conducting airway cells via inhalation across both modulator-eligible and modulator-ineligible patients, with 29.4% to 42.1% of conducting airway cells transduced in those with successful bronchoscopies and all suitable biopsies showing CFTR or viral marker expression. KB407 was generally well tolerated at the highest dose, with adverse events mostly mild to moderate and one procedure-related serious adverse event resolving within five days, and, on the back of these molecular and safety findings, Krystal has submitted the design of its repeat-dosing, registrational-intent CORAL-3 study to the FDA, targeting alignment on the protocol in early 2026 and enrollment beginning in the first half of 2026, a step that could significantly advance its competitive position in CF gene therapy and offer a potential disease-modifying option for patients who cannot benefit from current modulators.

The most recent analyst rating on (KRYS) stock is a Buy with a $309.00 price target. To see the full list of analyst forecasts on Krystal Biotech stock, see the KRYS Stock Forecast page.

Executive/Board Changes
Krystal Biotech announces resignation of longtime board member
Neutral
Dec 23, 2025

On December 22, 2025, Krystal Biotech announced that board member Kirti Ganorkar had submitted his resignation from the company’s Board of Directors, effective December 31, 2025. Ganorkar, who has served on the board since Krystal’s public listing in September 2017, is stepping down due to time constraints following his recent promotion to Managing Director at Sun Pharma, with the company emphasizing that his departure is not related to any disagreement over its operations, policies, or practices and publicly thanking him for his years of service and contributions.

The most recent analyst rating on (KRYS) stock is a Buy with a $278.00 price target. To see the full list of analyst forecasts on Krystal Biotech stock, see the KRYS 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 18, 2026