CRISPR Therapeutics AG (CRSP) Stock Price & How to Invest
Last updated July 2026
Short answer
You can invest in CRISPR Therapeutics (CRSP) by buying shares or fractional shares at any major broker, through an ETF that holds it, or as one holding in a thematic basket. CRSP is the only CRISPR-focused biotech that has advanced beyond clinical-stage development, having co-developed Casgevy, the world's first approved CRISPR-based gene therapy, with partner Vertex Pharmaceuticals. The company's bull case rests on Casgevy's gradual commercial ramp in sickle cell disease and beta-thalassemia, plus a pipeline spanning next-generation CAR-T therapies, in vivo cardiovascular gene editing, and newly acquired siRNA assets. The single biggest risk is that Casgevy's adoption has been very slow and costly to scale, the company posted a 2025 operating loss of roughly $665 million, and it must also repay approximately $222 million in previously deferred program costs before seeing meaningful net cash inflows from its lead product.
CRSP stock price
As of 2026-07-31, CRISPR Therapeutics AG (CRSP) last closed at $47.99, down 14.4% over the past year. Over the past 52 weeks it has traded between $44.34 and $76.78.
Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or CRISPR Therapeutics AG's investor relations page. Walnut is informational, not investment advice.
What does CRISPR Therapeutics AG (CRSP) do?
CRISPR Therapeutics AG is a Swiss-American biopharmaceutical company headquartered in Zug, Switzerland, with principal research operations in Boston, Massachusetts. The company uses its proprietary CRISPR/Cas9 platform to develop gene-based medicines across hemoglobinopathies, oncology, cardiovascular disease, autoimmune conditions, and regenerative medicine. Its first and only commercialized product, Casgevy, is co-developed and co-commercialized with Vertex Pharmaceuticals under a 40/60 profit-sharing structure in which CRISPR retains 40 percent of profits. Revenue has historically been driven by collaboration milestone payments from Vertex rather than product sales, making the financial profile highly lumpy. Beyond Casgevy, the company generates no meaningful product revenue today and funds operations through its cash reserves.
CRISPR Therapeutics was founded in 2013 by Emmanuelle Charpentier, a Nobel Prize laureate in Chemistry, alongside Shaun Foy and Rodger Novak. It went public on the Nasdaq in October 2016 and entered a landmark collaboration with Vertex Pharmaceuticals in 2015 that ultimately led to Casgevy's FDA approval in December 2023 for sickle cell disease and in January 2024 for transfusion-dependent beta-thalassemia. The company has been led since December 2017 by CEO and Chairman Samarth (Sam) Kulkarni, a former McKinsey partner with a PhD background who joined in 2015 as Chief Business Officer. Under his leadership the pipeline has expanded into next-generation allogeneic CAR-T programs (CTX112, CTX131), in vivo cardiovascular gene editing (CTX310, CTX320), and in May 2025 the company paid $95 million upfront to acquire CTX611, a clinical-stage siRNA therapy for thrombosis prevention.
What's driving CRISPR Therapeutics AG (CRSP)?
First-Mover Advantage in Commercial Gene Editing
Casgevy is the world's first approved CRISPR-based medicine, giving CRISPR Therapeutics a durable head start in manufacturing know-how, regulatory relationships, and patient community trust. No direct CRISPR competitor has yet reached commercial approval for the same indications. That first-mover status matters because gene therapy infrastructure, including certified treatment centers and payer contracting, takes years to build.
Casgevy's Long-Term Revenue Potential
Sickle cell disease affects an estimated 100,000 patients in the United States alone, and transfusion-dependent beta-thalassemia adds tens of thousands more globally. Analysts have modeled Casgevy's peak annual sales in the billions of dollars if reimbursement access broadens and the treatment process is simplified. Reimbursement agreements are expanding in multiple countries, and Vertex's global commercial infrastructure handles the rollout.
Diversified Pipeline with Blockbuster Potential
Beyond Casgevy, clinical-stage CAR-T programs CTX112 and CTX131 target B-cell malignancies and autoimmune diseases, with broad data updates anticipated in 2025 and 2026. In vivo cardiovascular candidates CTX310 and CTX320 target ANGPTL3 and LPA respectively, addressing large patient populations. The 2025 acquisition of CTX611, a long-acting siRNA therapy silencing Factor XI for thrombosis prevention, further widens the addressable market.
Strong Balance Sheet Providing Operational Runway
CRISPR Therapeutics closed 2025 with approximately $1.98 billion in liquidity, which management states is sufficient to fund operations for at least 24 months. That cash cushion means the company is unlikely to need emergency dilutive financing in the near term, giving the pipeline time to generate clinical data. A subsequent convertible notes offering in early 2026 supplemented the position further.
What are the risks to CRISPR Therapeutics AG (CRSP)?
The commercial ramp of Casgevy has been far slower than early projections, with the therapy generating only approximately $3.5 million in revenue in all of 2025, down sharply from prior years that were boosted by one-time milestone payments. The expiration of CRISPR's cost-deferral agreement with Vertex drove collaboration expenses up roughly 77 percent year over year in 2025, contributing to a full-year operating loss of approximately $665 million, and the company must repay around $222 million in previously deferred costs before net cash flows from Casgevy accrue to CRSP shareholders. Competing gene-editing and cell-therapy platforms from Intellia Therapeutics, Beam Therapeutics, and large pharmaceutical companies pursuing in vivo approaches could erode CRSP's differentiation over time. The stock also carries high short interest, above 22 percent of shares outstanding as of recent data, reflecting meaningful institutional skepticism about the pace of the commercial ramp.
What is the CRISPR Therapeutics AG (CRSP) forecast?
18 analysts publish price targets on CRSP, averaging $86.78 against a $47.99 price as of August 2026, or +80.8%. The published targets run from $44.00 to $291.00, a wide spread, and the ratings split 13 buy, 9 hold, 0 sell. Over the last six months there have been 7 raises and 0 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.
Read the full CRSP forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.
Is CRSP a buy or a sell?
We give no verdict on CRISPR Therapeutics AG. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.
The case for buying. First-Mover Advantage in Commercial Gene Editing. Casgevy is the world's first approved CRISPR-based medicine, giving CRISPR Therapeutics a durable head start in manufacturing know-how, regulatory relationships, and patient community trust. The most optimistic published target, $291.00, assumes this works close to its best case.
The case against. The commercial ramp of Casgevy has been far slower than early projections, with the therapy generating only approximately $3.5 million in revenue in all of 2025, down sharply from prior years that were boosted by one-time milestone payments. The most pessimistic target, $44.00, is roughly what CRSP is worth if this bites instead.
Read the full bull and bear case on CRSP, including what would have to change to break either one. Walnut is not an investment adviser.
How is CRISPR Therapeutics AG (CRSP) valued? (approximate, June 27, 2026 (data reflects most recently available reports through mid-2026))
A simple financial snapshot. These are approximations and refresh quarterly; for current figures see CRISPR Therapeutics AG's investor relations page or your broker.
- Revenue (Full Year 2025, product only): ~$3.5 million
- Revenue (Full Year 2024): ~$37.3 million (primarily collaboration revenue)
- Net Loss (TTM through Q3 2025): ~$488 million
- Operating Loss (Full Year 2025): ~$665 million
- Market Capitalization: ~$4.5 to $5.2 billion (range reflecting recent price movement near $54)
- Cash and Marketable Securities: ~$1.98 billion (as of December 31, 2025)
- P/E Ratio (TTM): Negative (not meaningful; company is unprofitable)
- Short Interest: ~22% of shares outstanding
Because CRISPR Therapeutics has no meaningful product profits yet, traditional earnings-based valuation multiples like P/E are negative and not analytically useful. The company is better evaluated on its cash runway, the pace of Casgevy's commercial adoption, and the risk-adjusted value of its pipeline. Enterprise value of roughly $2.8 billion (market cap less net cash) reflects the market pricing in significant execution uncertainty around both the Casgevy ramp and the broader pipeline, while a wide spread exists between bearish analyst targets near $33 and optimistic targets above $80.
Which ETFs hold CRISPR Therapeutics AG (CRSP)?
What themes does CRISPR Therapeutics AG (CRSP) fit?
These are the investment theses CRSP naturally fits into. Each links to a full theme guide listing every other stock that belongs and the ETFs commonly used as a passive proxy.
Who competes with CRISPR Therapeutics AG (CRSP)?
Pure-Play CRISPR Gene Editing Companies
Intellia Therapeutics (NTLA) and Editas Medicine (EDIT) were founded around the same time as CRISPR Therapeutics and share the same foundational ambition of turning CRISPR science into medicines. Intellia has three Phase 3 programs including lonvoguran ziclumeran for hereditary angioedema and nex-z for ATTR amyloidosis, in collaboration with Regeneron. Editas shuttered its sickle cell program in 2024 and has a significantly weaker financial position. Beam Therapeutics pursues base editing, a CRISPR variant that makes single-nucleotide changes without double-strand DNA breaks, and is advancing programs in sickle cell disease and other areas. None of these peers has yet achieved a commercial drug approval, which currently differentiates CRSP.
Established CAR-T Therapy Developers
CRSP's allogeneic (off-the-shelf) CAR-T programs CTX112 and CTX131 compete in a space already populated by approved autologous CAR-T therapies from Kymriah (Novartis), Yescarta (Gilead/Kite), and Breyanzi (Bristol Myers Squibb). The off-the-shelf approach that CRSP is pursuing promises faster patient access and lower manufacturing cost, but these advantages must be demonstrated in head-to-head clinical and commercial settings against entrenched players with established payer relationships.
Large Pharma with Gene Editing Partnerships
Major pharmaceutical companies including Regeneron (partnered with Intellia), Novartis, and Pfizer have invested in or partnered around gene editing technologies, giving them the potential to enter CRSP's therapeutic areas with far greater commercial infrastructure and balance sheet resources. Vertex Pharmaceuticals is simultaneously CRSP's most important partner for Casgevy and a potential competitive force if its interests diverge from CRISPR's in future program negotiations.
Next-Generation Gene Silencing and Correction Platforms
Companies like Alnylam Pharmaceuticals, with approved RNA interference drugs for rare diseases, and Prime Medicine, pursuing prime editing for precise gene correction, represent platform-level competition for the same patient populations and R&D dollars. Verve Therapeutics is developing single-course in vivo cardiovascular gene editing that directly overlaps with CRSP's CTX310 and CTX320 programs targeting ANGPTL3 and LPA.
What stocks are similar to CRISPR Therapeutics AG (CRSP)?
Other names that sit close to CRSP: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.
How to invest in CRISPR Therapeutics AG (CRSP)
There are three common ways to get CRSP exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it (ARKG, ARKK), which spreads the position across many companies. Or build it into a focused thematic portfolio, so CRSP sits alongside other stocks that express the same thesis.
Walnut takes the portfolio route. Describe a thesis where CRSP fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.
New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.
The bottom line on CRISPR Therapeutics AG (CRSP)
CRISPR Therapeutics is a commercial-stage gene-editing company whose entire near-term financial story hinges on the uptake trajectory of Casgevy, a one-time therapy priced at $2.2 million per patient that generated only about $3.5 million in product revenue in full-year 2025 as the rollout remains in its infancy. If you believe gene editing will become a mainstream treatment modality and that Casgevy's reimbursement coverage will expand meaningfully over the next several years while CRSP's CAR-T and cardiovascular pipeline adds further option value, the question becomes sizing and overlap with other biotech positions, not timing. The risk is that the commercial ramp stalls due to the therapy's complexity, payer pushback, or manufacturing costs, leaving the company burning through its approximately $2 billion cash reserve faster than new revenue can replace it.
More on CRISPR Therapeutics AG (CRSP)
Whether CRSP is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is CRSP a buy or a sell?, and where the stock could go from here in the CRSP stock forecast.
For income investors, whether CRSP pays a dividend and how the payout looks is covered in does CRSP pay a dividend? And to weigh CRSP against a peer, read the full side-by-side comparisons: CRSP vs VRTX and CRSP vs REGN.
Wondering how CRSP fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.
Investing in CRISPR Therapeutics AG with AI
Connect the broker you already use and ask Walnut's AI how CRSP fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.
FAQ
What does CRISPR Therapeutics do?
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CRISPR Therapeutics uses its CRISPR/Cas9 gene editing platform to develop medicines for serious diseases. Its only approved product is Casgevy, co-developed with Vertex Pharmaceuticals, which is the world's first CRISPR-based therapy and targets sickle cell disease and transfusion-dependent beta-thalassemia. Its pipeline spans CAR-T cancer therapies, cardiovascular gene editing, and an acquired siRNA program.
Is CRSP a good stock to buy right now?
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That depends entirely on an investor's risk tolerance and time horizon. CRSP offers exposure to a genuinely first-of-its-kind commercial gene-editing asset and a broad pipeline, but the company is deeply unprofitable, burning several hundred million dollars per year, with Casgevy's commercial ramp proving very slow. Analysts hold widely divergent views, with price targets ranging from around $33 to over $80.
Does CRSP pay a dividend?
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No. CRISPR Therapeutics does not pay a dividend. The company is pre-profitability with significant annual operating losses, and its capital is directed entirely toward clinical development and the commercial rollout of Casgevy. Investors seeking income from dividends would need to look elsewhere in the biotech or broader healthcare sector.
Who are CRISPR Therapeutics's main competitors?
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The most direct pure-play competitors are Intellia Therapeutics (NTLA), Editas Medicine (EDIT), and Beam Therapeutics, all of which pursue CRISPR or related gene editing platforms. In CAR-T therapies, CRSP competes with Novartis, Gilead/Kite, and Bristol Myers Squibb. In cardiovascular gene editing, Verve Therapeutics targets overlapping programs. Large pharma companies with gene-editing partnerships represent longer-term competitive threats.
Is CRSP overvalued?
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Valuation is genuinely contested. With a market cap of roughly $4.5 to $5.2 billion and near-zero product revenue, traditional multiples like P/E are not meaningful. Bears argue the stock prices in an optimistic Casgevy ramp that has not materialized. Bulls counter that the enterprise value net of cash is a reasonable option price on a multi-product gene-editing platform. Neither view is obviously wrong, and the answer depends heavily on Casgevy adoption assumptions.
What is Casgevy and why does it matter?
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Casgevy is the world's first approved CRISPR-based gene therapy, co-developed by CRISPR Therapeutics and Vertex Pharmaceuticals. It received FDA approval for sickle cell disease in December 2023 and for transfusion-dependent beta-thalassemia in January 2024. Priced at $2.2 million per patient, it represents a potential one-time functional cure but faces challenges around patient access, payer coverage, and the complex treatment process.
How much cash does CRISPR Therapeutics have?
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As of December 31, 2025, CRISPR Therapeutics reported approximately $1.98 billion in cash, cash equivalents, and marketable securities, which management stated is sufficient to fund operations for at least 24 months. A subsequent convertible notes offering in early 2026 added to that position. This runway is a key reason the company is not considered at immediate risk of needing emergency dilutive financing.
What is the biggest risk of investing in CRSP?
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The biggest risk is that Casgevy's commercial adoption remains far slower than projected while operating losses, now exceeding $600 million annually, continue to erode the cash reserve. The therapy's high price, complex treatment process requiring hospitalization, and the burden of repaying approximately $222 million in previously deferred partner costs all weigh on the timeline to profitability. Pipeline setbacks in CAR-T or cardiovascular programs would compound the risk.
Guides that feature CRSP
CRSP is one of the names covered in these guides. Each one puts the stock next to its peers so you can see where it fits rather than judging it alone.
Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with CRISPR Therapeutics AG's investor relations page or your broker before making investment decisions.