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Forecast
The analysts' average price target is €56.17 (+20.82%). The median is €51.57 (+10.93%).
| Buy |
Â
22 |
| Hold |
Â
14 |
| Sell |
Â
2 |
News Go to news feed
CRISPR Therapeutics presents pipeline expansion and commercial progress at Morgan Stanley conference
CRISPR Therapeutics presented progress on commercialization of CASGEVY and a broadening development pipeline at the Morgan Stanley Global Healthcare Conference. Vertex reported about $76 million in quarterly revenue for CASGEVY and more than 100 new treatments per quarter; management sees potential for annualized revenue well above $500 million and long-term up to $1 billion. Key programs with data expected by the end of 2026 include CTX310 (cardiovascular risk), CTX611 (Factor XI anticoagulation) and Zugo-cel (allogeneic CAR‑T for autoimmune diseases); additional early programs are slated to deliver initial data in early 2027. The company emphasizes sufficient funding to self-finance the pipeline, the use of AI to accelerate R&D, and a long-term strategy toward in vivo editing and gene insertion. » More on de.investing.com
CRISPR Therapeutics shows positive one-year data for gene therapy CTX310
A single IV infusion of CTX310 at the highest dose produced after one year a median reduction in ANGPTL3 of 79%, triglycerides of 48% and LDL of 53% versus baseline; maximum reductions were 89% (ANGPTL3), 78% (triglycerides) and 84% (LDL). The phase‑1a dose‑escalation study with 15 participants showed no dose‑limiting toxicities or serious treatment‑related adverse events; three grade‑2 infusion reactions resolved and a transient liver value increase was observed. CRISPR is continuing CTX310 in a phase‑1b fixed‑dose 0.8 mg/kg study and expects an update in the second half of 2026, focusing on patients with severe hypertriglyceridemia. » More on de.investing.com
CRISPR Therapeutics posts revenue growth, advances pipeline while Ark remains heavily invested
CRISPR Therapeutics has seen modest stock gains this year but reported Q2 revenue rising to $10.2 million, narrower losses and a stronger cash position of $2.36 billion. Its commercial therapy Casgevy is driving revenue and received FDA approval for children aged 2 and up, potentially expanding the addressable market, while pipeline programs including CTX611 and off-the-shelf CAR-T candidates CTX112/CTX131 progress toward later-stage trials. Cathie Wood's Ark Invest holds 94.6 million shares at an average cost of $66, leaving the fund below breakeven at current prices, but the company says its improving finances could fund multiple upcoming clinical readouts. » More on finance.yahoo.com
Financials
| (EUR) | September 2026 | YoY |
|---|---|---|
| Revenue | 11.18m | 1,376.46% |
| Gross profit | -114.81m | 111.17% |
| Net profit | -98.38m | 8.47% |
| EBITDA | -94.58m | 9.47% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €4.3bn |
Number of shares | 96.69m |
52-week high/low | €56.42 - €39.23 |
| Dividends | No |
Beta | 1.90 |
P/E ratio | -10.55 |
PEG ratio | -1.30 |
P/B ratio | 2.93 |
P/S ratio | 192.03 |
Company profile
CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious diseases using its proprietary Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. Its CRISPR/Cas9 is a gene editing technology that allows for precise directed changes to genomic DNA. The company has a portfolio of therapeutic programs across a range of disease areas, including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company's lead product candidate is CTX001, an ex vivo CRISPR gene-edited therapy for treating patients suffering from transfusion-dependent beta-thalassemia or severe sickle cell disease in which a patient's hematopoietic stem cells are engineered to produce high levels of fetal hemoglobin in red blood cells. It also develops CTX110, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting cluster of differentiation 19 positive malignancies; CTX120, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting B-cell maturation antigen for the treatment of relapsed or refractory multiple myeloma; and CTX130, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting Cluster of Differentiation 70 to treat various solid tumors and hematologic malignancies. In addition, the company develops VCTX210, a gene-edited immune-evasive stem cell-derived product candidate for the treatment of treatment of type 1 diabetes; and pursues various in vivo gene-editing programs that target the liver, lung, muscle, and central nervous system diseases. It has strategic partnerships with Bayer Healthcare LLC, Vertex Pharmaceuticals Incorporated, ViaCyte, Inc., Nkarta, Inc., and Capsida Biotherapeutics. CRISPR Therapeutics AG was incorporated in 2013 and is headquartered in Zug, Switzerland.
| Name | CRISPR Therapeutics |
| CEO | Samarth Kulkarni |
| Headquarters | Zug,
zg Switzerland |
| Website | |
| Sector | Health Care |
| Industry | Biotechnology |
| IPO | 19/10/2016 |
| Employees | 393 |
Ticker symbols
| Exchange | Symbol |
|---|---|
NASDAQ | CRSP |
DĂĽsseldorf | 1CG.DU |
London | 0VRQ.L |
SIX | 1CG.SW |
MĂĽnchen | 1CG.MU |
Frankfurt | 1CG.F |