CRISPR Therapeutics Logo
CH0334081137
A2AT0Z
CRSP

CRISPR Therapeutics

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Forecast

The analysts' average price target is €56.17 (+20.82%). The median is €51.57 (+10.93%).

Buy
  22
Hold
  14
Sell
  2

  • 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

In the last quarter, CRISPR Therapeutics had revenue of €11.18m and net profit of -€98.38m
(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
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