CRISPR Therapeutics AG Share Price & Technical Analysis

CRSP · $50.36 (+0.92%)

Healthcare / Biotechnology

AI Score 25 · Bearish

$50.36

+0.92%

CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious human diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. The company's CRISPR/Cas9 is a technology for gene editing which is the process of precisely altering specific sequences of genomic DNA. It has a portfolio of t

Price chart

Seasonality

May has 3 positive and 2 negative years (last 5 years shown)

-2% return in May, 9% avg return in past 3 year May month.

5% return in 2026, 23% avg return in past 3 years.

Swipe sideways to see all months →

JanFebMarAprMayJunJulAugSepOctNovDecYr
26-5%21%-18%9%-2%5%
255%9%-25%14%-6%32%16%-5%27%-1%-15%0%52%
242%33%-19%-22%1%-1%6%-17%-1%-1%9%-23%-34%
2324%-4%-8%8%31%-12%2%-12%-10%-14%53%-5%51%
22-17%-6%4%-22%17%5%23%-12%2%-21%2%-25%-50%

Monthly return % by calendar month · historical pattern, not a forecast

AI snapshotScore 25/100

Bearish · Downtrend · Neutral

CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious human diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. The company's CRISPR/Cas9 is a technology for gene editing which is the process of precisely altering specific sequences of genomic DNA. It has a portfolio of therapeutic programs across a range of disease areas, including hemoglobinopathies, CAR T cell therapies, in vivo, and type 1 diabetes, as well as develops investigational CAR T programs, including an autologous, gene-edited CAR T program targeting allogeneic chimeric antigen receptor T cell for autoimmune indications and oncology. The company's lead product candidate is CASGEVY, an ex vivo CRISPR/Cas9 gene-edited cell therapy for treating patients suffering from transfusion-dependent beta-thalassemia, severe sickle cell disease (SCD), and hemoglobinopathies in which a patient's hematopoietic stem and progenitor cells are edited to produce high levels of fetal hemoglobin in red blood cells. It also develops CAR T cell therapies, including CTX112 targeting cluster of differentiation 19 (CD19) and CTX131 targeting CD70 for oncology and autoimmune indications; CTX310 and CTX320, in vivo gene editing to address the cardiovascular disease by disrupting the validated targets angiopoietin-like protein 3 and lipoprotein; and CTX211, an allogeneic, gene-edited, hypoimmune stem cell-derived product candidate for the treatment of T1D. It has strategic partnerships with Vertex Pharmaceuticals Incorporated. CRISPR Therapeutics AG was incorporated in 2013 and is headquartered in Zug, Switzerland.

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Key metrics

Market cap

$5.04B

P/E ratio

52W high

$78.48

52W low

$35.38

Volume

15,50,761

Beta

1.74

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