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CRISPR Therapeutics AG (MEX:CRSP) Institutional Ownership : 61.07% (As of Jun. 23, 2024)


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What is CRISPR Therapeutics AG Institutional Ownership?

Institutional ownership is the percentage of shares that are owned by institutions out of the total shares outstanding. As of today, CRISPR Therapeutics AG's institutional ownership is 61.07%.

Insider Ownership is the percentage of shares that are owned by company insiders relative to the total shares outstanding. As of today, CRISPR Therapeutics AG's Insider Ownership is 0.00%.

Float Percentage Of Total Shares Outstanding is the percentage of float shares relative to the total shares outstanding. As of today, CRISPR Therapeutics AG's Float Percentage Of Total Shares Outstanding is 88.17%.


CRISPR Therapeutics AG Institutional Ownership Historical Data

The historical data trend for CRISPR Therapeutics AG's Institutional Ownership can be seen below:

* For Operating Data section: All numbers are indicated by the unit behind each term and all currency related amount are in USD.
* For other sections: All numbers are in millions except for per share data, ratio, and percentage. All currency related amount are indicated in the company's associated stock exchange currency.

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CRISPR Therapeutics AG Institutional Ownership Chart

CRISPR Therapeutics AG Historical Data

The historical data trend for CRISPR Therapeutics AG can be seen below:

2023-08-31 2023-09-30 2023-10-31 2023-11-30 2023-12-31 2024-01-31 2024-02-29 2024-03-31 2024-04-30 2024-05-31
Institutional Ownership 64.30 64.38 63.94 64.14 65.04 63.63 64.56 61.51 60.89 61.07

CRISPR Therapeutics AG Institutional Ownership Calculation

The percentage of shares that are owned by institutions out of the total shares outstanding.


CRISPR Therapeutics AG (MEX:CRSP) Business Description

Traded in Other Exchanges
Address
Baarerstrasse 14, Zug, CHE, CH-6300
CRISPR Therapeutics is a gene editing company focused on the development of CRISPR/Cas9-based therapeutics. CRISPR/Cas9 stands for Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9), which is a revolutionary technology for precisely altering specific sequences of genomic DNA. The company is focused on using this technology to treat genetically defined diseases. CRISPR's most advanced pipeline candidate, exa-cel, is in collaboration with Vertex Pharmaceuticals and targets sickle cell disease and transfusion-dependent beta-thalassemia, which have high unmet medical needs. The company is progressing additional gene editing programs for immuno-oncology, as well as a stem cell-derived therapy for the treatment of Type 1 diabetes.