CRISPR Therapeutics AG
NASDAQ:CRSP
CRSP's latest stock split occurred on Jul 19, 2016
The company executed a 333333-for-100000 stock split, meaning that for every 100000 shares held, investors received 333333 new shares.
The adjusted shares began trading on Jul 19, 2016. This was the only stock split in CRSP's history.
WTO
CRISPR Therapeutics AG
Glance View
CRISPR Therapeutics AG is at the forefront of revolutionizing modern medicine through gene-editing technology. Founded on the groundbreaking research of CRISPR-Cas9, a tool that allows scientists to precisely alter an organism’s DNA, the company has swiftly emerged as a leader in the biotech arena. Situated in Switzerland, with significant operations in the United States, CRISPR Therapeutics aims to translate this cutting-edge science into transformative therapies. Its portfolio highlights collaborative efforts with other industry giants to develop treatments for serious genetic diseases, such as its flagship program targeting sickle cell disease and beta-thalassemia. By leveraging its proprietary CRISPR platform, the company focuses on developing gene-based medicines that address the root causes of illnesses, marking a departure from traditional symptom management to potentially groundbreaking cures. The business model of CRISPR Therapeutics is both innovative and strategic. Monetization is achieved through a blend of partnerships, licensing agreements, and direct therapeutic development. The company collaborates with various pharmaceutical entities, creating a network of shared knowledge and resources that accelerates the commercialization of therapies. These alliances facilitate shared risk and reward, allowing CRISPR Therapeutics to generate revenue while advancing its research and development pipeline. Moreover, the successful progression of any internally-developed therapies into approved treatments has the potential to unlock significant financial returns, both from sales and potential royalties. True to its visionary roots, CRISPR Therapeutics not only pursues immediate financial success but also seeks to redefine the landscape of genetic medicine with the long-term goal of delivering curative treatments for numerous genetic conditions.
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