CRISPR Therapeutics AG is a leading biotechnology company known for its revolutionary gene-editing technology. The company's values lie in the belief that genetic diseases can be treated and cured using CRISPR-Cas9, a precise and efficient gene-editing tool. With a commitment to improving patients' lives, CRISPR Therapeutics AG aims to develop transformative therapies for multiple genetic disorders. Their corporate philosophy centers around innovation, dedication to scientific advancements, and collaboration with partners to ensure the rapid translation of their technology into potential treatments. Through their cutting-edge research and development, CRISPR Therapeutics AG strives to make significant contributions to the field of gene editing and ultimately bring hope to patients worldwide.

CRISPR Therapeutics AG is primarily present in various countries and regions around the world. The company operates from its headquarters in Basel, Switzerland, providing its groundbreaking gene-editing technology globally. CRISPR Therapeutics AG has a strong presence in the United States, with research and development facilities located in Cambridge, Massachusetts. Additionally, the company has expanded its reach to other regions, including Europe and Asia. With its focus on developing transformative therapies using CRISPR-Cas9 gene-editing technology, CRISPR Therapeutics AG continues to collaborate with partners across the globe to bring innovative treatments to patients in need.

CRISPR Therapeutics AG has reached several significant milestones in its journey. The company successfully initiated clinical trials for the treatment of beta-thalassemia and sickle cell disease using CRISPR-Cas9 gene editing technology. This groundbreaking approach holds great promise in revolutionizing the field of genetic medicine. Additionally, CRISPR Therapeutics AG entered into strategic collaborations with various pharmaceutical companies to develop novel therapeutics for a wide range of diseases. Moreover, the company obtained Fast Track Designation from the U.S. FDA for its CTX001 therapy, further validating its innovative approach and potential impact on patients' lives. CRISPR Therapeutics AG continues to make remarkable progress in advancing gene editing therapies for various genetic disorders.

CRISPR Therapeutics AG is a biopharmaceutical company headquartered in Switzerland. Founded in 2013, the company focuses on developing transformative gene-based medicines using its proprietary CRISPR/Cas9 gene-editing platform. CRISPR Therapeutics AG aims to provide treatments for a wide range of diseases with unmet medical needs. Since its inception, CRISPR Therapeutics AG has made significant advancements in the field of gene editing. The company has forged numerous collaborations with leading pharmaceutical companies to accelerate the development and commercialization of potential therapies. With a robust pipeline and a team of dedicated scientists, CRISPR Therapeutics AG continues to drive innovation in the realm of precision medicine. As a leader in gene-editing technology, CRISPR Therapeutics AG remains committed to improving patients' lives through its groundbreaking research and development efforts.

The main competitors of CRISPR Therapeutics AG in the market are Editas Medicine, Inc., Intellia Therapeutics, Inc., and Sangamo Therapeutics, Inc.

CRISPR Therapeutics AG is primarily active in the biotechnology industry.

The business model of CRISPR Therapeutics AG is focused on developing transformative gene-based medicines using its proprietary CRISPR/Cas9 gene-editing platform. The company aims to address a wide range of severe diseases by leveraging the potential of CRISPR technology to correct genetic defects. CRISPR Therapeutics AG collaborates with various partners to advance its pipeline of therapeutic candidates, spanning areas like hematology, oncology, ophthalmology, and regenerative medicine. Their goal is to bring novel and curative treatments to patients with unmet medical needs. CRISPR Therapeutics AG prioritizes innovation, strategic alliances, and continuous research to drive the advancement of gene-based therapies.

CRISPR Therapeutics의 P/E 비율은 -7.84입니다.

CRISPR Therapeutics의 P/S 비율은 74.15입니다.

CRISPR Therapeutics에 대한 AlleAktien 품질 점수는 2/10입니다.

예상되는 CRISPR Therapeutics 매출은 52.02 백만 USD입니다.

예상되는 CRISPR Therapeutics 이익은 -491.84 백만 USD입니다.

CRISPR Therapeutics AG is a biopharmaceutical company focused on the discovery and development of therapies for genetic diseases. The company uses the innovative CRISPR/Cas9 technology to make specific changes in the human genome and treat hereditary diseases. Its business model is based on researching and applying this technology to develop therapeutics for genetic diseases. CRISPR Therapeutics has a wide pipeline of products at various stages of development, from preclinical to clinical phase III. The company has an exclusive license for the therapeutic use of CRISPR/Cas9 technology from the University of California, Berkeley and the Massachusetts Institute of Technology (MIT). It has also formed a strategic alliance with Vertex Pharmaceuticals to develop new therapies for lysosomal storage diseases. One of the key products being developed by CRISPR Therapeutics is CTX001, a gene therapy for the treatment of beta-thalassemia and sickle cell disease. This therapy uses CRISPR/Cas9 to modify the patient's blood stem cells to increase the production of fetal hemoglobin and replace the defective hemoglobin. CTX001 is currently in clinical phase III development and is being jointly developed by CRISPR Therapeutics and Vertex Pharmaceuticals. Additionally, CRISPR Therapeutics is developing therapies for other genetic diseases such as hemophilia A, Duchenne muscular dystrophy, and cystic fibrosis. This is achieved by targeting disease-causing genes and using CRISPR/Cas9 to regulate gene expression. The company's business model also includes licensing its technology to other companies for the development of therapies for other diseases. It has partnered with Bayer to develop therapies for the treatment of blood and liver diseases. Overall, CRISPR Therapeutics has an innovative business model based on the use of CRISPR/Cas9 technology to make specific changes in the human genome and treat or cure genetic diseases. Through the development of CTX001 and other therapies, the company has significant potential to improve the lives of patients with genetic diseases.

CRISPR Therapeutics은(는) 연간 번의 배당을 통해 0 USD의 배당금을 지급합니다.

CRISPR Therapeutics의 현재 배당금은 계산할 수 없거나, 회사가 배당금을 지급하지 않습니다.

CRISPR Therapeutics의 ISIN은 CH0334081137입니다.

CRISPR Therapeutics의 WKN은 A2AT0Z입니다.

CRISPR Therapeutics의 티커는 CRSP입니다.

지난 12개월 동안 CRISPR Therapeutics은(는) 의 배당금을 지급했습니다. 이는 약 의 배당 수익률에 해당합니다. 향후 12개월 동안 CRISPR Therapeutics은(는) 0 USD의 배당금을 지급할 것으로 예상됩니다.

CRISPR Therapeutics의 현재 배당 수익률은 입니다.

CRISPR Therapeutics은 분기별로 배당금을 지급합니다. 이는 월에 배당됩니다.

CRISPR Therapeutics은(는) 지난 0년 동안 매년 배당금을 지급했습니다.

향후 12개월 동안 0 USD의 배당금이 예상됩니다. 이는 배당수익률 0 %에 해당합니다.

CRISPR Therapeutics은 '건강' 섹터에 속합니다.

CRISPR Therapeutics의 마지막 배당금을 0 USD만큼 받기 위해선 의 Ex-Tag 전에 주식을 보유하고 있어야 했습니다.

마지막 배당금 지급일은 입니다.

2023년에 CRISPR Therapeutics는 0 USD를 배당금으로 지급했습니다.

CRISPR Therapeutics의 배당금은 USD에 지급됩니다.