CRISPR Therapeutics Option Alert: Jan 16 $55 Calls Sweep (35) near the Bid: 449 vs 3024 OI; Earnings 11/4 Before Open [est] 

CRISPR Therapeutics Option Alert: Jan 16 $55 Calls Sweep (35) near the Bid: 449 @ $14.101 vs 3024 OI; Earnings 11/4 Before Open [est] Ref=$65.27

CRISPR Therapeutics

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 first approved drug is Casgevy, which was developed in collaboration with Vertex Pharmaceuticals and targets sickle-cell disease and transfusion-dependent beta-thalassemia, which have high unmet medical needs. The company is advancing a variety of gene editing programs in immuno-oncology, cardiovascular, and a stem cell-derived therapy to treat Type 1 diabetes.

Cathie Wood's ARKK

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ARKK supera al Nasdaq con entradas récord y un rally basado en beneficios reales e innovación tecnológica.

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TIME revela las 100 empresas más influyentes de 2025. Conoce las compañías en bolsa que lideran innovación y crecimiento este año.

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Cathie Wood señala dos acciones biotecnológicas con potencial de crecimiento explosivo gracias a la revolución genética y la IA.

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CRISPR Therapeutics AG

Press Releases

CRISPR Therapeutics Named to TIME's Most Influential Companies List of 2025

Small Caps, Big Potential: Regenerative Medicine Stocks Positioned for Growth

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Breaking Through: Systemic Genetic Medicines for Hard-to-Treat Cancers

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CRISPR Therapeutics Provides Business Update and Reports Second Quarter 2025 Financial Results

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CRISPR Therapeutics to Participate in Upcoming Investor Conferences

CRISPR Therapeutics to Present Late-Breaking Data at the American Heart Association (AHA) Scientific Sessions 2025

Global Cell Therapy Market Size Expected to Reach $44 Billion as Demand for Regenerative Medicine Rises

General

CRISPR Therapeutics and Sirius Therapeutics Announce First Patient Dosed in Phase 2 Trial of SRSD107 for Thromboembolic Disorders in Europe

CRISPR Therapeutics to Present Preclinical Data on Alpha-1 Antitrypsin Deficiency (AATD) Utilizing Novel SyNTase Gene Editing Technology at the European Society of Gene and Cell Therapy (ESGCT) 2025 Annual Congress

Australia's Largest University Establishes 'Monash Boston Hub' to Accelerate Global Biotech Partnerships and Licensing

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CRISPR Therapeutics

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