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Crispr Therapeut - CRSP STOCK NEWS

Welcome to our dedicated page for Crispr Therapeut news (Ticker: CRSP), a resource for investors and traders seeking the latest updates and insights on Crispr Therapeut stock.

CRISPR Therapeutics AG (symbol: CRSP) is a pioneering gene editing company dedicated to the development of transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. This revolutionary technology allows for precise, directed changes to genomic DNA, enabling the treatment of genetically defined diseases.

The company's portfolio spans a broad range of therapeutic programs, including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. One of its notable achievements is the development and approval of Casgevy, a therapeutic targeting sickle cell disease and transfusion-dependent beta-thalassemia, developed in collaboration with Vertex Pharmaceuticals.

To bolster its research and development, CRISPR Therapeutics has forged strategic partnerships with renowned companies such as Bayer, Vertex Pharmaceuticals, and ViaCyte, Inc. These collaborations aim to accelerate and expand the company's efforts in bringing novel therapies to market.

Headquartered in Zug, Switzerland, CRISPR Therapeutics operates through its wholly-owned U.S. subsidiary, with R&D operations based in Cambridge, Massachusetts, and business offices in San Francisco, California, and London, United Kingdom.

The company's ongoing projects include advancing gene editing programs in immuno-oncology and developing stem cell-derived therapies for the treatment of Type 1 diabetes. With its innovative approach and strategic collaborations, CRISPR Therapeutics is at the forefront of the gene editing revolution, poised to make significant impacts in the field of medicine.

For more information, please visit www.crisprtx.com.

Rhea-AI Summary
CRISPR Therapeutics completes Advisory Committee meeting for exa-cel for severe sickle cell disease (SCD) and assigns Prescription Drug User Fee Act (PDUFA) target action dates for SCD and transfusion-dependent beta thalassemia (TDT). Ongoing clinical trials for CAR T product candidates targeting B-cell malignancies, T cell malignancies and solid tumors. Also, clinical trials ongoing for VCTX211 for Type 1 Diabetes and CTX310 targeting angiopoietin-related protein 3 (ANGPTL3).
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CRISPR Therapeutics announces preclinical data from investigational programs for cardiovascular disease treatment. CTX310™ shows durable reductions in ANGPTL3 protein and triglyceride levels in non-human primates after a single dose. CTX320™ shows durable reductions in lipoprotein(a) levels in non-human primates after a single dose. Clinical trial initiated for CTX310™, targeting ANGPTL3. CTX320™ targeting Lp(a) is on track to enter the clinic in the first half of 2024.
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CRISPR Therapeutics announced the completion of the FDA's advisory committee meeting for exa-cel, a potential therapy for severe sickle cell disease (SCD). The PDUFA target action date for SCD is December 8, 2023. If approved, exa-cel could be the first genetic therapy available to approximately 20,000 people with severe SCD in the U.S. The BLA for transfusion-dependent beta-thalassemia (TDT) has a PDUFA date of March 30, 2024.
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CRISPR Therapeutics (Nasdaq: CRSP) announces trading halt as FDA reviews Biologics License Application for exagamglogene autotemcel (exa-cel) for sickle cell disease treatment.
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CRISPR Therapeutics announces poster presentations of preclinical data at SITC 38th Annual Meeting.
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CRISPR Therapeutics co-founder, Rodger Novak, M.D., to step down as President and Chairman, effective September 15, 2023
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CRISPR Therapeutics to participate in fireside chat at Citi's Biopharma Conference
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FAQ

What is the current stock price of Crispr Therapeut (CRSP)?

The current stock price of Crispr Therapeut (CRSP) is $44.51 as of February 25, 2025.

What is the market cap of Crispr Therapeut (CRSP)?

The market cap of Crispr Therapeut (CRSP) is approximately 4.0B.

What is CRISPR Therapeutics AG?

CRISPR Therapeutics AG is a gene editing company focused on developing transformative gene-based medicines using its proprietary CRISPR/Cas9 platform.

What does the CRISPR/Cas9 platform do?

CRISPR/Cas9 is a revolutionary gene editing technology that enables precise, directed changes to genomic DNA, allowing for the treatment of genetically defined diseases.

Where is CRISPR Therapeutics headquartered?

CRISPR Therapeutics is headquartered in Zug, Switzerland, with additional offices in the U.S. and the UK.

What is Casgevy?

Casgevy is a therapeutic developed by CRISPR Therapeutics in collaboration with Vertex Pharmaceuticals, targeting sickle cell disease and transfusion-dependent beta-thalassemia.

What types of diseases is CRISPR Therapeutics targeting?

CRISPR Therapeutics is targeting a range of diseases including hemoglobinopathies, oncology, regenerative medicine, and rare diseases.

Who are CRISPR Therapeutics' key partners?

CRISPR Therapeutics has established strategic collaborations with companies like Bayer, Vertex Pharmaceuticals, and ViaCyte, Inc.

What are some of CRISPR Therapeutics' current projects?

Current projects include advancing gene editing programs for immuno-oncology and developing stem cell-derived therapies for Type 1 diabetes.

Where are CRISPR Therapeutics' R&D operations based?

The company's R&D operations are based in Cambridge, Massachusetts.

How has CRISPR Therapeutics impacted the field of medicine?

CRISPR Therapeutics is at the forefront of the gene editing revolution, developing innovative therapies for serious diseases and collaborating with leading companies.

Where can I find more information about CRISPR Therapeutics?

More information about CRISPR Therapeutics can be found on their website at www.crisprtx.com.
Crispr Therapeut

Nasdaq:CRSP

CRSP Rankings

CRSP Stock Data

3.99B
84.25M
1.8%
74.08%
23.8%
Biotechnology
Biological Products, (no Disgnostic Substances)
Link
Switzerland
ZUG