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 (CRSP) is a clinical-stage biopharmaceutical leader pioneering CRISPR/Cas9 gene editing therapies for serious diseases. This page aggregates official announcements, clinical trial updates, and strategic developments directly from the company and verified sources.
Investors and researchers will find timely updates on therapeutic programs targeting hemoglobinopathies, oncology, and autoimmune disorders. Track regulatory milestones, partnership announcements with industry leaders, and financial performance reports. All content is curated to meet investor needs for decision-making clarity.
Key updates include progress in allogeneic CAR-T cell therapies, hemoglobinopathy treatment approvals, and manufacturing scale-up initiatives. Bookmark this page for structured access to CRISPR Therapeutics' latest scientific advancements and business developments.
CRISPR Therapeutics (Nasdaq: CRSP) has announced participation in the 22nd Annual Needham Healthcare Conference, taking place virtually from April 17-20, 2023. The company's CEO, Sam Kulkarni, will present during a fireside chat on April 19, 2023, at 3:00 p.m. ET. The session will be accessible via a live webcast on the company's Investors page, and will be available for replay for 14 days post-event. CRISPR Therapeutics is recognized for its innovative approach in gene editing, leveraging the CRISPR/Cas9 technology to develop treatments for various serious diseases, including hemoglobinopathies, oncology, and rare diseases, in collaboration with partners like Bayer and Vertex Pharmaceuticals.
Vertex Pharmaceuticals and CRISPR Therapeutics have completed the rolling Biologics License Applications (BLAs) for the investigational treatment exagamglogene autotemcel (exa-cel) aimed at sickle cell disease (SCD) and transfusion-dependent beta thalassemia (TDT). The applications, submitted to the FDA, include requests for Priority Review, potentially expediting the review period to eight months. The filings are supported by ongoing Phase 3 clinical studies and previous data presented at the ASH Annual Meeting in December 2022. Both companies highlight their commitment to the advancement of CRISPR technology in treating genetic diseases.
CRISPR Therapeutics (Nasdaq: CRSP) announced the resignation of Brad Bolzon, Ph.D., from its Board of Directors after nearly ten years. Bolzon's contributions were pivotal in shaping the company's vision and strategy, with management acknowledging his strategic insights in advancing gene editing technology. The company focuses on developing transformative gene-based medicines using its proprietary CRISPR/Cas9 platform, targeting serious diseases across multiple therapeutic areas. CRISPR Therapeutics has established strategic partnerships with leading firms such as Bayer and Vertex Pharmaceuticals.
Vertex Pharmaceuticals has secured a non-exclusive licensing agreement with CRISPR Therapeutics for its CRISPR/Cas9 technology, aiming to enhance the development of hypoimmune cell therapies for Type 1 Diabetes (T1D). Vertex will pay
CRISPR Therapeutics (Nasdaq: CRSP) announced the presentation of preclinical data at the AACR 2023 Annual Meeting in Orlando, FL, scheduled for April 14-19, 2023. The presentation titled CTX112 and CTX131: Next-generation CRISPR/Cas9-engineered allogeneic CAR T cells highlights novel edits that enhance potency and efficacy for treating lymphoid and solid tumors.
This session will take place on April 16, 2023, from 1:25 to 1:40 p.m. ET at the Tangerine Ballroom 2. Data will be under embargo until the session starts, with a copy of the presentation available post-session on their official website.