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Share Name | Share Symbol | Market | Type |
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Charles River Laboratories International Inc | NYSE:CRL | NYSE | Common Stock |
Price Change | % Change | Share Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|
0.00 | 0.00% | 209.47 | 0 | 01:00:00 |
Supporting scale-up for early-phase AAV- and LVV-based gene and gene-modified cell therapy researchers and developers
Charles River Laboratories International, Inc. (NYSE: CRL) today announced the launch of its reference materials for adeno associated virus (AAV) and lentiviral vector (LVV) portfolio, designed to streamline Cell and Gene Therapy (CGT) research and development as it scales to Good Manufacturing Practice- (GMP) quality.
Moving towards a gold standard for reference materials, Charles River is introducing six AAV reference material serotypes, offering superior empty and full capsid ratios and high vector genome concentration (GC/mL), plus five LVV reference material products, available with different combinations of promoters and reporter genes. The additional reference materials add to the Company’s extensive portfolio of plasmid and viral vector contract development and manufacturing organization (CDMO) offerings, reinforcing its concept-to-cure commitment to CGT researchers and developers by enabling partners to navigate the path from early discovery to commercial.
ASGCT Launch Charles River will officially launch its AAV and LVV reference materials with supporting case study data during the American Society of Gene and Cell Therapy (ASGCT) Annual Meeting, May 7 – 11, 2024, in Baltimore, MD.
Meet the Charles River team at Booth #327 to discuss how to streamline the CGT research and development process, and explore various presentations and scientific posters from subject matter experts, including:
To view the full list and to schedule a meeting, visit criver.com.
Cell and Gene Therapy CDMO Solutions With a strong track record supporting multiple client programs, Charles River’s viral vector CDMO center of excellence in Rockville, MD, offers integrated solutions to support CGT programs from pre-clinical research to commercial scale.
To learn more about Charles River’s CGT portfolio and gain real-world insights from a development, manufacturing, and testing perspective, join an expert roundtable webinar hosted by Human Gene Therapy, Streamlining Cell and Gene Therapy Scalability: Progress Towards a Gold Standard, moderated by James Cody, PhD, Associate Director, Technical Evaluations on May 13, 2024.
To learn more about optimizing the development of gene therapy products, join the upcoming Charles River webinar, The Roadmap to Fast-Tracking Gene Therapy Development, on June 4, 2024. The multi-disciplinary panel will explore in vitro approaches to optimize and support the development of gene therapy products, including key considerations and real-world data highlighting routes to de-risk your therapeutic product.
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About Charles River Charles River provides essential products and services to help pharmaceutical and biotechnology companies, government agencies and leading academic institutions around the globe accelerate their research and drug development efforts. Our dedicated employees are focused on providing clients with exactly what they need to improve and expedite the discovery, early-stage development and safe manufacture of new therapies for the patients who need them. To learn more about our unique portfolio and breadth of services, visit www.criver.com.
View source version on businesswire.com: https://www.businesswire.com/news/home/20240502084745/en/
Investor Contact: Todd Spencer Corporate Vice President, Investor Relations 781.222.6455 todd.spencer@crl.com
Media Contact: Amy Cianciaruso Corporate Vice President, Chief Communications Officer 781.222.6168 amy.cianciaruso@crl.com
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