CRISPR Therapeutics to Participate in the Chardan’s 5th Annual Genetic Medicines Conference
CRISPR Therapeutics announced participation in Chardan’s 5th Annual Genetic Medicines Conference on October 4, 2021, at 2:00 p.m. ET.
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CRISPR Therapeutics announced participation in Chardan’s 5th Annual Genetic Medicines Conference on October 4, 2021, at 2:00 p.m. ET. Senior management will present insights on their innovative gene-based medicines targeting serious diseases. A live webcast will be accessible via the Company's website, with a replay available for 14 days post-event. The company is noted for its leading gene editing technology, CRISPR/Cas9, and has collaborations with Bayer and Vertex Pharmaceuticals.
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ZUG, Switzerland and CAMBRIDGE, Mass., Sept. 28, 2021 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, today announced that members of its senior management team are scheduled to participate in the Chardan’s 5th Annual Genetic Medicines Conference on Monday, October 4, 2021 at 2:00 p.m. ET.
A live webcast of the event will be available on the "Events & Presentations" page in the Investors section of the Company's website at https://crisprtx.gcs-web.com/events. A replay of the webcast will be archived on the Company's website for 14 days following each presentation.
About CRISPR Therapeutics
CRISPR Therapeutics is a leading gene editing company focused on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. CRISPR/Cas9 is a revolutionary gene editing technology that allows for precise, directed changes to genomic DNA. CRISPR Therapeutics has established a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine and rare diseases. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic collaborations with leading companies including Bayer, Vertex Pharmaceuticals and ViaCyte, Inc. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Cambridge, Massachusetts, and business offices in San Francisco, California and London, United Kingdom. For more information, please visit www.crisprtx.com.
CRISPR THERAPEUTICS® word mark and design logo are trademarks and registered trademarks of CRISPR Therapeutics AG. All other trademarks and registered trademarks are the property of their respective owners.
Investor Contact:
Susan Kim
+1-617-307-7503
susan.kim@crisprtx.com
Media Contact:
Rachel Eides
+1-617-315-4493
rachel.eides@crisprtx.com
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