Press Releases September 8, 2026 08:30 AM

CRISPR Therapeutics to Present at the Morgan Stanley 24th Annual Global Healthcare Conference

CRISPR Therapeutics to Present at Morgan Stanley’s Prestigious Global Healthcare Conference Amid Pioneering Gene Therapy Advances

By Hana Yamamoto
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CRISPR Therapeutics, a leader in gene-editing based biopharmaceuticals, announced a scheduled presentation at the Morgan Stanley 24th Annual Global Healthcare Conference. The company recently marked a historic milestone with the approval of CASGEVY®, the world's first CRISPR-based therapy, and continues to advance a robust pipeline across multiple disease areas, while expanding its gene-editing technology.

CRISPR Therapeutics to Present at the Morgan Stanley 24th Annual Global Healthcare Conference
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Key Points

  • CRISPR Therapeutics will present at a major healthcare investor conference, signaling confidence in its advancements and strategic position.
  • The company achieved regulatory approval for CASGEVY®, the first CRISPR-based therapy targeting sickle cell disease and beta thalassemia, underscoring its leadership in gene-editing therapeutics.
  • CRISPR Therapeutics’ diversified pipeline spans hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine, and rare diseases, supported by proprietary SyNTase™ editing platform and collaborations with firms like Vertex Pharmaceuticals.

ZUG, Switzerland and BOSTON, Sept. 08, 2026 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP) today announced that members of its senior management team will present at the Morgan Stanley 24th Annual Global Healthcare Conference on Monday, September 14, 2026 at 1:05 p.m. EST.

A live webcast of the fireside chat 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 the presentation.

About CRISPR Therapeutics
CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. Founded over a decade ago as an early pioneer in CRISPR/Cas9 gene editing, the Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world’s first CRISPR-based therapy, for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. Today, CRISPR Therapeutics is advancing a broad, diversified pipeline spanning hemoglobinopathies, cardiovascular disease, autoimmune disease, oncology, regenerative medicine and rare diseases. The Company is also expanding its gene editing toolkit through SyNTase™ editing, its novel, proprietary platform designed to enable precise, efficient, and scalable gene correction. To accelerate its impact, CRISPR Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. To learn more, visit www.crisprtx.com.

Investor Contact:
+1-617-307-7503
[email protected] 

Media Contact:
+1-617-315-4493
[email protected]


Risks

  • Gene therapy and CRISPR-based technology remain emerging fields with inherent scientific, clinical, and regulatory uncertainties that could impact approvals, market adoption, and commercial success.
  • Competition from other biopharmaceutical companies in gene editing and alternative medical fields could affect CRISPR Therapeutics’ growth and market share.
  • Market volatility and investor sentiment in the biotech and healthcare sectors may affect stock price despite positive clinical and corporate developments.

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