Press Releases May 6, 2026 08:30 AM

CRISPR Therapeutics to Present at the Bank of America Securities 2026 Global Healthcare Conference

CRISPR Therapeutics to Present at Bank of America Securities 2026 Global Healthcare Conference

By Maya Rios CRSP

CRISPR Therapeutics announces its senior management team will present at the upcoming Bank of America Securities 2026 Global Healthcare Conference, highlighting its pioneering gene editing therapies and robust pipeline. The company recently received approval for CASGEVY4, the first CRISPR-based therapy for certain serious blood diseases, and is advancing diverse therapeutic areas while expanding its gene editing platforms and strategic collaborations.

CRISPR Therapeutics to Present at the Bank of America Securities 2026 Global Healthcare Conference
CRSP

Key Points

  • CRISPR Therapeutics will present at a major global healthcare conference, increasing investor visibility.
  • The company achieved a major milestone with FDA approval of CASGEVY4, the first CRISPR-based therapy for sickle cell disease and beta thalassemia.
  • CRISPR is expanding its pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine, and rare diseases and developing novel gene editing technologies like SyNTase3.
  • The company's strategic partnerships with leading biopharma firms, including Vertex Pharmaceuticals, support its growth and innovation.

ZUG, Switzerland and BOSTON, May 06, 2026 (GLOBE NEWSWIRE) -- CRISPR Therapeutics (Nasdaq: CRSP) today announced that members of its senior management team will present at the Bank of America Securities 2026 Global Healthcare Conference on Tuesday, May 12, 2026 1:40 p.m. PDT.

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

  • Therapeutic developments in gene editing face scientific and regulatory uncertainties that could delay or limit product approvals.
  • The competitive landscape in gene editing and biopharma may impact CRISPR Therapeutics' market share and partnerships.
  • Market adoption and reimbursement for novel gene therapies like CASGEVY4 may present access and commercial challenges.

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