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

Key Takeaway: CRISPR Therapeutics will present at the Morgan Stanley 24th Annual Global Healthcare Conference on September 14, 2026. The presentation will feature members of the senior management team and will be available via live webcast. The company is recognized for its advancements in gene-based therapies, including the approval of CASGEVY® for sickle cell disease.

Market Sentiment Analysis

POSITIVE FACTORS

  • CRISPR Therapeutics is presenting at a significant healthcare conference.
  • The company has a strong pipeline in gene-based medicines.
  • CASGEVY® is the first CRISPR-based therapy approved for serious diseases.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+60%
120-day peak, hindsight
Typical move
2.4%
average across 2 past catalysts
Cash runway
~84 mo
Minimal dilution risk
Lead asset
CTX112
Phase 1 · Warm Autoimmune Hemolytic Anemia (WAIHA)

Full Press Release Details

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 ir@crisprtx.com

Media Contact: +1-617-315-4493 media@crisprtx.com

Frequently Asked Questions

When is CRISPR Therapeutics presenting?

CRISPR Therapeutics will present on September 14, 2026.

Where can I watch the presentation?

The presentation will be available via live webcast on the company's website.

What is CASGEVY®?

CASGEVY® is the first CRISPR-based therapy approved for sickle cell disease.

What is the focus of CRISPR Therapeutics?

The company focuses on developing gene-based medicines for serious diseases.

Last updated: Sep 8, 2026