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

Key Takeaway: CRISPR Therapeutics announced that its senior management will present at the Bank of America Securities 2026 Global Healthcare Conference on May 12, 2026. The presentation will include a live webcast, which will be available on the company's website. CRISPR Therapeutics is known for its pioneering work in gene editing and has a diverse pipeline of therapies.
Price reaction · baseline $52.38 (2026-05-05 close) · hit after-hours · clean, no other CRSP news in the window
day 0 close · peak
+5.2%
day 1
+0.1%
day 3
+3.1%

Market Sentiment Analysis

POSITIVE FACTORS

  • CRISPR Therapeutics is presenting at a major healthcare conference.
  • The company has a strong pipeline in gene-based medicines.
  • They have achieved a historic milestone with the approval of the first CRISPR-based therapy.

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
CTX340
Phase 1 · Hypertension

Full Press Release Details

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 athttps://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 TherapeuticsCRISPR 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, visitwww.crisprtx.com.

Frequently Asked Questions

When will CRISPR Therapeutics present at the conference?

CRISPR Therapeutics will present on May 12, 2026, at 1:40 p.m. PDT.

Where can I watch the presentation?

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

What is CRISPR Therapeutics known for?

CRISPR Therapeutics is known for developing gene-based medicines and pioneering CRISPR/Cas9 gene editing.

What milestone has CRISPR Therapeutics achieved?

The company achieved a milestone with the approval of the world's first CRISPR-based therapy.

Last updated: May 6, 2026