Press Releases May 28, 2026 08:00 AM

Prime Medicine to Present at Jefferies Global Healthcare Conference

Prime Medicine CEO to Present at Jefferies Global Healthcare Conference Highlighting Gene Editing Innovation

By Priya Menon PRME

Prime Medicine announced CEO Allan Reine's participation in a fireside chat at the Jefferies Global Healthcare Conference on June 4, 2026. The presentation will focus on the company's proprietary Prime Editing platform designed to create one-time curative genetic therapies targeting liver, lung, immunology, and oncology diseases. Prime Medicine aims to expand therapeutic applications across various genetic, immunologic, cancer, and infectious diseases.

Prime Medicine to Present at Jefferies Global Healthcare Conference
PRME

Key Points

  • Prime Medicine's CEO will present at a major healthcare investor conference, increasing visibility among investors and industry stakeholders.
  • The company is advancing a versatile Prime Editing platform capable of precise gene editing with potential to address thousands of genetic mutations.
  • Current focus programs target liver, lung, immunology, and oncology diseases with plans to broaden therapeutic indications sustainably.

CAMBRIDGE, Mass., May 28, 2026 (GLOBE NEWSWIRE) -- Prime Medicine, Inc. (Nasdaq: PRME), a biotechnology company committed to delivering a new class of differentiated one-time curative genetic therapies, today announced that Allan Reine, M.D., Chief Executive Officer of Prime Medicine, will participate in a fireside chat at the Jefferies Global Healthcare Conference on Thursday, June 4, 2026, at 12:50 p.m. ET in New York, NY.

A live audio webcast of the presentation will be available under “Events & Presentations” in the News & Events section of the Company’s website at www.primemedicine.com. A replay of the webcast will be available on the Prime Medicine website for 90 days following the event.

About Prime Medicine

Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is deploying its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated one-time curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. Taken together, Prime Editing’s versatile gene editing capabilities could unlock opportunities across thousands of potential indications.

Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: liver, lung, and immunology and oncology. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. Over time, the Company intends to maximize Prime Editing’s broad and versatile therapeutic potential, as well as the modularity of the Prime Editing platform, to rapidly and efficiently expand beyond the diseases in its current pipeline, potentially including additional genetic diseases, immunological diseases, cancers, infectious diseases, and targeting genetic risk factors in common diseases, which collectively impact millions of people. For more information, please visit www.primemedicine.com.

© 2026 Prime Medicine, Inc. All rights reserved. PRIME MEDICINE, the Prime Medicine logos, and PASSIGE are trademarks of Prime Medicine, Inc. All other trademarks referred to herein are the property of their respective owners.

Investor and Media Contacts

Gregory Dearborn
Prime Medicine
857-209-0696
[email protected] 

Hannah Deresiewicz
Precision AQ
212-362-1200
[email protected]


Risks

  • Gene editing therapies face significant regulatory hurdles and clinical development risks before commercialization.
  • There is inherent uncertainty in the clinical efficacy and safety of novel gene editing approaches which may impact development timelines.
  • Market adoption and reimbursement challenges exist for innovative genetic therapies, affecting commercial success.

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