Press Releases September 14, 2026 07:00 AM

Lyell Immunopharma To Participate in the Baird 2026 Global Healthcare Conference

Lyell Immunopharma Announces Participation in Baird 2026 Global Healthcare Conference with Fireside Chat Webcast

By Marcus Reed
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LYEL

Lyell Immunopharma, a late-stage clinical company developing next-generation CAR T-cell therapies for cancer, will participate in the Baird 2026 Global Healthcare Conference. Senior management will discuss the company's clinical progress and manufacturing capabilities via a webcast. The company emphasizes its proprietary manufacturing center's capacity to support potential commercial launch.

Lyell Immunopharma To Participate in the Baird 2026 Global Healthcare Conference
LYEL
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Key Points

  • Lyell is advancing next-generation CAR T-cell therapies targeting hematologic malignancies and solid tumors, focusing on durable and consistent clinical responses.
  • The company will participate in a prominent healthcare conference, providing updates to investors and stakeholders.
  • Lyell's proprietary manufacturing center, LyFE Manufacturing Center™, is expected to support commercial launch with the ability to produce over 1,200 CAR T-cell doses annually.

SOUTH SAN FRANCISCO, Calif., Sept. 14, 2026 (GLOBE NEWSWIRE) -- Lyell Immunopharma, Inc. (Nasdaq: LYEL), a late-stage clinical company advancing a pipeline of next-generation chimeric antigen receptor (CAR) T-cell therapies for patients with cancer, today announced that members of its senior management team will participate in the Baird 2026 Global Healthcare Conference on Tuesday, September 15, 2026, in New York with a fireside chat scheduled for 2:00 pm Eastern Time.

A live webcast of the fireside chat can be accessed through the Investors section of the Company's website at www.lyell.com. A replay of the webcast will be available on the Company's website following the event.

About Lyell Immunopharma, Inc.

Lyell is a late-stage clinical company advancing a pipeline of next-generation CAR T-cell therapies for patients with hematologic malignancies and solid tumors. To realize the potential of cell therapy for cancer, Lyell utilizes a suite of technologies to arm CAR T cells with enhancements needed to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical responses, including the ability to resist exhaustion, maintain qualities of durable stemness and function in the hostile tumor microenvironment. Lyell’s proprietary LyFE Manufacturing Center™ has commercial launch capability and is expected to have the capacity to manufacture more than 1,200 CAR T-cell doses per year. To learn more, please visit www.lyell.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements expressed or implied in this press release include, but are not limited to, statements regarding: Lyell management’s planned participation at an investor conference; the potential clinical benefits and therapeutic potential of Lyell’s product candidates; and the sufficiency of the capacity of LyFE to manufacture drug supply through potential commercial launch. These statements are based on Lyell’s current plans, objectives, estimates, expectations and intentions, are not guarantees of future performance and inherently involve significant risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, but are not limited to, risks and uncertainties described under the heading “Risk Factors” in Lyell’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2026, filed with the Securities and Exchange Commission on August 6, 2026. Forward-looking statements contained in this press release are made as of this date, and Lyell undertakes no duty to update such information except as required under applicable law.

Contact:

Lyell Investor Relations
[email protected]


Risks

  • Clinical benefits and therapeutic potential of product candidates are not guaranteed and involve significant risks and uncertainties.
  • Manufacturing scale-up and commercial launch capacity, though planned, may face operational or regulatory challenges.
  • Forward-looking statements indicate that actual results and timing may differ materially due to market, clinical trial, and regulatory risks outlined in company filings.

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