Press Releases April 6, 2026 08:00 PM

Lyell Immunopharma Announces Participation in 25th Annual Needham Virtual Healthcare Conference

Lyell Immunopharma to Present at 25th Annual Needham Virtual Healthcare Conference

By Nina Shah LYEL
Lyell Immunopharma Announces Participation in 25th Annual Needham Virtual Healthcare Conference
LYEL

Lyell Immunopharma, a late-stage clinical company focused on next-generation CAR T-cell therapies for cancer, announced its participation in the 25th Annual Needham Virtual Healthcare Conference. Senior management will present on April 14, 2026, highlighting the company's pipeline and manufacturing capabilities for potential commercial launch.

Key Points

  • Lyell is advancing next-generation CAR T-cell therapies targeting hematologic malignancies and solid tumors.
  • Management will present at a prominent healthcare investor conference, providing updates on clinical development and manufacturing capacity.
  • Lyell's LyFE Manufacturing Center has capability to produce over 1,200 CAR T-cell doses at full capacity, supporting potential commercial launches.

SOUTH SAN FRANCISCO, Calif., April 07, 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 present and participate in the 25th Annual Needham Virtual Healthcare Conference on Tuesday, April 14, 2026, at 11:00 am Eastern Time.

A live webcast of the presentation 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 presentation date.

About Lyell

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 LyFE Manufacturing Center™ has commercial launch capability and can manufacture more than 1,200 CAR T-cell doses at full capacity. 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 presentation and 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 Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on March 12, 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:

Pablo Fenton
Associate Director, Investor Relations and Corporate Communications
[email protected]


Risks

  • Dependence on successful clinical outcomes to realize therapeutic potential, inherent to late-stage biotech companies.
  • Risks related to manufacturing scale-up and ability to supply drug in commercial quantities.
  • Uncertainties associated with forward-looking statements including timelines and performance, subject to various business and regulatory risks.

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