Y-mAbs to Present at the 43rd Annual J.P. Morgan Healthcare Conference

YMAB 12.23.2024

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Drug:naxitamab-gqgk DANYELZA® (naxitamab-gqgk)
Diseases:high-risk neuroblastoma
Date of Upcoming Event:2025-01-15
Name of Upcoming Event:43rd Annual J.P. Morgan Healthcare Conference
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  • 01.16.2025 - 43rd Annual J.P. Morgan Healthcare Conference
  • 01.10.2025 - Y-mAbs Provides Strategic Business Update and 2025 Priorities
  • 01.10.2025 - Correcting & Replacing – Y-mAbs Provides Strategic Business Update and 2025 Priorities

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  • 01.22.2025 - 4 Statement of changes in beneficial ownership of securities
  • 01.17.2025 - 3 Initial statement of beneficial ownership of securities
  • 01.13.2025 - 8-K Current report
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NEW YORK,Dec. 23, 2024(GLOBE NEWSWIRE) --Y-mAbs Therapeutics, Inc.(the “Company” or “Y-mAbs”) (Nasdaq: YMAB), a commercial-stage biopharmaceutical company focused on the development and commercialization of novel radioimmunotherapy and antibody-based therapeutic products for the treatment of cancer, today announced thatMichael Rossi, President and Chief Executive Officer, will present at the 43rdAnnualJ.P. Morgan Healthcare ConferenceinSan Francisco, CAonWednesday, January 15, 2025at5:15 p.m. PT.

A live webcast will be available under the Events section of the Company’s investor relations website atir.ymabs.com. The webcast will be archived and available for replay for 30 days after the event.

About Y-mAbsY-mAbs is a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, radioimmunotherapy and antibody-based therapeutic cancer products. The Company’s technologies include its investigational Self-Assembly DisAssembly (“SADA”) Pretargeted Radioimmunotherapy Platform (“PRIT”) and bispecific antibodies generated using the Y-BiClone platform. The Company’s broad and advanced product pipeline includes the anti-GD2 therapy DANYELZA® (naxitamab-gqgk), the first FDA-approved treatment for patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow after a partial response, minor response, or stable disease to prior therapy.

Forward-Looking StatementsStatements in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements include, but are not limited to, statements about our business model, including financial outlook for 2024 and beyond.Words such as ‘‘anticipate,’’ ‘‘believe,’’ “contemplate,” ‘‘continue,’’ ‘‘could,’’ ‘‘estimate,’’ ‘‘expect,’’ “hope,” ‘‘intend,’’ ‘‘may,’’ ‘‘might,’’ ‘‘plan,’’ ‘‘potential,’’ ‘‘predict,’’ ‘‘project,’’ ‘‘should,’’ ‘‘target,’’ “will,” ‘‘would’,’ “guidance,” “goal,” “objective,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. The Company’s business is subject to risks and uncertainties affecting the Company including those described in the “Risk Factors” section included in the Company’s Annual Report on Form 10-K for the fiscal year endedDecember 31, 2023, and the Company’s Quarterly Report on Form 10-Q for the quarterly periods endedMarch 31, 2024, andSeptember 30, 2024, and future filings and reports by the Company. Any forward-looking statements contained in this press release speak only as of the date hereof, and the Company undertakes no obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.

SADA®, SADA PRIT®, DANYELZA® and Y-mAbs® are registered trademarks ofY-mAbs Therapeutics, Inc.

Investor Contact:Courtney DuganVP, Head of Investor Relations[email protected]

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Source: Y-mAbs Therapeutics, Inc.

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