Artiva Biotherapeutics Pauses Phase 3 Trial Following Patient Death
Artiva Biotherapeutics has paused enrollment and dosing in its Phase 3 clinical trial at the request of the FDA following a patient death.
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Artiva Biotherapeutics Plunges Into Crisis Over Patient Deaths and Possible Liquidation
Artiva Biotherapeutics ends its AlloNK program after fatal safety events, slashes 94% of its workforce, and weighs strategic liquidation.
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Artiva Biotherapeutics Announces Workforce Reduction and Strategic Alternatives Review
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Artiva Biotherapeutics Discontinues Development of Lead Candidate AlloNK and Initiates Strategic Review
Artiva Biotherapeutics has decided to halt the development of its lead product candidate, AlloNK, and is exploring strategic alternatives to maximize stockholder value.
8-K filing — Artiva Biotherapeutics, Inc. (ARTV)
Filed: 2026-10-27 AccNo: 0001193125-26-432806 Size: 178 KB Item 2.02: Results of Operations and Financial Condition Item 2.05: Cost Associated with Exit or Disposal Activities Item 9.01: Financial Statements and Exhibits