Lenz Therapeutics, INC 8-K filings

Current reports — the filing a company makes when something happens that shareholders need to know about before the next quarterly report.

NASDAQ
Lenz Therapeutics reported $5.5 million in Q2 2026 revenue, driven by VIZZ sales and license agreements, alongside the launch of a new telehealth channel.
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Lenz Therapeutics reports a director's resignation and a subsequent adjustment to the Board size and Audit Committee composition.
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LENZ Therapeutics shareholders re-elected Class II directors and ratified the appointment of Ernst & Young LLP as the company's independent auditor.
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LENZ Therapeutics announced its fourth quarter and full year 2025 financial results, highlighting a successful initial launch of VIZZ for presbyopia with $1.6 million in net product revenue.
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LENZ Therapeutics announced preliminary unaudited Q4 2025 financial results, reporting $1.6 million in VIZZ net product revenue and over 20,000 prescriptions filled.
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LENZ Therapeutics, Inc. reported an adverse event of a retinal tear in a patient using VIZZ, noting pre-existing risk factors and an uncertain causal link.
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LENZ Therapeutics announced its third quarter 2025 financial results, highlighting the successful commercial launch of VIZZ for presbyopia and a strong cash position.
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LENZ Therapeutics, Inc. announced the sale of 1,748,634 shares of common stock to a single investor, generating approximately $80 million in gross proceeds.
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LENZ Therapeutics announces the commercial availability of VIZZ, the first and only FDA-approved aceclidine-based eye drop for presbyopia, in the United States.
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LENZ Therapeutics announced the US Food and Drug Administration (FDA) approved VIZZ (aceclidine ophthalmic solution) 1.44%, the first and only aceclidine-based eye drop for the treatment of presbyopia in adults.
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LENZ Therapeutics announced its second quarter 2025 financial results, highlighting the LNZ100 NDA remains on track for an August 8, 2025 PDUFA date and significant progress in global commercialization efforts.
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LENZ Therapeutics, Inc. announced the successful election of Class III and Class I directors and the ratification of Ernst & Young LLP as its independent registered public accounting firm at its 2025 annual meeting of stockholders.
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LENZ Therapeutics announces its Q1 2025 financial results, highlighting progress on its NDA for LNZ100 and a strong cash position.
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Lenz Therapeutics reports approximately $194 million in cash, cash equivalents, and marketable securities as of March 31, 2025, in anticipation of the potential approval and launch of LNZ100.
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LENZ Therapeutics has entered into a sales agreement with TD Cowen to sell up to $150 million of its common stock through an at-the-market offering program.
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LENZ Therapeutics reports financial results for 2024 and highlights progress towards the potential approval and launch of LNZ100 for presbyopia, with a PDUFA target action date of August 8, 2025.
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LENZ Therapeutics reported positive Phase 3 results for their presbyopia treatment, LNZ100, and announced the FDA's acceptance of their New Drug Application with a target action date of August 8, 2025.
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LENZ Therapeutics and Corxel Pharmaceuticals reported successful topline results from a Phase 3 trial in China for their LNZ100 eye drop, showing significant improvement in near vision for patients with presbyopia.
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LENZ Therapeutics has submitted a New Drug Application to the FDA for its LNZ100 eye drop for presbyopia, following positive Phase 3 trial results and a $30 million private placement.
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LENZ Therapeutics has submitted a New Drug Application to the U.S. Food and Drug Administration for its LNZ100 eye drop, aimed at treating presbyopia.
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LENZ Therapeutics has entered into a stock purchase agreement with Ridgeback Capital Investments for a $30 million private placement to support the development and commercialization of its presbyopia treatment, LNZ100.
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LENZ Therapeutics reported positive topline data from its Phase 3 CLARITY study for presbyopia, selected LNZ100 as its lead candidate, and anticipates a New Drug Application submission in mid-2024.
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LENZ Therapeutics' LNZ100 eye drop demonstrated strong efficacy and safety in Phase 3 trials for presbyopia, with a New Drug Application submission planned for mid-2024.
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LENZ Therapeutics has finalized its merger with Graphite Bio, debuting on Nasdaq under the ticker symbol LENZ, and is advancing its late-stage clinical assets for the treatment of presbyopia.
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Graphite Bio will enact a 1-for-7 reverse stock split and change its name to Lenz Therapeutics on March 21, 2024, in preparation for its merger with Lenz Therapeutics.
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Graphite Bio stockholders have approved the merger with LENZ Therapeutics, along with related proposals including a reverse stock split and a name change to LENZ Therapeutics, Inc.
NASDAQ
Graphite Bio has declared a special cash dividend of approximately $1.03 per share for its stockholders, contingent on the closing of its merger with Lenz Therapeutics.
NASDAQ
Graphite Bio provides supplemental disclosures to its proxy statement/prospectus in response to litigation and demand letters related to its merger with Lenz Therapeutics.