LENZ Therapeutics Announces Submission of Marketing Authorization Application to the Medicines and Healthcare products Regulatory Agency for VIZZ® for the Treatment of Presbyopia in the Un...
LENZ Therapeutics, Inc. (LENZ)
Company Research
Source: GlobeNewswire
MHRA submission follows EMA validation of the VIZZ MAA in March 2026 Sixth ex-U.S. regulatory submission for VIZZ underscores accelerating global expansion SAN DIEGO, April 20, 2026 (GLOBE NEWSWIRE) -- LENZ Therapeutics, Inc. (Nasdaq: LENZ) today announced that it has submitted a Marketing Authorization Application (MAA) to the United Kingdom’s Medicines and Healthcare products Regulatory Agency (MHRA) for the review and approval of VIZZ® (aceclidine ophthalmic solution) 1.44%, the first and only aceclidine-based eye drop for the treatment of presbyopia in adults. Since receiving U.S. Food and Drug Administration (FDA) approval in July 2025, LENZ has moved rapidly to expand global access to VIZZ, with submission of the MAA in the United Kingdom representing the sixth ex-U.S. regulatory submission for VIZZ. “As we advance in the early product launch in the United States, we continue to position VIZZ for broad international expansion which now includes a key regulatory advancement
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LENZ
News
- LENZ Therapeutics, Inc. Investigated by the Portnoy Law FirmGlobeNewswire
- LENZ Therapeutics (LENZ) had its price target lowered by HC Wainwright from $56.00 to $48.00. They now have a "buy" rating on the stock.MarketBeat
- LENZ Therapeutics: Speculative But Strong Buy [Seeking Alpha]Seeking Alpha
- The Consensus EPS Estimates For LENZ Therapeutics, Inc. (NASDAQ:LENZ) Just Fell Dramatically [Yahoo! Finance]Yahoo! Finance
- Why Lenz Therapeutics Stock Plummeted by Almost 20% This Week [Yahoo! Finance]Yahoo! Finance
LENZ
Earnings
- 3/24/26 - Miss
LENZ
Sec Filings
- 4/28/26 - Form ARS
- 4/28/26 - Form DEFA14A
- 4/28/26 - Form DEF
- LENZ's page on the SEC website