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LENZ Therapeutics Announces Everest Medicines Acquired Rights to Develop and Commercialize VIZZ® (LNZ100) in Greater China

(Very Positive)

LENZ Therapeutics (Nasdaq: LENZ) announced that Everest Medicines acquired rights to develop, manufacture and commercialize VIZZ (LNZ100) for presbyopia in Greater China.

LENZ may receive up to $85 million in remaining milestones, additional payments, and tiered mid single-digit to low double-digit royalties on net sales.

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Positive

  • Everest Medicines acquires rights to develop and commercialize VIZZ (LNZ100) in Greater China
  • LENZ eligible for up to $85 million in remaining regulatory and sales milestones
  • LENZ to receive tiered mid single-digit to low double-digit royalties on Greater China net sales
  • Additional payments possible to LENZ tied to the CORXEL–Everest agreement execution
  • NDA for LNZ100 submitted in China in September 2025 with approval anticipated in Q1 2027
  • Product already approved in the United States and under regulatory review in China

Negative

  • None.

News Market Reaction – LENZ

-4.14%
-4.14% Session close to close

In the Jun 8 session, LENZ declined 4.14%, reflecting a moderate negative market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement reinforces LENZ’s ex-U.S. partnership strategy by assigning VIZZ rights in Greater...
Analysis

This announcement reinforces LENZ’s ex-U.S. partnership strategy by assigning VIZZ rights in Greater China to Everest Medicines, with up to $85.0 million in remaining milestones plus royalties. It complements prior regulatory filings, including the UK MAA, while the NDA in China, submitted in September 2025, targets anticipated approval in Q1 2027. Investors may watch execution on commercialization, regulatory timelines, and future milestone realization.

Key Figures

VIZZ concentration: 1.44% China NDA submission date: September 2025 China approval timing: Q1 2027 +2 more
5 metrics
VIZZ concentration 1.44% Aceclidine ophthalmic solution strength for presbyopia
China NDA submission date September 2025 NDA for LNZ100 submitted to China CDE/NMPA
China approval timing Q1 2027 Approval for LNZ100 in China anticipated
Milestone potential $85.0 million Remaining regulatory and sales milestones from Greater China deal
Regions covered 4 regions Chinese mainland, Hong Kong SAR, Macao SAR, Taiwan region

Historical Context

5 past events · Latest: May 26 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 26 Investor conferences Positive +2.6% Announcement of participation in three upcoming investor conferences.
May 11 Q1 2026 earnings Negative -20.8% First commercial quarter with low revenue and a widened net loss.
May 04 Earnings date & conferences Neutral +4.5% Scheduled Q1 2026 results webcast and conference attendance details.
Apr 20 UK MAA submission Positive -0.5% Marketing Authorization Application for VIZZ submitted to UK MHRA.
Mar 24 FY 2025 earnings Positive -17.9% Q4/FY 2025 results with commercial launch progress and ex-U.S. deals.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings and progress updates have sometimes seen sharp negative reactions, while regulatory milestones have not always been rewarded, indicating a tendency for selling into news.

Recent Company History

Over the last few months, LENZ advanced VIZZ with multiple ex-U.S. regulatory submissions, including a UK MAA on Apr 20, 2026, following FDA approval and EMA validation. Commercialization began in late 2025, with Q1 2026 revenue of $1.9M but a wider net loss and notable post-earnings selloffs of -17.91% and -20.82%. Today’s Greater China rights transfer to Everest extends this ex-U.S. partnership strategy while the stock trades near its $6.61 52-week low.

Key Terms

new drug application, nda, center for drug evaluation, national medical products administration, +4 more
8 terms
new drug application regulatory
"The New Drug Application (NDA) for LNZ100 in China was submitted..."
A new drug application is a formal request submitted to government regulators seeking approval to market a new medicine. It is like a detailed proposal that shows the drug has been tested for safety and effectiveness. For investors, receiving approval signals that the drug may soon become available for sale, potentially leading to revenue growth and impacting the company's value.
nda regulatory
"The New Drug Application (NDA) for LNZ100 in China was submitted..."
An NDA, or nondisclosure agreement, is a legal contract that keeps certain information private between parties. It’s like a promise not to share sensitive details, helping protect business ideas, strategies, or data from being leaked or used without permission. For investors, NDAs help ensure that confidential information remains secure, enabling trust and open communication during business discussions.
center for drug evaluation regulatory
"submitted to the Center for Drug Evaluation (CDE) of the National..."
A center for drug evaluation is the government agency division that reviews safety, effectiveness and quality data for new medicines and applications to sell them. Think of it as a gatekeeper that checks scientific evidence and decides whether a drug can reach patients; its decisions shape how quickly a drug can be approved, marketed or withdrawn, so investors watch its rulings as major milestones that affect a company’s sales prospects and regulatory risk.
national medical products administration regulatory
"Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA)..."
The National Medical Products Administration is the government agency responsible for reviewing, approving and supervising drugs, vaccines, medical devices and related products. Think of it as the country’s gatekeeper for medical products: its decisions determine whether a product can be sold, how quickly it reaches patients and what safety or labeling requirements apply, so its rulings directly affect a company’s sales prospects, regulatory risk and investor valuation.
nmpa regulatory
"Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA)..."
China’s National Medical Products Administration is the government agency that reviews and approves medicines, medical devices and cosmetics, and enforces safety and quality rules. Think of it as a gatekeeper or traffic controller: its approvals and inspections determine whether a product can be sold, how quickly it reaches patients, and what safety or labeling rules apply—factors that directly affect a healthcare company’s sales, costs and regulatory risk for investors.
asset purchase agreement financial
"entered into an Asset Purchase Agreement with Corxel Pharmaceuticals..."
An asset purchase agreement is a legal contract in which a buyer agrees to buy specific assets and contracts of a business rather than buying the company’s stock or ownership. It matters to investors because it determines exactly what is being bought and what liabilities stay behind — like buying the furniture and equipment from a store but not the building or past debts — which affects the deal’s value, taxes and future risk exposure.
presbyopia medical
"eye drop for the treatment of presbyopia, today announced that Everest..."
Presbyopia is the gradual loss of the eye’s ability to focus on close objects as the lens stiffens with age, causing tasks like reading or using a phone to require holding things farther away or using glasses. It matters to investors because it drives steady demand for corrective products and treatments—such as reading glasses, contact lenses, surgical procedures and emerging drugs—much like an aging population consistently needs new or replacement consumer goods and services.
ophthalmology medical
"therapeutic areas of focus including ophthalmology, CKM (cardiovascular..."
Ophthalmology is the branch of medicine that diagnoses, treats and prevents eye diseases and vision problems, ranging from routine exams to surgery. For investors, it matters because advances, approvals or setbacks in eye drugs, surgical tools, diagnostics or implants can change sales, regulatory risk and long-term demand—think of it as the medical ‘repair and upgrade’ market for a vital organ.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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The New Drug Application for LNZ100 in China was submitted September 2025 with approval anticipated in Q1 2027

SAN DIEGO, June 07, 2026 (GLOBE NEWSWIRE) -- LENZ Therapeutics, Inc. (Nasdaq: LENZ, “LENZ” or the “Company”), a pharmaceutical company focused on the commercialization of VIZZ® (aceclidine ophthalmic solution) 1.44%, the first and only aceclidine-based eye drop for the treatment of presbyopia, today announced that Everest Medicines (HKEX1952, or “Everest”), has entered into an Asset Purchase Agreement with Corxel Pharmaceuticals (“CORXEL”) to acquire the rights to develop, manufacture, and commercialize VIZZ (LNZ100) in Greater China, including Chinese mainland, Hong Kong SAR, Macao SAR, and Taiwan region.

Everest Medicines is a biopharmaceutical company focused on discovering, developing, manufacturing and commercializing innovative pharmaceutical products that address critical unmet medical needs for patients in global markets, with therapeutic areas of focus including ophthalmology, CKM (cardiovascular, kidney, and metabolic), autoimmune and critical care.

The New Drug Application (NDA) for LNZ100 in China was submitted to the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) of the People’s Republic of China (PRC) in September 2025, with approval anticipated in Q1 2027. As part of this agreement, Everest will be assigned and transferred the rights and obligations under the LENZ License Agreement entered into by CORXEL in April 2022 and certain related ancillary agreements. LENZ is eligible to receive up to $85.0 million in remaining regulatory and sales milestones, as well as tiered mid single-digit to low double-digit royalties on net sales in Greater China. LENZ is also now eligible to receive additional payments in connection with the execution of the agreement between CORXEL and Everest.

"The acquisition of LNZ100 represents an important step in advancing Everest’s strategic focus in ophthalmology. LNZ100 is a differentiated asset with meaningful clinical value and strong commercial potential in the treatment of presbyopia,” said Yifang Wu, Chairman of the Board of Everest Medicines. “As the presbyopia patient population continues to grow, significant unmet needs remain in non-invasive treatment options. We believe LNZ100 has the potential to offer patients a novel, non-invasive therapeutic option and to further broaden the landscape of innovative ophthalmic treatments. The product has already been approved in the United States and is currently under regulatory review in China. We will continue to advance its development and commercialization to make this therapy accessible to presbyopia patients."

“We thank the CORXEL team for their partnership in the clinical execution and regulatory stewardship of LNZ100 in China”, said Eef Schimmelpennink, President and Chief Executive Officer of LENZ Therapeutics. “We look forward to collaborating with Everest as we approach regulatory approval and commercial launch in China, providing a transformative new treatment option for millions of adults living with presbyopia.”

About LENZ Therapeutics

LENZ Therapeutics is a pharmaceutical company focused on the commercialization of VIZZ® (aceclidine ophthalmic solution) 1.44%, the first and only FDA-approved aceclidine-based eye drop for the treatment of presbyopia, a condition impacting an estimated 1.8 billion people globally and 128 million people in the United States. LENZ is commercializing VIZZ in the United States and continues to establish licensing partnerships internationally to provide access to VIZZ globally. LENZ is headquartered in San Diego, California. For more information, visit www.VIZZ.com and www.lenz-tx.com.

About Everest Medicines

Everest Medicines is a biopharmaceutical company focused on discovering, developing, manufacturing and commercializing innovative pharmaceutical products that address critical unmet medical needs for patients in global markets. The management team of Everest Medicines has deep expertise and an extensive track record both in China and with leading global pharmaceutical companies. The Company’s therapeutic areas of focus include CKM (cardiovascular, kidney, and metabolic), autoimmune, ophthalmology and critical care. Everest Medicines has developed a fully integrated commercialization platform that combines omnichannel commercial capabilities with end-to-end product lifecycle management. Leveraging its proprietary mRNA platform, the Company is advancing its existing pipeline, including mRNA in vivo CAR-T and mRNA cancer vaccines, while selectively expanding into additional high-value therapeutic areas with blockbuster potential, and accelerating its global expansion. For more information, please visit the Company’s website: www.everestmedicines.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of United States federal securities laws. You can identify forward-looking statements by words such as “may,” “will,” “could,” “can,” “would,” “should,” “expect,” “intend,” “plan,” “anticipate,” “believe,” “estimate,” “predict,” “project,” “potential,” “poised,” “continue,” “ongoing” or the negative of these terms or other comparable terminology, but not all forward-looking statements will contain these words. Forward-looking statements in this press release include, but are not limited to, statements regarding the potential of approval of LNZ100 in Greater China; and plans and expectations regarding the commercialization of LNZ100 in China, if approved. These statements are based on numerous assumptions concerning LENZ, VIZZ, target markets and regulatory agencies and involve substantial risks, uncertainties and other factors that could cause actual results to differ materially from those projected, expressed or implied by these forward-looking statements, including risks related to regulatory approvals, market conditions, and those risk factors described in the section titled “Risk Factors” in our Quarterly Report on Form 10-Q filed for the quarter ended March 31, 2026 and our subsequent filings with the Securities and Exchange Commission. We cannot assure you that the forward-looking statements in this press release or the assumptions upon which they are based will prove to be accurate. The forward-looking statements in this press release are made as of the date of this press release. Except as otherwise required by applicable law, LENZ disclaims any duty to update any forward-looking statements. You should, therefore, not rely on these forward-looking statements as representing our views as of any date subsequent to the date of this press release.

Contact:
Dan Chevallard
LENZ Therapeutics
IR@LENZ-tx.com


FAQ

What did LENZ (NASDAQ: LENZ) announce about VIZZ (LNZ100) in Greater China on June 7, 2026?

LENZ announced that Everest Medicines acquired rights to develop, manufacture and commercialize VIZZ (LNZ100) for presbyopia in Greater China. According to LENZ, Everest will assume the LENZ license and related agreements previously held by Corxel, covering mainland China, Hong Kong, Macao and Taiwan.

How much milestone and royalty revenue could LENZ earn from VIZZ (LNZ100) in Greater China?

LENZ could earn up to $85 million in remaining regulatory and sales milestones from VIZZ (LNZ100) in Greater China. According to LENZ, the company is also entitled to tiered mid single-digit to low double-digit royalties on net sales, plus additional payments linked to the Everest agreement.

When was the China NDA for LNZ100 submitted and when is approval anticipated?

The New Drug Application for LNZ100 in China was submitted in September 2025, with approval anticipated in Q1 2027. According to LENZ, the filing went to the Center for Drug Evaluation of the National Medical Products Administration in the People’s Republic of China.

Who will develop and commercialize VIZZ (LNZ100) in Greater China under the new LENZ deal?

Everest Medicines will develop, manufacture and commercialize VIZZ (LNZ100) in Greater China under the new arrangement. According to LENZ, Everest is acquiring Corxel’s rights and obligations under the existing LENZ license, including territories of mainland China, Hong Kong, Macao and Taiwan.

What does the VIZZ (LNZ100) Greater China transaction mean for LENZ shareholders?

The transaction gives LENZ potential milestone payments, royalties and added upfront-related payments without direct commercialization costs in Greater China. According to LENZ, the company remains eligible for up to $85 million in milestones plus tiered royalties, offering an additional revenue stream if VIZZ sales materialize.

Is VIZZ (LNZ100) already approved and what is its status in China?

VIZZ (LNZ100) is already approved in the United States and is under regulatory review in China. According to Everest’s commentary, the product targets presbyopia and aligns with its ophthalmology strategy, with China NDA approval anticipated in the first quarter of 2027.