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LENZ Therapeutics Reports Second Quarter 2026 Financial Results and Recent Corporate Highlights

(Very Positive)
Tags

LENZ Therapeutics (Nasdaq: LENZ) reported Q2 2026 total revenue of $5.5 million, including $1.7 million in VIZZ product sales from roughly 27,000 packs and $3.8 million in license revenue, driven by milestone and sublicense payments. VIZZ has seen strong early adoption, with over 13,000 unique prescribers since launch and more than 60% of ePharmacy patients purchasing multiple monthly packs, tracking to about five packs annually in early cohorts.

LENZ expanded its ex‑U.S. footprint with new or advanced agreements in Australia/New Zealand, Canada, Greater China and Saudi Arabia, and now has nine ex‑U.S. regulatory filings. Q2 SG&A rose to $39.4 million on launch spending, there was no R&D expense after FDA approval, and net loss widened to $31.9 million. Cash, cash equivalents and marketable securities totaled $220.0 million at June 30, 2026.

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Positive

  • Total revenue $5.5M in Q2 2026 vs $5.0M in 2025
  • VIZZ product sales $1.7M on ~27,000 packs in Q2 2026
  • High patient persistence with 60%+ ePharmacy patients buying multiple packs
  • 13,000+ unique prescribers and ~75% prescribing VIZZ multiple times
  • Strong liquidity with $220.0M in cash, equivalents and marketable securities
  • Up to $150M+ remaining milestones from Théa and Greater China arrangements

Negative

  • Net loss $31.9M in Q2 2026, $73.4M for six months
  • SG&A expenses $39.4M in Q2 and $84.3M for six months
  • License revenue $3.8M in Q2 2026 vs $5.0M in 2025
  • Cash and marketable securities declined to $220.0M from $292.3M at year-end 2025

News Explained

As a historical liquidity benchmark, LENZ Therapeutics had $24.772 million of cash and equivalents at March 31, 2026, equal to 66.4 days of that quarter’s operating cash use; this does not measure the company’s June 30 liquidity, which also included marketable securities.

Sources and calculations
  • Cash and equivalents vs quarterly operating cash outflow, in days of cash use $24,772,000 / ($33,582,000 / 90) = [object Object]

Market Context

The tag-specific record averaged -14.32% across five earnings events, adding a historically negative...
Analysis

The tag-specific record averaged -14.32% across five earnings events, adding a historically negative comparison to this report. High short positioning was a separate risk factor; subsequent monitoring would center on commercial sales and losses.

Key Figures

Total Revenue: $5.5 million Product Sales: $1.7 million Product Sales Growth: 9% +5 more
8 metrics
Total Revenue $5.5 million Q2 2026
Product Sales $1.7 million Q2 2026; approximately 27,000 packs sold
Product Sales Growth 9% Q2 2026 versus Q1 2026
Patient Refill Rate Over 60%; 5 packs per year ePharmacy patients since launch
Unique Prescribers Over 13,000 From launch through Q2 2026
Cash and Securities $220.0 million As of June 30, 2026
Net Loss $31.9 million Q2 2026
Net Loss Per Share $1.02 Q2 2026, basic and diluted

Previous Earnings Reports

5 past events · Latest: May 11 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 11 Q1 earnings report Positive -20.8% Reported quarterly revenue, commercial uptake, cash position, and net loss.
Mar 24 Q4 earnings report Positive -17.9% Reported quarterly results, commercial progress, cash, partnerships, and international regulatory filings.
Jan 07 Preliminary earnings report Positive -6.6% Reported preliminary product revenue, prescription growth, prescriber expansion, and international partnership activity.
Nov 05 Q3 earnings report Positive -23.5% Reported FDA approval, commercial launch progress, partnerships, cash, and quarterly net loss.
Jul 30 Q2 earnings report Positive -2.9% Reported regulatory progress, licensing potential, sales-force hiring, cash, and quarterly net loss.

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

Pattern Detected

All five tag-matched earnings events had negative 24-hour reactions, averaging -14.32%.

Key Terms

epharmacy, marketing authorization application, mhra, new drug submission, +1 more
5 terms
epharmacy technical
"over 60% of patients in our dominant ePharmacy channel"
An epharmacy is an online service that dispenses prescription and over‑the‑counter medicines, often combined with digital tools like ordering apps, home delivery, automated dispensaries, and electronic prescription handling. Think of it as a virtual drugstore that replaces a walk‑in pharmacy with software and logistics, making access to medicines faster and more trackable. For investors, epharmacies matter because they change how medications are sold, can scale digitally, and may affect margins, customer reach, and regulatory risk across the healthcare supply chain.
marketing authorization application regulatory
"LENZ submitted a Marketing Authorization Application (“MAA”)"
A marketing authorization application is a formal request submitted to a government regulator asking permission to sell a prescription medicine or medical product in a country or region. Think of it like asking for a business license after showing evidence the product is safe and works; investors care because approval determines whether the product can generate sales, how soon revenue starts, and how much regulatory risk and uncertainty remains.
mhra regulatory
"the United Kingdom's Medicines and Healthcare products Regulatory Agency"
The MHRA is the United Kingdom’s government agency that checks and approves medicines, medical devices and vaccines before they can be sold, and monitors their safety once on the market. For investors, MHRA decisions act like a building inspector’s sign-off or a traffic controller’s clearance—approval clears the way for sales and revenue, while safety warnings, recalls or delays can slow launches, raise costs or hurt a product’s commercial prospects.
new drug submission regulatory
"upon the submission of its New Drug Submission to Health Canada"
A new drug submission is a formal package of scientific data and paperwork sent to a health authority to request permission to sell a medicine. For investors it signals a key milestone: approval opens the door to sales and revenue, while rejection or delays can cut expected value — think of it like applying for a building permit that determines whether and when a new product can be put on the market.
miotic medical
"VIZZ is a predominantly pupil selective miotic"
A miotic is a drug or agent that causes the pupil of the eye to constrict (get smaller), producing miosis. Think of it like closing the aperture on a camera lens to reduce the amount of light entering the eye; this effect is used in treatments for conditions such as glaucoma and during certain eye procedures. Investors may encounter the term in drug labels, clinical trial results, or regulatory filings because miotic activity describes a drug’s mechanism, potential side effects, and target market.

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

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Q2 2026 total revenue of $5.5 million from VIZZ product sales and global license agreements

Strong patient persistence, with over 60% of patients in our dominant ePharmacy channel purchasing multiple monthly packs since launch, tracking to five packs annually

VIZZ prescription growth accelerated with launch of telehealth channel in July 2026

Management to host conference call today, August 11, 2026, at 4:30 p.m. EDT

SAN DIEGO, Aug. 11, 2026 (GLOBE NEWSWIRE) -- LENZ Therapeutics, Inc. (Nasdaq: LENZ or “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 reported financial results for the second quarter ended June 30, 2026, and recent corporate highlights.

“We are encouraged by the early refill behavior we are seeing with VIZZ. The majority of ePharmacy patients have purchased multiple monthly packs since launch, and among those patients, our Q4 2025 and Q1 2026 cohorts are tracking to average annualized utilization of five packs per patient. These trends reinforce the value VIZZ is delivering in the real world,” said Eef Schimmelpennink, President and Chief Executive Officer of LENZ Therapeutics. “Our focus is now on bringing more consumers into the category and making access as seamless as possible. Through telehealth, eligible consumers can be evaluated online by an independent licensed eye care professional and, if prescribed, receive VIZZ at home. Together with our national ‘Tired of Reading Glasses’ campaign, telehealth is designed to more readily convert awareness into adoption. While it is still early, the initial indicators are encouraging, and we believe we are building the foundation for sustained growth driven by consumers.”

Second Quarter 2026 and Recent Corporate Highlights

Commercial Launch

  • Q2 2026 product revenues of over $1.7 million on approximately 27,000 packs sold, a 9% increase over Q1 2026.
  • Over 60% of ePharmacy patients have purchased more than one monthly pack of VIZZ since launch; encouraging early average projected refill rates from those starting VIZZ in Q4 2025 and Q1 2026 of 5 packs per year.
  • Broad uptake by eye care professionals (“ECPs”), with over 13,000 unique prescribers from launch through Q2 2026, with approximately 75% prescribing multiple times.
  • In July 2026, launched a telehealth prescribing option to accelerate patient access to VIZZ, offering patients the convenience of an integrated online evaluation by independent licensed eye care providers, e-pharmacy prescription fulfillment, and home delivery, in addition to existing access through eye care professionals.
  • In July 2026, launched a nationwide TV advertising campaign featuring brand spokesperson Sarah Jessica Parker. 

Advancing Global Commercialization Strategy and Expanding International Partnerships

  • In April 2026, LENZ 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 for the treatment of presbyopia in adults. The MHRA submission followed validation of the VIZZ MAA by the European Medicines Agency in March 2026.
  • In June 2026, LENZ announced an exclusive license and commercialization agreement with Arrotex Pharmaceuticals to register and commercialize VIZZ for the treatment of presbyopia in Australia and New Zealand, its fifth ex-U.S. commercialization partnership. Under the terms of the agreement, LENZ received an upfront payment and is eligible to receive a mid double-digit profit share of gross margin from product sales in Australia and New Zealand.
  • In June 2026, LENZ achieved its first regulatory milestone under the License and Commercialization Agreement with Laboratoires Théa upon the submission of its New Drug Submission to Health Canada for the review and approval of VIZZ for the treatment of presbyopia in adults in Canada. Under the terms of the agreement, LENZ is eligible to receive up to $65 million in remaining regulatory and commercial milestone payments, as well as tiered, double-digit royalties on future net sales in Canada.
  • In June 2026, Everest Medicines entered into an Asset Purchase Agreement with CORXEL Pharmaceuticals to acquire the rights to develop, manufacture, and commercialize VIZZ (LNZ100) in Greater China. 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 has received the first of multiple potential milestone payments under this sublicensing arrangement in connection with the execution of the agreement between CORXEL and Everest.
  • In July 2026, under the exclusive distribution agreement with Lunatus for the Middle East region, the MAA was submitted under the Saudi Food and Drug Authority’s Abridged Pathway for the treatment of presbyopia in the Kingdom of Saudi Arabia. This submission represents the ninth ex-U.S. regulatory filing for VIZZ.

Financial Results for Three and Six Months Ended June 30, 2026

Cash Position: Cash, cash equivalents and marketable securities were $220.0 million as of June 30, 2026.

Product Sales, net: Product sales, net was $1.7 million and $3.4 million for the three and six months ended June 30, 2026, respectively, driven by approximately 27,000 and 52,000 packs sold and delivered to the customer in the respective periods. We had no product sales during the three and six months ended June 30, 2025.

License Revenue: License revenue was $3.8 million and $4.0 million for the three and six months ended June 30, 2026 including a $2.5 million regulatory milestone reached under the Théa license agreement and $1.25 million in sublicense revenue related to the asset purchase agreement by Everest Medicines to acquire the rights to VIZZ in Greater China during the three months ended June 30, 2026, and the upfront payment under the Lunatus exclusive distribution agreement in the six months ended June 30, 2026. License revenue was $5.0 million during the same periods in 2025 related to the upfront payment under the Lotus license agreement.

Cost of Sales: Cost of sales was $0.3 million and $1.4 million for the three and six months ended June 30, 2026, respectively. Direct product cost of sales in connection with the sales of VIZZ was $0.3 million for the three and six months ended June 30, 2026. Total cost of sales during the six months ended June 30, 2026 was comprised primarily of non-recurring events recognized in the first quarter related to a manufacturing process transition and unrelated to product sales. There was no cost of sales during the three and six months ended June 30, 2025.

Selling, General and Administrative (“SG&A”) Expenses: SG&A expenses increased to $39.4 million and $84.3 million for the three and six months ended June 30, 2026, compared to $12.8 million and $23.9 million during the same respective periods in 2025, primarily driven by our launch investment, with increases in commercial marketing, advertising, sales infrastructure expenses, and personnel-related expenses due to a growth in headcount, including the hiring of our sales force. These amounts include non-cash stock-based compensation expense of $4.4 million and $8.7 million for the three and six months ended June 30, 2026, respectively, and $2.1 million and $4.0 million for the three and six months ended June 30, 2025, respectively.

Research and Development (“R&D”) Expenses: There were no R&D expenses for the three and six months ended June 30, 2026, compared to $9.1 million and $14.9 million during the same respective periods in 2025 due to the FDA approval of VIZZ in July 2025.

Net Loss: Net loss for the three and six months ended June 30, 2026 was $31.9 million and $73.4 million, respectively, or $1.02 and $2.34 per share (basic and diluted), respectively, compared to a net loss of $14.9 million and $29.5 million, respectively, or $0.53 and $1.06 per share (basic and diluted), respectively, during the same periods in 2025.

Conference Call Information
The Company will host a conference call and webcast today, Tuesday, August 11, 2026, at 4:30 p.m. EDT. To participate in the conference call via telephone, dial (800) 715-9871 (Domestic) or (646) 307-1963 (International) and enter code 2922111. The live webcast can be accessed here and on the LENZ Therapeutics website at www.LENZ-tx.com in the Investors & Media section. A replay of the webcast will be available on the Company’s website for 30 days following the event.

About Presbyopia

Presbyopia is the inevitable loss of near vision associated with aging, impacting the daily lives of nearly all people over the age of 45. As people age, the crystalline lens in their eyes gradually hardens and becomes less able to change shape. This loss of elasticity reduces the lens's ability to focus incoming light from near objects onto the retina. Adults over 50 years of age lose, on average, 1.5 lines of near vision every six years. Although the progression of presbyopia is gradual, presbyopes often experience an abrupt change in their daily life as the symptoms become more pronounced starting in their mid-40s, when reading glasses or other corrective aids are suddenly necessary to read text or conduct close-up work. Presbyopia is typically self-diagnosed and self-managed with over-the-counter reading glasses, or managed, after evaluation by an ECP, with prescription reading or bifocal glasses or multifocal contact lenses.

About VIZZ (aceclidine ophthalmic solution) 1.44%

VIZZ (aceclidine ophthalmic solution) 1.44% is a once-daily eye drop developed to restore clear near vision for up to 10 hours. Aceclidine is the sole active ingredient in VIZZ and provides rapid and durable near vision improvement. VIZZ is preservative-free and provided in single-dose vials. VIZZ is a predominantly pupil selective miotic that interacts with the iris with minimal ciliary muscle stimulation. VIZZ causes contraction of the iris sphincter muscle, resulting in a pinhole effect that extends depth of focus to improve vision. For more information, please visit www.VIZZ.com.

VIZZ Indication and Important Safety Information

INDICATION

VIZZ (aceclidine ophthalmic solution) 1.44% is a prescription eye drop used to treat age-related blurry near vision (presbyopia) in adults.

IMPORTANT SAFETY INFORMATION

  • Do not use VIZZ if allergic to any of the ingredients.
  • To help avoid potential eye injury or contamination of the product, do not allow the vial tip to touch the eye or any surfaces. Discard the opened vial immediately after use.
  • Contact lenses should be removed before using VIZZ. After dosing, contact lenses can be reinserted after 10 minutes.
  • If using more than one topical eye medication, the medicines should be administered at least 5 minutes apart.
  • Temporary dim or dark vision may be experienced after using VIZZ. Do not drive or operate machinery if vision is not clear.
  • Seek immediate medical care if sudden onset of flashing lights, floaters, or vision loss is experienced.

ADVERSE REACTIONS

The most common reported adverse reactions of participants were instillation site irritation (20%), dim vision (16%), and headache (13%). Adverse reactions reported in >5% of participants were conjunctival hyperemia (8%) and ocular hyperemia (7%). The majority of adverse reactions were mild, transient, and self-resolving.

For additional information, please see the full Prescribing Information available at http://www.VIZZ.com/full-prescribing-information.pdf

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.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of 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 statements regarding LENZ’s plans regarding the launch of its telehealth platform; the belief that the launch of the telehealth platform alongside LENZ’s sales and marketing activities will help accelerate consumer awareness, access and adoption of VIZZ, and the belief that LENZ is building the foundation for sustained growth driven by consumers; the potential market size for VIZZ; the belief that the telehealth platform will provide a seamless and convenient consumer journey from product interest to home delivery; LENZ’s commercialization plans, including international partnering plans and expectations under existing commercial arrangements, including the potential achievement of milestones under such agreements; projected refill rates; and the quotations of LENZ management. These statements are based on numerous assumptions concerning VIZZ, target markets and involve substantial risks, uncertainties and other factors that may cause actual results, levels of activity, performance or achievement to be materially different from the information expressed or implied by these forward-looking statements, including those risk factors described in the section titled “Risk Factors” in our Quarterly Report on Form 10-Q to be filed for the quarter ended June 30, 2026 and our subsequent filings with the SEC. 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 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


LENZ Therapeutics, Inc.
Selected Balance Sheet Highlights
(in thousands)
    
 June 30, 2026 December 31, 2025
 (unaudited)  
Cash and cash equivalents$24,208 $25,179
Marketable securities 195,795  267,168
Total assets 236,596  305,876
Total liabilities 17,334  21,537
Total stockholders’ equity 219,262  284,339



LENZ Therapeutics, Inc.
Condensed Consolidated Statement of Operations and Comprehensive Loss
(in thousands, except share and per share data)
(unaudited)
    
 Three Months Ended June 30, Six Months Ended June 30,
  2026   2025   2026   2025 
Revenue:       
Product sales, net$1,736  $  $3,387  $ 
License revenue 3,750   5,000   4,000   5,000 
Total revenue 5,486   5,000   7,387   5,000 
Operating expenses:       
Cost of sales 280      1,356    
Selling, general and administrative 39,378   12,796   84,338   23,909 
Research and development    9,061      14,879 
Total operating expenses 39,658   21,857   85,694   38,788 
Loss from operations (34,172)  (16,857)  (78,307)  (33,788)
Other (expense) income:       
Other (expense) income (13)  199   (10)  188 
Interest income 2,270   2,246   4,914   4,569 
Total other income, net 2,257   2,445   4,904   4,757 
Net loss before income taxes (31,915)  (14,412)  (73,403)  (29,031)
Income tax expense 3   500   3   500 
Net loss$(31,918) $(14,912) $(73,406) $(29,531)
Other comprehensive loss:       
Unrealized loss on marketable securities (179)  (85)  (871)  (158)
Comprehensive loss$(32,097) $(14,997) $(74,277) $(29,689)
Net loss per share, basic and diluted$(1.02) $(0.53) $(2.34) $(1.06)
Weighted-average common shares outstanding, basic and diluted 31,374,311   28,079,071   31,363,566   27,804,112 

FAQ

How did LENZ Therapeutics (LENZ) perform financially in Q2 2026?

LENZ reported Q2 2026 revenue of $5.5 million, up from $5.0 million a year earlier. According to LENZ Therapeutics, this included $1.7 million in VIZZ product sales and $3.8 million in license revenue, with a quarterly net loss of $31.9 million.

What were LENZ Therapeutics’ VIZZ sales and prescription metrics in Q2 2026?

VIZZ generated $1.7 million in Q2 2026 product sales from about 27,000 packs. According to LENZ Therapeutics, more than 60% of ePharmacy patients purchased multiple packs, early cohorts are tracking to roughly five packs yearly, and over 13,000 unique prescribers have written prescriptions.

What is LENZ Therapeutics’ cash position as of June 30, 2026 (ticker LENZ)?

LENZ held $220.0 million in cash, cash equivalents and marketable securities at June 30, 2026. According to LENZ Therapeutics, this comprised $24.2 million of cash and equivalents and $195.8 million of marketable securities, supporting ongoing commercialization and partnership activities for VIZZ.

Which international partnerships and milestones did LENZ Therapeutics announce for VIZZ in 2026?

LENZ expanded ex‑U.S. rights through agreements in Australia/New Zealand, Canada, Greater China and the Middle East. According to LENZ Therapeutics, it is eligible for up to $65 million in remaining Canadian milestones and up to $85 million in Greater China milestones, plus royalties and profit share.

How did LENZ Therapeutics’ expenses and net loss change in Q2 2026?

Q2 2026 SG&A expenses rose to $39.4 million, up from $12.8 million in 2025, reflecting launch investments. According to LENZ Therapeutics, R&D dropped to zero after VIZZ approval, and net loss widened to $31.9 million for the quarter and $73.4 million for six months.

What regulatory filings for VIZZ has LENZ Therapeutics made outside the United States by mid-2026?

LENZ has nine ex‑U.S. regulatory filings for VIZZ by July 2026. According to LENZ Therapeutics, recent submissions include a UK MAA, a Health Canada New Drug Submission via Théa, and an MAA under Saudi Arabia’s Abridged Pathway, following earlier EMA validation of the European application.

How is LENZ Therapeutics expanding patient access to VIZZ in the United States?

In July 2026, LENZ introduced a telehealth prescribing option and a national TV campaign. According to LENZ Therapeutics, telehealth enables online evaluation by independent eye care professionals, e‑pharmacy fulfillment, and home delivery, complementing existing in‑office prescribing to help drive VIZZ adoption.