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Vivani Medical Reports First Quarter 2026 Financial Results and Provides Business Update

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Vivani Medical (Nasdaq: VANI) reported Q1 2026 results and a pipeline update. The SLIM-1™ Phase 1 trial of semaglutide implant NPM-139 is expected to start mid-2026, with top-line data by year-end. Vivani held about $28 million in cash and commitments, projected to fund operations through the first half of 2027, and reported a Q1 2026 net loss of $6.8 million. The company is also evaluating paths to separate neuromodulation subsidiary Cortigent into an independent public company.

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Positive

  • Cash and commitments of $28 million fund operations through H1 2027
  • $30.2 million gross capital raised over the last 12 months
  • Q1 2026 financing inflows totaled $9.7 million
  • SLIM-1 Phase 1 trial start targeted for mid-2026
  • Top-line SLIM-1 data anticipated by end of 2026

Negative

  • Q1 2026 net loss was $6.8 million versus $6.3 million
  • Operating cash used in Q1 2026 totaled $6.2 million
  • R&D expense rose to $4.4 million from $4.2 million
  • G&A expense increased to $2.4 million from $2.3 million
  • Other income declined by $0.3 million year over year

News Market Reaction – VANI

+3.45%
+3.45% Session close to close

In the May 14 session, VANI gained 3.45%, reflecting a moderate positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement combines Q1 2026 financials with confirmation of a cash runway into the first half...
Analysis

This announcement combines Q1 2026 financials with confirmation of a cash runway into the first half of 2027, supported by $28 million in cash and commitments and $30.2 million raised over the past year. It reiterates plans for the SLIM-1 Phase 1 semaglutide implant study, a planned Phase 2 in 2027, and potential separation of Cortigent. Investors may track clinical milestones, financing activity, and the structure and timing of any Cortigent transaction.

Key Figures

Cash and commitments: $28 million Gross proceeds raised: $30.2 million Operating cash use: $6.2 million +5 more
8 metrics
Cash and commitments $28 million Cash, cash equivalents, restricted cash and capital commitments; runway into H1 2027
Gross proceeds raised $30.2 million Share purchase agreements and registered direct offerings over last 12 months
Operating cash use $6.2 million Cash used in operating activities for three months ended March 31, 2026
Net loss $6.8 million Net loss for the three months ended March 31, 2026
R&D expense $4.4 million Research and development expense, net of grants, Q1 2026
G&A expense $2.4 million General and administrative expense, net of grants, Q1 2026
Financing cash inflow $9.7 million Cash provided by financing activities in Q1 2026
Investing cash use $3,000 Cash used for property and equipment purchases in Q1 2026

Previous Earnings Reports

5 past events · Latest: Mar 26 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 26 Earnings and update Positive -1.9% Q4 2025 results, NPM-139 progress, financing extending runway into mid-2027.
Nov 13 Earnings and update Positive -11.4% Q3 2025 results, LIBERATE-1 completion and strong NPM-139 preclinical data.
Aug 13 Earnings and financing Positive +0.8% $10M equity financing plus positive NPM-139 and LIBERATE-1 data.
May 13 Earnings and financing Positive -3.8% Q1 2025 results, multiple equity raises and LIBERATE-1 progress.
Mar 31 Full-year results Positive -5.4% 2024 results with GLP-1 implant advances and extended cash runway.

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

Pattern Detected

Earnings and business updates have frequently been followed by negative next-day moves despite highlighting financing and pipeline progress.

Recent Company History

Over the past year, Vivani’s earnings and business updates on Mar 31, 2025, May 13, 2025, Aug 13, 2025, Nov 13, 2025, and Mar 26, 2026 consistently emphasized GLP‑1 implant development, LIBERATE-1 data, and equity financings that extended runway into mid‑2026 and mid‑2027. Yet four of these five earnings events saw negative price reactions within 24 hours. Today’s Q1 2026 update, which again reiterates cash runway into the first half of 2027 and clinical milestones, fits into this pattern of constructive news paired with cautious trading.

Key Terms

phase 1, semaglutide, glp-1, investigational new drug, +4 more
8 terms
phase 1 medical
"Initiation of SLIM-1™ clinical trial, a Phase 1 study of NPM-139..."
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
semaglutide medical
"...a Phase 1 study of NPM-139, a semaglutide implant under development..."
Semaglutide is a medication originally developed to help manage blood sugar levels in people with diabetes, but it also promotes weight loss. It works by mimicking a natural hormone that helps control appetite and insulin release. For investors, its potential to influence healthcare and weight management markets makes it a significant product in the pharmaceutical industry.
glp-1 medical
"...health outcomes otherwise possible with GLP-1 therapies."
GLP-1 (glucagon-like peptide-1) is a natural hormone in the body that helps regulate blood sugar levels and appetite. Its significance to investors lies in its role as the basis for a class of medications that address conditions like type 2 diabetes and obesity, which are large and growing markets. Advances or investments in GLP-1-based treatments can signal opportunities in healthcare innovation and potentially impact pharmaceutical companies’ growth.
investigational new drug regulatory
"Pending positive SLIM-1 clinical results, a pre-IND meeting with the U.S. FDA..."
An investigational new drug is a medication that is still being tested in clinical trials to determine if it is safe and effective for treating a specific condition. For investors, it represents a potential breakthrough that could lead to a new treatment and significant financial gains if successful, but also carries risks since it has not yet been approved for widespread use.
registered direct offering financial
"...$2.2 million in net proceeds from a registered direct offering with a placement agent..."
A registered direct offering is a way for a company to sell new shares of its stock directly to select investors with regulatory approval. This method allows the company to raise funds quickly and efficiently without needing a public auction, similar to offering exclusive access to a limited number of buyers. For investors, it often provides an opportunity to purchase shares at a favorable price, while giving the company immediate access to capital.
form s-1 regulatory
"Cortigent Inc. (“Cortigent”), a wholly owned subsidiary of the Company, filed its most recent amendment to its registration statement on Form S-1..."
A Form S-1 is the registration filing a company submits to the U.S. Securities and Exchange Commission when it plans to offer stock to the public, most commonly for an initial public offering. Think of it as the company’s full disclosure packet or blueprint: it contains audited financials, business description, management background, risk factors and details of the offering, giving investors the information needed to judge the company’s financial health and potential risks before buying shares.
form 10 regulatory
"...including a spin-off to be registered on a Form 10 and an IPO to be registered on a Form S-1..."
Form 10 is a U.S. Securities and Exchange Commission filing companies use to register their securities and become subject to public reporting requirements, delivering a comprehensive package of business descriptions, audited financial statements, management information and risk factors. For investors it matters because it creates a standardized, permanent dossier on a company—like a full inspection and disclosure packet when buying a house—so you can assess finances, risks and management and compare firms reliably.
ipo financial
"...including a spin-off to be registered on a Form 10 and an IPO to be registered on a Form S-1..."
An initial public offering (IPO) is the process by which a private company sells its shares to the public for the first time, making its ownership available on the stock market. This allows the company to raise money from a wide range of investors to fund growth or other goals. For investors, an IPO offers a chance to buy into a company early in its public journey, potentially benefiting if the company grows in value.
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Initiation of SLIM-1™ clinical trial, a Phase 1 study of NPM-139, a semaglutide implant under development for chronic weight management, on track for mid-year 2026

$28 million in cash, cash equivalents, restricted cash and capital commitments expected to fund current operating plan through the first half of 2027

ALAMEDA, Calif., May 13, 2026 (GLOBE NEWSWIRE) -- Vivani Medical, Inc. (Nasdaq: VANI) (“Vivani” or the “Company”), a clinical-stage biopharmaceutical company developing miniature, ultra long-acting subdermal drug implants utilizing its proprietary NanoPortal™ technology, today reported financial results for the first quarter ended March 31, 2026, and provided a business update.

Vivani Chief Executive Officer Adam Mendelsohn, Ph.D., stated, “I’m very pleased with the progress our team made in the first quarter. We are on track to initiate the first study in our SLIM™ Clinical Program (Semaglutide ultra Long-acting IMplant in obesity). Our Phase 1 study of NPM-139, also known as SLIM-1, will be conducted in Australia and is anticipated to start mid-year 2026. Based on our prior experience with the execution of our first-in-human LIBERATE-1 clinical trial in 2025, we anticipate top-line SLIM-1 results by the end of this year. In parallel, we continue to make good progress on our next generation NPM-139 implant configuration, which is designed to accommodate larger doses of semaglutide in-line with Wegovy® dosing. Pending positive SLIM-1 clinical results, a pre-IND meeting with the U.S. FDA and filing of an Investigational New Drug Application, we aim to launch our Phase 2 study in the SLIM program in 2027. Our strong financial position, with a cash runway through the first half of 2027, underscores our ability to deliver on these milestones and drive meaningful progress in addressing critical healthcare needs."

Dr. Mendelsohn continued: “As the obesity treatment landscape continues to evolve, challenges associated with medication adherence have emerged as a clear and undeniable barrier to the full realization of health outcomes otherwise possible with GLP-1 therapies. These challenges affect patients on injectable and oral GLP-1 options alike. With the potential to provide steady and continuous GLP-1 delivery over periods of 6 months, 12 months, or more, our NanoPortal™ technology is uniquely designed to solve for these challenges while still allowing for patients to stop exposure to the drug on a timeline similar to the current weekly injectables. We’re confident that its distinct advantages will become increasingly apparent as adherence-related data for the GLP-1 class continues to accumulate, and as adherence-related costs for patients, payors, and health systems continue to mount.”

Recent Business Highlights

The Company plans to continue exploring opportunities for Vivani’s stockholders to potentially realize value in its neuromodulation assets. Cortigent Inc. (“Cortigent”), a wholly owned subsidiary of the Company, filed its most recent amendment to its registration statement on Form S-1 on May 13, 2026.

Including multiple share purchase agreements and registered direct offerings entered into in the last 12 months, Vivani has raised $30.2 million in gross proceeds. Current cash, cash equivalents and capital commitments as of March 31, 2026, are expected to fund operations through the first half of 2027.

Upcoming Anticipated Milestones

Initiation of SLIM-1, a Phase 1 study of low-dose NPM-139, Vivani’s miniature, ultra long-acting semaglutide implant under development for chronic weight management, anticipated mid-2026 and top-line results are projected by the end of 2026.

Investigational New Drug (“IND”) Application for NPM-139 to support initiation of the proposed Phase 2 dose-ranging study of this semaglutide implant planned for 2027.

Transition of Cortigent into an independent, publicly traded company. Currently, multiple approaches, including a spin-off to be registered on a Form 10 and an IPO to be registered on a Form S-1 are under consideration.

First Quarter 2026 Financial Results

Cash: During the three months ended March 31, 2026, Vivani used $6.2 million of cash in operating activities, consisting primarily of a net loss of $6.8 million, partially offset by $0.1 million from a net change in operating assets and liabilities, and non-cash items totaling $0.5 million for stock-based compensation, lease expense, and depreciation of property and equipment. Cash used for investing activities during the three months ended March 31, 2026 was $3,000 for the purchase of property and equipment. Cash provided by financing activities was $9.7 million during the three months ended March 31, 2026, primarily attributable to $2.2 million in net proceeds from a registered direct offering with a placement agent and $7.6 million in net proceeds from other securities purchase agreements with an affiliate of one of its independent directors and another investor.

Research and development expense, net of grants. Research and development expense, net of grants, during the three months ended March 31, 2026 was $4.4 million, compared to $4.2 million during the three months ended March 31, 2025. The increase of $0.2 million, or 4%, was primarily attributable to the increase in both the clinical trial related expense and development expense. 

General and administrative expense, net of grants. General and administrative expense, net of grants, during the three months ended March 31, 2026 was $2.4 million, compared to $2.3 million during the three months ended March 31, 2025. The increase of $0.1 million, or 4%, was primarily attributable to an increase in professional services fees.

Other income, net. Other income, net during the three months ended March 31, 2026 was insignificant, compared to $0.3 million during the three months ended March 31, 2025. The decrease of $0.3 million was primarily attributable to lower interest income being earned on deposits and the write-off of the accumulated other comprehensive income related to foreign currency translation balance of the Neurostimulation Division’s Switzerland subsidiary effectively closed in 2025, partially offset by an increase in research and development rebates earned.

Net loss. For the foregoing reasons, Vivani had a net loss of $6.8 million during the three months ended March 31, 2026 compared to $6.3 million during the three months ended March 31, 2025.

About Vivani Medical, Inc.

Vivani is a clinical stage biopharmaceutical company that develops miniature, ultra long-acting subdermal drug implant candidates utilizing its proprietary NanoPortal™ technology, which is designed to enable reversible, ultra long-acting, near constant-rate delivery of a broad range of medicines to treat chronic diseases. Vivani is leveraging its proprietary NanoPortal™ platform, to develop biopharmaceutical implants designed to deliver drug molecules steadily over extended periods of time with the goal of guaranteeing adherence and improving patient tolerance to their medication. Vivani is developing a portfolio of GLP-1 based implants for metabolic diseases including obesity and type-2 diabetes. These NanoPortal implants are designed to provide patients with the opportunity to realize the full potential benefit of their medication by avoiding the numerous challenges associated with the daily or weekly administration of orals and injectables, including tolerability issues and loss of efficacy. Medication non-adherence occurs when patients do not take their medication as prescribed. This affects an alarming number of patients, approximately 50%, including those taking daily pills. For more information, please visit: www.vivani.com.

About Cortigent, Inc.

Cortigent, Inc., a wholly owned subsidiary of Vivani, is developing brain implant devices to help patients recover critical body functions. Its patent-protected precision neurostimulation technology platform leverages neuroscience and proprietary microelectronics to create advanced medical devices. Vivani’s predecessor, Second Sight Medical Products, previously marketed Argus® II, the first and only medical device to obtain FDA approval to treat a rare form of blindness. This innovative device has helped hundreds of profoundly blind patients to achieve meaningful visual perception. Cortigent’s next generation investigational system, the Orion® cortical stimulation system, has been designed to treat blindness caused by common conditions including glaucoma and diabetic retinopathy. Orion has an FDA Breakthrough Device designation, completed a 6-year Early Feasibility Study in 2025 with promising safety and efficacy results and is covered by an extensive intellectual property estate. Cortigent is also applying its core technology to improving recovery of arm and hand motion in patients with paralysis due to stroke. For more information and patient videos, please visit: www.cortigent.com.

Forward-Looking Statements

This press release contains certain “forward-looking statements” within the meaning of the “safe harbor” provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward looking statements can be identified by words such as: “target,” “believe,” “expect,” “will,” “may,” “anticipate,” “estimate,” “would,” “positioned,” “future,” and other similar expressions that are used in this press release, including express or implied statements regarding Vivani’s business, products in development, including the therapeutic potential and planned development thereof (including, for example, initiation of Phase 1 study of NPM-139, announcement of topline results, and launch of Phase 2 study in the SLIM clinical program), Vivani’s plans with respect to Cortigent and its ability to spin-out Cortigent, as well as statements regarding Vivani’s technology, strategy, cash position and financial runway, among others. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on Vivani’s current beliefs, expectations, and assumptions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of Vivani’s control. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements, including, without limitation, risks related to developing subdermal implants and conducting clinical trials; risks related to the biopharmaceutical industry generally; risks related to the Cortigent spin-off, including that it will not be completed in a timely manner or at all, that conditions to spin-out will not be satisfied, risks related to the tax treatment of the spin-off, and uncertainty of whether the anticipated benefits of the spin-off can be achieved; as well as more general risks of unexpected costs or delays in conducting its business; and risks and uncertainties associated with the development and commercialization of products and product candidates that may impact or alter anticipated business plans, strategies and objectives; among others. There may be additional risks that the Company or Cortigent consider immaterial, or which are unknown. A further list and description of risks and uncertainties can be found in the Company’s most recent Quarterly Report on Form 10-Q filed with the U.S. Securities and Exchange Commission (“SEC”) on May 13, 2026, as updated by the future filings with the SEC. Actual results and outcomes may differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Any forward-looking statement made by Vivani in this press release is based only on information currently available and speak only as of the date of this press release. Vivani undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of added information, future developments or otherwise, except as required by law.

Company Contacts:

Company Contact:
Donald Dwyer
Chief Business Officer
info@vivani.com
(415) 506-8462

Investor and Media Relations Contact:
Jami Taylor
Investor and Media Relations Advisor
investors@vivani.com
(415) 506-8462

VIVANI MEDICAL, INC.
AND SUBSIDIARIES

Condensed Consolidated Balance Sheets (Unaudited)
(In thousands, except per share data)
    
 March 31, December 31,
 2026 2025
ASSETS     
CURRENT ASSETS:     
Cash and cash equivalents$19,749 $16,232
Receivables 12  -
R&D tax credit incentive receivable 685  654
Prepaid expenses and other current assets 1,102  1,012
Total current assets 21,548  17,898
Property and equipment, net 2,752  2,879
Operating lease right-of-use assets, net 16,616  17,230
Restricted cash 1,338  1,338
Deposits and other assets 99  48
TOTAL ASSETS$42,353 $39,393
LIABILITIES AND STOCKHOLDERS’ EQUITY     
CURRENT LIABILITIES:     
Accounts payable$1,465 $1,032
Accrued expenses 1,504  1,736
Litigation accrual 1,675  1,675
Accrued compensation expense 349  365
Lease liability, current portion 1,782
  1,794
Total current liabilities 6,775  6,602
Lease liability, noncurrent portion 16,493  17,061
TOTAL LIABILITIES 23,268  23,663
Commitments and contingencies (Note 12)     
Stockholders’ equity:     
Common stock, par value $0.0001 per share; 300,000 shares authorized; shares issued and outstanding: 84,648 and 76,428 at March 31, 2026 and December 31, 2025, respectively 8  8
Additional paid-in capital 174,358  164,225
Accumulated other comprehensive income 32  30
Accumulated deficit (155,313)  (148,533)
TOTAL STOCKHOLDERS' EQUITY 19,085  15,730
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY$42,353 $39,393


VIVANI MEDICAL, INC.
AND SUBSIDIARIES

Condensed Consolidated Statements of Operations (Unaudited)
(In thousands, except per share data)
  
 Three Months Ended March 31,
 2026 2025
Operating expenses:     
Research and development, net of grants$4,390 $4,217
General and administrative, net of grants 2,427  2,340
Total operating expenses, net 6,817  6,557
Loss from operations (6,817)  (6,557)
Other income, net 37  255
Net loss$(6,780) $(6,302)
Net loss per common share - basic and diluted$(0.08) $(0.11)
Weighted average common shares outstanding - basic and diluted 81,269  59,236



FAQ

What financial results did Vivani Medical (Nasdaq: VANI) report for Q1 2026?

Vivani reported a Q1 2026 net loss of $6.8 million. According to Vivani, operating cash use was $6.2 million, R&D expense was $4.4 million, and G&A expense was $2.4 million, all slightly higher than the same period in 2025.

When will Vivani Medical (VANI) start the SLIM-1 Phase 1 trial of NPM-139?

Vivani expects to initiate the SLIM-1 Phase 1 study in mid-2026. According to Vivani, the trial will evaluate a low-dose semaglutide implant for chronic weight management, with top-line SLIM-1 results projected by the end of 2026.

How long will Vivani Medical's (VANI) cash last based on the Q1 2026 update?

Vivani projects its cash runway extends through the first half of 2027. According to Vivani, it had about $28 million in cash, cash equivalents, restricted cash and capital commitments as of March 31, 2026, supporting its current operating plan.

What are the key SLIM program milestones Vivani Medical (VANI) targets through 2027?

Vivani plans SLIM-1 Phase 1 initiation mid-2026 and top-line data by year-end. According to Vivani, an IND filing for NPM-139 is planned to enable a Phase 2 dose-ranging study in 2027 within the SLIM obesity program.

What is Vivani Medical (VANI) planning for its Cortigent neuromodulation business?

Vivani is exploring ways for stockholders to realize value from Cortigent. According to Vivani, options include a spin-off registered on Form 10 or an IPO registered on Form S-1, with an amended Cortigent S-1 filed May 13, 2026.

How much capital has Vivani Medical (VANI) raised recently, and from which activities?

Vivani has raised $30.2 million in gross proceeds over the last 12 months. According to Vivani, Q1 2026 financing cash inflows were $9.7 million from a registered direct offering and additional securities purchase agreements with investors.