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Vyome Holdings (Nasdaq: HIND) Q1 2026 loss widens while cash balance grows

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Vyome Holdings reported first quarter 2026 results and highlighted progress on its clinical pipeline and balance sheet. The company is advancing VT-1953 for malignant fungating wounds and has submitted an application to the FDA for orphan drug designation and proposals for next-stage development planning.

Cash and cash equivalents were $8.8 million as of March 31, 2026, up from $5.0 million at December 31, 2025, with total assets increasing to $10.2 million. Total stockholders’ equity rose to $8.0 million from $3.8 million, and management emphasized having no debt, no preferred stock, and no toxic financing instruments.

For the quarter ended March 31, 2026, Vyome generated revenue of $31,591, down from $198,581 a year earlier, and recorded a net loss of $985,521 versus $293,974 in the prior-year period, driven by higher operating expenses of $1.15 million. The company plans a conference call and webcast on June 3, 2026, to discuss these results.

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Insights

Vyome’s cash position improved, but revenue fell and losses widened.

Vyome Holdings is still in the clinical stage, so quarterly volatility is expected. Cash and cash equivalents rose to $8.8 million and total equity to $8.0 million, giving the company more room to fund development.

At the same time, revenue declined to $31,591 from $198,581, while operating expenses increased to $1.15 million. This pushed net loss to $985,521. These shifts reflect heavier investment and limited near-term revenue rather than a commercial contraction.

Management underscored a capital structure with no debt, preferred stock, or toxic financing and highlighted regulatory momentum around VT-1953, including an FDA orphan drug designation application. Future company filings may clarify how long current cash can support planned development activities.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Cash and cash equivalents $8,795,783 As of March 31, 2026
Cash and cash equivalents prior $4,982,333 As of December 31, 2025
Total stockholders’ equity $8,041,321 As of March 31, 2026
Revenue $31,591 Three months ended March 31, 2026
Revenue prior-year quarter $198,581 Three months ended March 31, 2025
Net loss $985,521 Three months ended March 31, 2026
Net loss prior-year quarter $293,974 Three months ended March 31, 2025
Operating expenses $1,146,585 Three months ended March 31, 2026
orphan drug designation regulatory
"We submitted to the FDA an application for the approval of orphan drug designation status"
Orphan drug designation is a special status given to medicines developed to treat rare diseases affecting only a small number of people. This status often provides benefits like faster approval processes and financial incentives, making it more attractive for companies to develop these drugs. For investors, it signals potential for exclusive market rights and reduced competition, which can impact the drug’s profitability.
malignant fungating wounds medical
"VT-1953 addresses a major unmet need in malignant fungating wounds"
Malignant fungating wounds are open, often damaged patches of skin and tissue that develop when an advancing cancer breaks through the skin, leading to pain, odor, bleeding and high infection risk. Investors care because these wounds drive demand for specialized wound-care products, palliative drugs, medical devices and home care services; like a house with a chronic leak, they create ongoing treatment costs, regulatory scrutiny and potential market opportunity for better therapies.
immuno-inflammatory medical
"focused on immuno-inflammatory and rare disease conditions"
Immuno-inflammatory describes processes in which the immune system causes or controls inflammation in the body — a coordinated response that can protect against infection but also drive chronic illness when overactive. Investors care because many drugs, devices and diagnostics target these pathways; success or failure in clinical trials, approvals or reimbursements for immuno-inflammatory therapies can quickly change a company’s revenue outlook, valuation and market opportunity, like fixing a faulty fire alarm that either prevents disaster or keeps dousing the house.
forward-looking statements regulatory
"Certain statements made in this press release are “forward-looking statements”"
Forward-looking statements are predictions or plans that companies share about what they expect to happen in the future, like estimating sales or profits. They matter because they help investors understand a company's outlook, but since they are based on guesses and assumptions, they can sometimes be wrong.
Private Securities Litigation Reform Act of 1995 regulatory
"within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995"
toxic financing instruments financial
"no debt, no preferred stock, and no toxic financing instruments"
Revenue $31,591
Net loss $985,521
Cash and cash equivalents $8,795,783
false 0001427570 0001427570 2026-05-28 2026-05-28 iso4217:USD xbrli:shares iso4217:USD xbrli:shares

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, DC 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the

Securities Exchange Act of 1934

 

Date of report (Date of earliest event reported): May 28, 2026

 

VYOME HOLDINGS, INC.

(Exact name of registrant as specified in its charter)

 

Delaware   1-37897   26-1828101
(State or other jurisdiction
of incorporation)
  (Commission File Number)   (IRS Employer
Identification No.)

 

Harvard Square, One Mifflin Place, Suite 400

Cambridge, MA

  02138
(Address of principal executive offices)   (Zip Code)

 

(949) 429-6680

(Registrant’s telephone number, including area code)

 

Not Applicable

(Former name or former address, if changed since last report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
Common stock, par value $0.001 per share   HIND   The Nasdaq Capital Market

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 

 

 

 

 

 

Item 2.02 Results of Operations and Financial Condition

 

On May 28, 2026, Vyome Holdings, Inc. issued a press release announcing its financial results for its first fiscal quarter ended March 31, 2026. The full text of the press release is furnished herewith as Exhibit 99.1.

 

The information disclosed under this Item 2.02, including Exhibit 99.1 hereto, is being furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), nor shall it be incorporated by reference into any registration statement or other document pursuant to the Securities Act of 1933, as amended, or the Exchange Act except as expressly set forth in such filing.

 

Item 9.01 Financial Statements and Exhibits

 

Exhibit No.   Description
99.1   Press Release dated May 28, 2026
104   Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

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SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  VYOME HOLDINGS, INC.
   
May 29, 2026 By: /s/ Venkat Nelabhotla
  Name:  Venkat Nelabhotla
  Title: President & Chief Executive Officer

 

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Exhibit 99.1

 

Vyome Holdings Reports First Quarter 2026 Results With Key FDA Filings and Strong Balance Sheet

 

Vyome has signed an agreement with Impetis Biosciences Limited, a TATA Enterprise, to in-license two selective JAK inhibitor assets, opening access to a large and growing ~$57B global market1

 

VT-1953 regulatory submissions to the FDA for Orphan Drug Designation status and proposals for constructive FDA guidance on the next steps of development

 

Company ends Q1 2026 with approximately $8.8 million in cash and cash equivalents while maintaining a clean capital structure with no debt, no preferred stock, and no toxic financing instruments

 

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Vyome Holdings, Inc. (Nasdaq: HIND)(“Vyome”), a clinical-stage biopharmaceutical company focused on immuno-inflammatory and rare disease conditions, today reports financial results for the first quarter ended March 31, 2026, and provides a corporate update.

 

Krishna Gupta, Chairman of Vyome, said, “Over the last several quarters, Vyome has executed with focus and discipline, advancing differentiated programs in areas of significant unmet medical need focused on inflammatory disorders. Inflammation remains one of the world’s largest problems, and we believe Vyome is well positioned for long-term value creation. We continue to strengthen our scientific, operational, and governance foundation while remaining highly disciplined on capital structure and shareholder alignment.”

 

Venkat Nelabhotla, CEO of Vyome, stated, “We continue to advance VT-1953 toward pivotal-stage readiness while maintaining a strong focus on disciplined execution, regulatory engagement, manufacturing preparedness, and financial stewardship. We submitted to the FDA an application for the approval of orphan drug designation status and proposals across several areas of the next stages of development readiness, and continue to believe VT-1953 addresses a major unmet need in malignant fungating wounds, where there are currently no FDA-approved therapies specifically addressing the condition.”

 

“Importantly, we have continued to preserve what we believe is one of the Company’s key differentiators: a clean and disciplined capital structure with no debt, no preferred stock, and no toxic financing instruments. We remain focused on creating long-term shareholder value while advancing our immuno-inflammatory and rare disease strategy,” concluded Mr. Nelabhotla.

 

 

1https://www.researchandmarkets.com/report/jak-inhibitor?srsltid=AfmBOoonOb9NkQoIR8mj_k-Nb-XVnCirMY73UDt2qTp7k7IFfvbe41hi

 

 

 

 

First Quarter 2026 and Recent Corporate Highlights

 

Regulatory submissions with the FDA related to VT-1953 pivotal development readiness, including discussions involving manufacturing, toxicology, pharmacokinetic requirements, and clinical development considerations. Filed an Orphan Drug Designation application with the FDA

 

Continued advancement of VT-1953 for malignant fungating wounds, a condition associated with significant unmet medical need and no FDA-approved therapies specifically addressing the condition.

 

Raised approximately $5.29 million in gross proceeds through the sale of 1,089,545 common shares on January 27, 2026, at an average price of $5.00 per share, representing a 59.2% premium to the prior day’s closing price, with total dilution to existing shareholders of approximately 15%

 

Continued scientific and translational activities supporting VT-1908 and broader immuno-inflammatory initiatives

 

Presented positive VT-1953 Phase 2 clinical study data at the prestigious American Association for Cancer Research (AACR) 2026

 

Entered into a strategic in-licensing agreement with Impetis Biosciences Limited, a TATA Enterprise, for selective JAK inhibitor assets under a capital-light structure with payments at commercialization, and development using non-dilutive pathways

 

Financial Results for the Quarter Ended March 31, 2026

 

Cash and cash equivalents were approximately $8.8 million as of March 31, 2026, compared with approximately $5.0 million as of December 31, 2025

 

Total assets were approximately $10.2 million as of March 31, 2026

 

Total stockholders’ equity was approximately $8.0 million as of March 31, 2026

 

Total operating expenses for the quarter ended March 31, 2026, were approximately $1.1 million, including approximately $666,000 in research and development expenses and approximately $478,000 in selling, general, and administrative expenses

 

Net loss attributable to common shareholders for the quarter ended March 31, 2026, was approximately $963,000, or approximately $0.15 per basic and diluted share

 

The Company will also host a conference call and webcast on Wednesday, June 3, 2026, at 11:00 a.m. ET to discuss the results. To access the webcast, please use the following link: https://event.choruscall.com/mediaframe/webcast.html?webcastid=531gpp9T or dial in at 1-877-317-6789 (U.S./Canada toll-free) or +1-412-317-6789 (international).

 

A replay will be available on the Company Website.

 

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About Vyome Holdings, Inc.:

 

Vyome is building the world’s premier platform spanning the US-India innovation corridor. Vyome’s immediate focus is on leveraging its clinical-stage assets to transform the lives of patients with immuno-inflammatory conditions. By applying groundbreaking science and its unique positioning, Vyome seeks to deliver lasting value to shareholders in a hyper cost-efficient manner while upholding global standards of quality and safety.

 

To learn more, please visit  www.vyometx.com

 

Forward-Looking Statements

 

Certain statements made in this press release are “forward-looking statements” within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words such as “target,” “believe,” “expect,” “will,” “shall,” “may,” “anticipate,” “estimate,” “would,” “positioned,” “future,” “forecast,” “intend,” “plan,” “project,” “outlook,” and other similar expressions that predict or indicate future events or trends or that are not statements of historical matters. Such statements include, but are not limited to, statements contained in this press release relating to Vyome’s business strategy, the anticipated timing and outcome of regulatory submissions to the FDA, Vyome’s future operating results, and liquidity and capital resources outlook. Forward-looking statements are based on Vyome’s current expectations and assumptions regarding Vyome’s business, the economy, and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks, and changes in circumstances that are difficult to predict. Vyome’s actual results may differ materially from those contemplated by the forward-looking statements. They are neither statements of historical fact nor guarantees of assurance of future performance. Vyome cautions you, therefore, against relying on any of these forward-looking statements. Important factors that could cause actual results to differ materially from those in the forward-looking statements include, without limitation, Vyome’s ability to raise capital to fund continuing operations; our ability to protect Vyome’s intellectual property rights; the impact of any infringement actions or other litigation brought against Vyome; competition from other providers and products; Vyome’s ability to develop and commercialize products and services; changes in government regulation; and other factors relating to Vyome’s industry, operations and results of operations described in the Vyome’s Annual Report on Form 10-K for the year ended December 31, 2025, our Quarterly Reports on Form 10-Q, our Current Reports on Form 8-K and subsequent filings with the Securities and Exchange Commission. Actual results may differ significantly from those anticipated, believed, estimated, expected, intended, or planned. Factors or events that could cause Vyome’s actual results to differ may emerge from time to time, and it is not possible for Vyome to predict all of them. Vyome cannot guarantee future results, levels of activity, performance, or achievements. Vyome assumes no obligation to update any forward-looking statements in order to reflect any event or circumstance that may arise after the date of this release, except as may be required under applicable securities law.

 

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SUMMARY FINANCIAL STATEMENTS

 

SUMMARY OF CONDENSED CONSOLIDATED BALANCE SHEETS AS OF

 

   March 31,
2026
   December 31,
2025
 
Cash and cash equivalents  $8,795,783   $4,982,333 
Other current assets   366,799    455,988 
Long term assets   1,022,864    1,058,856 
Total assets  $10,185,446   $6,497,177 
           
Liabilities  $2,144,125   $2,735,160 
Total Stockholders’ equity (deficit)   8,041,321    3,762,017 
Total liabilities and stockholders’ equity  $10,185,446   $6,497,177 

 

SUMMARY OF CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

 

   Three
months
ended
March 31,
2026
   Three
months
ended
March 31,
2025
 
Revenues  $31,591   $198,581 
Cost of goods sold   (14,946)   (44,162)
           
Gross profit   16,645    154,419 
           
Operating expenses   1,146,585    353,417 
Operating loss   (1,129,940)   (198,998)
           
Interest and other expenses, net   144,419    (94,976)
           
Net loss  $(985,521)  $(293,974)

 

Contacts

 

Media:

contact@vyometx.com

 

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FAQ

How did Vyome Holdings (HIND) perform financially in Q1 2026?

Vyome reported Q1 2026 revenue of $31,591 and a net loss of $985,521. Higher operating expenses of $1,146,585 and lower revenue versus 2025 drove the wider loss as the company invested in its clinical-stage programs.

What changed in Vyome Holdings’ balance sheet as of March 31, 2026?

As of March 31, 2026, Vyome held $8,795,783 in cash and cash equivalents, up from $4,982,333 at year-end 2025. Total assets rose to $10,185,446, and stockholders’ equity increased to $8,041,321, reflecting a stronger balance sheet position.

What did Vyome Holdings say about its capital structure in this update?

Management highlighted what it views as a key differentiator: a clean capital structure with no debt, no preferred stock, and no toxic financing instruments. The company emphasized disciplined financial stewardship and alignment with shareholders while funding its immuno-inflammatory and rare disease strategy.

What regulatory progress did Vyome report for VT-1953 in Q1 2026?

Vyome submitted to the FDA an application for orphan drug designation for VT-1953 and proposals for next-stage development readiness. VT-1953 targets malignant fungating wounds, an area where the company notes there are currently no FDA-approved therapies specifically addressing the condition.

When will Vyome Holdings discuss its Q1 2026 results with investors?

Vyome plans a conference call and webcast on June 3, 2026, at 11:00 a.m. ET to discuss Q1 2026 results. Investors can join via webcast link or by dialing listed U.S./Canada and international numbers, with a replay available on the company’s website.

Filing Exhibits & Attachments

4 documents