HINDNasdaqPharmaceutical PreparationsUS GAAP · USD

Vyome Holdings, Inc

Vyome Holdings, Inc. is a U.S.-based clinical-stage specialty pharmaceutical company organized around a biotechnology pipeline and a legacy pharmaceutical products business. Its development programs focus on immune-inflammatory and rare diseases, including topical and ophthalmic candidates, while the pharmaceutical segment includes antifungal products and related licensing arrangements.

Revenue0.3m USD
−96.0 %y/y
Operating profit (EBIT)-10.5m USD
−938.7 %y/y
EBIT margin-3,269.4%
−3,256.8 ppy/y
Net income-10.3m USD
−609.0 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-60-40-20020m USD2020: 1.6 m USD2020: EBIT -12 m USD20202021: 14 m USD2021: EBIT -58 m USD20212022: 11 m USD2022: EBIT -46 m USD20222023: 8.7 m USD2023: EBIT -15 m USD20232024: 8.0 m USD2024: EBIT -1.0 m USD20242025: 0.32 m USD2025: EBIT -10 m USD20250.32-10
RevenueOperating profit (EBIT)

Business

Share of revenue
Biotechnology pipeline0 %

Clinical and preclinical drug candidates for immune-inflammatory and rare diseases.

Pharmaceutical products100 %

Legacy antifungal products and related commercial pharmaceutical operations.

Licensing and collaboration rights0 %

Legacy licensing agreements and potential partnering arrangements around assets.

Products

Reported · share of revenue
54.6%36.6%8.8%FY2025100 %
  • Products54.6 %
  • License36.6 %
  • Royalty8.8 %

Source: 10-K FY2025, revenue the company reports per product line (SEC XBRL). Shares are of the lines shown and add up to 100 %.

Customers

The company’s biotechnology programs are aimed at patients with serious unmet medical needs, typically accessed through physicians, specialists, and clinical trial sites rather than direct consumer channels. Its pharmaceutical segment serves healthcare providers and patients through antifungal products, with commercialization shaped by licensing relationships and specialty prescribing patterns.

Specialty physicians and patients

They use the pipeline therapies for rare, inflammatory, or dermatologic conditions where current options are limited.

Healthcare providers

They prescribe the antifungal products and influence adoption through treatment protocols.

Clinical trial ecosystem

Investigators, sites, and enrolled patients support development of VT-1953, VT-1908, and VB-1953.

Licensing counterparties

Partners such as Sun Pharma-related arrangements support legacy pharmaceutical economics.

Strategy

The company’s strategy centers on advancing its lead clinical and preclinical programs toward regulatory milestones while preserving access to external capital. It also seeks to use collaborations, licensing, and financing tools to support development of its pipeline and legacy pharmaceutical assets.

Advance VT-1953 into pivotal developmentShort term

This is the lead program and the most advanced path to a potential commercial asset.

Progress the ophthalmology and acne pipelineMedium term

Diversifies the pipeline across multiple specialty indications and reduces single-asset dependence.

Secure external funding and partnershipsShort term

Clinical development requires capital and the company expects to rely on financing and collaborations.

Geography

Q2/2025

Vyome Holdings is based in the United States, with a reported operating footprint spanning Cambridge, Massachusetts, Princeton, New Jersey, and New Delhi, India. The U.S.-India structure matters because the company combines U.S.-based clinical and corporate functions with Indian innovation and development capabilities.

United States88 %
Europe6.5 %
Australia5.5 %
Other countries (US filing)0.1 %

Share of the revenue the company reports by geography.

Risks

Vyome’s business depends on successful clinical development, regulatory clearance, and the ability to finance a pipeline that has no approved biotechnology products. The company also faces execution risk from its dual-segment structure, where legacy pharmaceutical revenue is separate from development spending, and from the uncertainty of raising capital on acceptable terms.

Sorted by severity
Clinical development failure or delayHigh

Pipeline value depends on positive preclinical and clinical results and timely advancement.

ExposureVT-1953VT-1908VB-1953
Capital raising and liquidity riskHigh

The company expects to fund operations through equity, debt, and collaborations until product revenue exists.

Exposure: Corporate funding needs

Regulatory riskHigh

Drug development requires FDA alignment on protocols, approvals, and labeling.

Exposure: Pivotal trial and pre-IND programs

Commercialization risk in legacy pharmaMedium

Antifungal products and licensing arrangements may not generate enough scale to support the business.

Exposure: Pharmaceutical segment

Accounting

Judgemental items
Convertible promissory notes at fair value

The company elected fair value accounting, so changes in valuation can flow through earnings.

Impact: Non-cash income or expense volatility

Derivative accounting for embedded features

Embedded conversion or option features may need separate fair value measurement.

Impact: Can materially affect reported results period to period

Stock-based compensation

Employee and consultant awards are common in development-stage biotech and affect operating expense.

Impact: Dilution and expense recognition

Business combination and merger accounting

The merger and related recapitalization require careful purchase accounting and equity presentation.

Impact: Affects balance sheet and comparability

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026