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.

Liikevaihto0,3milj. USD
−96,0 %v/v
Liikevoitto (EBIT)−10,5milj. USD
−938,7 %v/v
EBIT-marginaali−3 269,4%
−3 256,8 %-yks.v/v
Nettotulos−10,3milj. USD
−609,0 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−60−40−20020milj. USD2020: 1,6 milj. USD2020: EBIT −12 milj. USD20202021: 14 milj. USD2021: EBIT −58 milj. USD20212022: 11 milj. USD2022: EBIT −46 milj. USD20222023: 8,7 milj. USD2023: EBIT −15 milj. USD20232024: 8,0 milj. USD2024: EBIT −1,0 milj. USD20242025: 0,32 milj. USD2025: EBIT −10 milj. USD20250,32−10
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
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.

Tuotteet

Raportoitu · osuus liikevaihdosta
54,6%36,6%8,8%FY2025100 %
  • Products54,6 %
  • License36,6 %
  • Royalty8,8 %

Lähde: 10-K FY2025, yhtiön tuotelinjoittain raportoima liikevaihto (SEC XBRL). Osuudet on laskettu näytetyistä riveistä ja ne summautuvat 100 %:iin.

Asiakkaat

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.

Strategia

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 developmentLyhyt aikaväli

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

Progress the ophthalmology and acne pipelineKeskipitkä aikaväli

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

Secure external funding and partnershipsLyhyt aikaväli

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

Maantiede

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.

USA88 %
Europe6,5 %
Australia5,5 %
Other countries (US filing)0,1 %

Osuus liikevaihdosta, jonka yhtiö raportoi maantieteellisesti.

Riskit

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.

Järjestetty vakavuuden mukaan
Clinical development failure or delayKorkea

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

KohdistuuVT-1953VT-1908VB-1953
Capital raising and liquidity riskKorkea

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

Kohdistuu: Corporate funding needs

Regulatory riskKorkea

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

Kohdistuu: Pivotal trial and pre-IND programs

Commercialization risk in legacy pharmaKeskitaso

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

Kohdistuu: Pharmaceutical segment

Kirjanpito

Harkinnanvaraiset erät
Convertible promissory notes at fair value

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

Vaikutus: Non-cash income or expense volatility

Derivative accounting for embedded features

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

Vaikutus: 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.

Vaikutus: Dilution and expense recognition

Business combination and merger accounting

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

Vaikutus: Affects balance sheet and comparability

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 24.9.2026