RANINasdaqPharmaceutical PreparationsUS GAAP · USD

Rani Therapeutics Holdings, Inc.

Rani Therapeutics Holdings, Inc. is a U.S.-based clinical-stage biotherapeutics company developing oral delivery technology for biologics and other drugs. Its core platform, the RaniPill capsule, is designed to deliver drug substances such as antibodies, proteins, peptides, and oligonucleotides through the gastrointestinal tract, with development activities centered in the United States and intended for global use.

Liikevaihto1,6milj. USD
+58,9 %v/v
Liikevoitto (EBIT)−38,3milj. USD
+28,1 %v/v
EBIT-marginaali−2 346,0%
+2 840,2 %-yks.v/v
Nettotulos−29,7milj. USD
+1,1 %v/v
Vapaa kassavirta−18,8milj. USD
+47,4 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−80−60−40−20020milj. USD2020: 0,46 milj. USD2020: EBIT −17 milj. USD20202021: 2,7 milj. USD2021: EBIT −52 milj. USD20212022: 0,00 milj. USD2022: EBIT −63 milj. USD20222023: 0,00 milj. USD2023: EBIT −66 milj. USD20232024: 1,0 milj. USD2024: EBIT −53 milj. USD20242025: 1,6 milj. USD2025: EBIT −38 milj. USD20251,6−38
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
RaniPill GO20 %

Microtablet-based oral capsule designed to deliver small biologic doses with high bioavailability.

RaniPill HC20 %

High-capacity capsule under development for liquid payload delivery of larger biologics.

Partnered development and evaluation services60 %

Technology evaluation, transfer, and collaboration work performed for third-party biopharma partners.

Asiakkaat

Rani’s customers are primarily biopharmaceutical companies that want to convert injectable biologics into oral therapies using its delivery platform. The company also serves potential development partners seeking evaluation, technology transfer, and collaboration around specific compounds and drug targets. End users of the technology are patients and healthcare systems, but the direct commercial customer is typically the drug developer or license partner.

Biopharmaceutical collaboration partners

Companies that license or co-develop the RaniPill platform for specific biologic or drug programs.

Technology evaluation customers

Partners that pay for evaluation services to assess whether their compounds can be delivered orally.

Future commercial pharma customers

Drug developers that may adopt the platform for approved products if clinical and regulatory milestones are met.

Strategia

Rani’s strategy is to advance the RaniPill platform through clinical development while partnering with biopharma companies that want oral delivery for their biologics. A second priority is building manufacturing capability for the capsule and related device components so the platform can scale if programs succeed. The company also seeks collaboration structures that can fund development and create milestone and royalty economics.

Advance clinical validation of the RaniPill platformLyhyt aikaväli

Human data is needed to prove oral delivery performance and support regulatory progress.

Secure and expand biopharma collaborationsLyhyt aikaväli

Partner programs can create non-dilutive funding and validate the platform with named drug developers.

Scale manufacturing and device productionKeskipitkä aikaväli

Commercial adoption will require reliable capsule manufacturing and supply chain control.

Maantiede

Rani is headquartered in the United States and conducts its development, engineering, and manufacturing activities primarily there. The company has indicated that future commercialization, if achieved, could extend to the United States, Europe, Asia, and other key markets through its own infrastructure or partners. Geography matters because the platform is intended for global pharmaceutical use, while regulatory approval and partner execution will determine where revenue is ultimately realized.

Riskit

Rani faces the typical risks of a clinical-stage biotechnology company: uncertain clinical outcomes, regulatory approval risk, and dependence on third-party partners and suppliers. Its business model also requires substantial capital before any commercial product revenue, so financing access and Nasdaq listing compliance are material to execution. Because the platform is still being developed, manufacturing scale-up, intellectual property protection, and partner commitment are all important sources of risk.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical and regulatory failure1Lack of commercial product revenue2Financing and dilution risk3Partner concentration and collaboration dependence4Supply chain and manufacturing execution5Nasdaq listing compliance6
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical and regulatory failureVaikutus: KriittinenTodennäköisyys: Korkea

    The RaniPill platform must prove safety, bioavailability, and efficacy across programs.

    Kohdistuu: RaniPill GO and RaniPill HC

  2. Lack of commercial product revenueVaikutus: KorkeaTodennäköisyys: Korkea

    The company is still in development, so revenue depends on future approvals and partner execution.

    Kohdistuu: Platform-wide

  3. Financing and dilution riskVaikutus: KorkeaTodennäköisyys: Korkea

    Development and manufacturing require capital before product sales are available.

    Kohdistuu: Corporate funding

  4. Partner concentration and collaboration dependenceVaikutus: KorkeaTodennäköisyys: Kohtalainen

    A major portion of future economics may depend on one or a few collaboration agreements.

    Kohdistuu: Chugai collaboration

  5. Supply chain and manufacturing executionVaikutus: KeskitasoTodennäköisyys: Korkea

    The platform relies on third-party APIs/components and complex device manufacturing.

    KohdistuuSingle-source suppliersAutomated lines
  6. Nasdaq listing complianceVaikutus: KeskitasoTodennäköisyys: Korkea

    Failure to maintain listing standards could reduce liquidity and investor access.

    Kohdistuu: Public equity market access

Kysy Clarifolta: Rani Therapeutics Holdings, Inc.

Kirjanpito

Harkinnanvaraiset erät
Contract revenue recognition

Evaluation services for partners like Chugai are recognized as services are delivered, affecting quarter-to-quarter revenue.

Vaikutus: Small but important for collaboration economics

R&D expense classification

Clinical work, engineering, materials, and stock compensation drive reported operating loss.

Vaikutus: Primary driver of period expenses

Capitalization of manufacturing assets

Assets with alternative future use may be capitalized, while other project costs are expensed.

Vaikutus: Affects balance sheet size and near-term earnings

Non-controlling interest accounting

Loss attribution between Rani and non-controlling interests changes reported net loss attributable to shareholders.

Vaikutus: Impacts earnings attribution

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 24.9.2026

Rani Therapeutics Holdings, Inc. (RANI) liikevaihto, tulos ja tunnusluvut 2025 – Clarifo