DTILNasdaqBiological Products, (No Diagnostic Substances)US GAAP · USD

Precision BioSciences, Inc

Precision BioSciences is a U.S.-based clinical-stage gene editing company built around its proprietary ARCUS genome editing platform. The company develops in vivo therapies for genetic and infectious diseases and also licenses ARCUS-related intellectual property to collaborators and other biotechnology companies.

Liikevaihto34,3milj. USD
−50,1 %v/v
Liikevoitto (EBIT)−52,1milj. USD
−99,3 %v/v
EBIT-marginaali−152,2%
−114,1 %-yks.v/v
Nettotulos−45,7milj. USD
−738,0 %v/v
Vapaa kassavirta−65,9milj. USD
−12,3 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−150−100−50050100150milj. USD2020: 24 milj. USD2020: EBIT −110 milj. USD20202021: 116 milj. USD2021: EBIT −39 milj. USD20212022: 25 milj. USD2022: EBIT −62 milj. USD20222023: 49 milj. USD2023: EBIT −44 milj. USD20232024: 69 milj. USD2024: EBIT −26 milj. USD20242025: 34 milj. USD2025: EBIT −52 milj. USD202534−52
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
ARCUS platform and therapeutic programs85 %

Development of proprietary genome editing tools and therapeutic candidates for human disease.

Licensing and collaboration revenue15 %

Upfront payments, milestones, and royalties from partners using ARCUS-related IP.

Asiakkaat

Precision BioSciences sells primarily to pharmaceutical and biotechnology partners through licensing and collaboration agreements, while its internal programs are aimed at future patients with genetic or infectious diseases. Its commercial counterparties are research-driven companies that need access to genome-editing IP, preclinical know-how, or therapeutic development rights. If approved, future products would be used by hospitals, specialists, and treatment centers rather than sold directly to consumers.

Biotechnology and pharmaceutical collaborators

License ARCUS IP or partner on preclinical programs in exchange for upfront fees, milestones, and royalties.

Future therapeutic end users

Patients with genetic or infectious diseases who would receive approved ARCUS-based therapies.

Research and development partners

Companies and institutions that use ARCUS in discovery, preclinical, or translational work.

Strategia

The company’s strategy is to advance ARCUS-based in vivo therapies while using partnerships and licensing to monetize its platform before full product commercialization. It also seeks to expand its intellectual property portfolio and manufacturing know-how so it can support future clinical and commercial development. These priorities are intended to preserve optionality across both internal drug development and external licensing.

Advance ARCUS therapeutic pipelineKeskipitkä aikaväli

Internal programs are the main path to long-term value creation and future product revenue.

Monetize platform through licensing and collaborationsLyhyt aikaväli

Partner deals can generate non-product revenue and external validation of ARCUS technology.

Strengthen IP and development capabilitiesKeskipitkä aikaväli

Genome editing is highly IP-intensive and requires strong preclinical and manufacturing execution.

Maantiede

Precision BioSciences is headquartered in the United States and conducts its research, development, and corporate activities from there. Its collaboration and licensing model can reach global partners, but the company’s operating footprint is centered on U.S.-based scientific and regulatory infrastructure. Because its programs are pre-commercial, geography matters mainly through where trials, partners, and regulatory approvals are pursued.

Riskit

Precision BioSciences faces the typical risks of a clinical-stage gene editing company: uncertain clinical outcomes, regulatory approval risk, and heavy dependence on intellectual property protection. Its business also depends on third-party collaborators, contract research and manufacturing providers, and future access to capital, which can all affect timing and execution. As a pre-commercial company, it is also exposed to cybersecurity, patent, and biosimilar competition risks if any products are approved.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical development failure1Financing risk2Regulatory approval risk3Intellectual property and license risk4Partner concentration and collaboration risk5Cybersecurity and third-party execution risk6
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical development failureVaikutus: KorkeaTodennäköisyys: Korkea

    Therapeutic candidates are still in development and may not show safety or efficacy.

    Kohdistuu: In vivo gene editing programs

  2. Financing riskVaikutus: KorkeaTodennäköisyys: Korkea

    The company has not generated product sales and relies on external capital to fund R&D.

    KohdistuuEquityDebtCollaboration financing
  3. Regulatory approval riskVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Gene editing products face stringent FDA and foreign review, with possible restrictions or denial.

    Kohdistuu: Future BLA or foreign marketing applications

  4. Intellectual property and license riskVaikutus: KorkeaTodennäköisyys: Kohtalainen

    The business depends on patents and license agreements that can expire or be challenged.

    Kohdistuu: ARCUS platform and Cellectis-related license terms

  5. Partner concentration and collaboration riskVaikutus: KeskitasoTodennäköisyys: Korkea

    A meaningful part of revenue comes from collaboration accounting and partner milestones.

    KohdistuuNovartisCaribouTG TherapeuticsImugene
  6. Cybersecurity and third-party execution riskVaikutus: KeskitasoTodennäköisyys: Matala

    R&D, manufacturing, and collaborator data flows depend on external systems and vendors.

    KohdistuuCROsCMOsCollaboratorsInternal systems

Kirjanpito

Harkinnanvaraiset erät
Revenue recognition for collaboration and license agreements

Revenue depends on performance obligations, deferred revenue release, and milestone events.

Vaikutus: Can cause large fluctuations unrelated to current-period cash receipts

Deferred revenue roll-off

Prior upfront payments are recognized over time or at contract completion.

Vaikutus: Major driver of year-to-year revenue variability

Stock-based compensation

A meaningful non-cash expense for a small, research-intensive biotech company.

Vaikutus: Affects operating loss and comparability across periods

Lease accounting and R&D commitments

The company uses leased facilities and third-party research/manufacturing services.

Vaikutus: Affects balance sheet liabilities and operating expense timing

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 24.9.2026