Asset Manager

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Nanobiotix

Laurent Levy and colleagues founded Nanobiotix in Paris in 2003 to build a company around a physical mechanism that had not been applied systematically to...

Nanobiotix

Laurent Levy and colleagues founded Nanobiotix in Paris in 2003 to build a company around a physical mechanism that had not been applied systematically to oncology—elevating radiation dose within cancer cells without raising toxicity in surrounding tissue. The firm spent its first decade on preclinical and early clinical work, gradually collecting data showing that its inert hafnium oxide nanoparticles, injected directly into a tumor, absorb ionizing radiation and re-emit it as a cloud of electrons that tear apart cancer cell DNA. The company listed on Euronext in 2012 and later secured a secondary listing on Nasdaq. The firm's strategy has centered on establishing NBTXR3 as a universal radioenhancer, not a single-indication drug. Trials span soft tissue sarcoma—which earned a CE mark in 2019 allowing European commercialization—head and neck cancers, lung, esophageal, pancreatic, and other solid tumors where radiotherapy is standard of care. The company places equal weight on immunotherapeutic combinations, testing whether radiation-amplified cell death produces an abscopal effect that primes tumors for checkpoint inhibitors. In 2019, Nanobiotix signed a global licensing agreement with Janssen Pharmaceuticals for NBTXR3 across multiple solid-tumor indications outside Asia (per Nanobiotix, 2019). The collaboration expanded in 2023 with a $25 million upfront payment and a $43 million equity investment from Johnson & Johnson Innovation, alongside an amended co-development framework (per company communications, July 2023). A concurrent joint strategic collaboration with The University of Texas MD Anderson Cancer Center, announced September 2023, covers a multi-arm clinical development program spanning several tumor types. Nanobiotix maintains its headquarters in Paris and a US office in Cambridge, Massachusetts. The company reports headcount on a consolidated basis in its annual filings; while current team size is not independently confirmed, historically its operations have been sized for a single-product, capital-efficient development model. The firm has not disclosed an in-house investment vehicle or family-office structure, functioning instead as a public biotech whose capital allocation is governed by a board and executive management. The MD Anderson and J&J agreements, reached within weeks of each other in 2023, constituted the most operationally significant period in the company's history since the original CE mark, setting up NBTXR3 for simultaneous exploration across multiple organ sites. The firm's structural differentiator is its asset being a physical device rather than a biologic or small molecule. Because NBTXR3 does not interact chemically with any cellular pathway, its safety profile depends on injection precision rather than systemic toxicity, and it is likely to resist the tumor-mutation escape that complicates targeted therapies. That physics-based universality allows Nanobiotix to advance one product through dozens of registrational trials and partnerships without the typical pharmaceutical need to build a molecule-by-molecule pipeline.

General information

Firm type

Asset Manager

Year founded

2003

AUM

Undisclosed

Location

Region

Europe

Country

France

City

Paris

Corporate office

Paris, France

Additional offices

Cambridge, Massachusetts, United States

Principals

Laurent Levy

Co-Founder, Chief Executive Officer, and Chairman

Sector focus

Digital HealthOncology

Frequently asked questions

Who runs investment and strategic decisions at Nanobiotix?

Co-Founder Laurent Levy serves as CEO and Chairman, so he ultimately directs capital allocation and partnership strategy. As a publicly listed company on Euronext and Nasdaq, major investment decisions are subject to board oversight and, for large partnering and financing events, shareholder votes. The executive team includes a CFO and a Chief Medical Officer, with investor relations managed from the Paris headquarters.

What does Nanobiotix actually own—is it a fund, a biotech, or something else?

Nanobiotix is a clinical-stage biotechnology company, not a fund or family office. It owns proprietary intellectual property around hafnium oxide nanoparticles—branded as NBTXR3—and a portfolio of clinical data and regulatory filings. It generates no revenue from asset management; its business is developing NBTXR3 toward regulatory approvals and commercialization, funded through equity raises, licensing fees, and partnership milestones.

Does Nanobiotix make direct investments or participate in fund structures?

No. Nanobiotix does not operate an investment arm or a venture fund. It invests capital raised from public markets and corporate partners exclusively into its own clinical development programs, manufacturing scale-up, and research collaborations related to NBTXR3.

How does Nanobiotix's relationship with Johnson & Johnson work?

In 2019, Nanobiotix signed a global exclusive licensing agreement with Janssen Pharmaceuticals—a Johnson & Johnson company—covering NBTXR3 outside Asia (per Nanobiotix, 2019). In July 2023, that relationship deepened when Johnson & Johnson Innovation made a $25 million upfront payment and a $43 million equity investment while the companies amended their co-development terms (per company communications, July 2023). Janssen runs substantial portions of the clinical development program under this agreement.

What is the company's geographic focus?

Nanobiotix is headquartered in Paris and maintains a US office in Cambridge, Massachusetts. Its clinical trials span Europe, the United States, and Asia, with the Asia-region rights for NBTXR3 held by a separate partner, LianBio, under a licensing agreement. The company's European CE mark approval enables commercialization in the EU soft tissue sarcoma market.

Which indications does Nanobiotix explicitly target or avoid?

The company explicitly targets solid tumors treated with radiotherapy—soft tissue sarcoma, head and neck squamous cell carcinoma, non-small cell lung cancer, pancreatic cancer, esophageal cancer, and others. It does not target hematologic malignancies, which are not treated with injectable-localized radiotherapy, reflecting the physical-mechanism constraint of the product.

What is the regulatory status of NBTXR3?

NBTXR3 received CE mark approval in Europe in April 2019 for locally advanced soft tissue sarcoma (per Nanobiotix disclosure, 2019). In the United States, it remains an investigational product under active FDA study, including a Phase 3 trial in head and neck cancer. It does not yet hold FDA marketing authorization for any indication.

Profile maintained by using OSINT (open-source intelligence), regulatory filings, licensed data partners, and verified direct submissions. Read the methodology. Last updated: . Continuous refresh with full update cycles at least every 30 days.

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