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DOXANANO

DOXANANO develops Remotely Activated Chemotherapy (RAC®), a targeted drug delivery platform using proprietary DXN polymersomes. These nanocarriers encapsulate cytotoxic agents and release them precisely within the tumor microenvironment upon X-ray irradiation, minimizing systemic toxicity and enhancing therapeutic efficacy for solid tumors.

Traction –/10
Pessac, France · HQ
61K+ followers
Updated 5 months ago

Funding

Funding rounds are not available yet.

Founders

1 founder

Leslie Dubrana

Co-founder & Scientific Partnership Officer

Product

Problem

Conventional chemotherapy for solid tumors is limited by systemic toxicity, forcing dose reductions that compromise therapeutic efficacy. This necessitates a compromise between the maximum tolerated dose and the optimal anti-tumor dose, leading to suboptimal treatment outcomes and increased patient suffering.

Solution

DOXANANO is developing Remotely Activated Chemotherapy (RAC®), a targeted drug delivery platform utilizing proprietary DXN polymersomes. These nanocarriers safely encapsulate cytotoxic agents, protecting healthy tissues during systemic circulation. Upon external X-ray irradiation focused on the tumor site, the DXN polymersomes undergo a controlled cleavage, precisely releasing their therapeutic payload within the tumor microenvironment. This approach aims to enhance the concentration of chemotherapeutics at the tumor site while minimizing off-target exposure and associated adverse events. The platform's design allows for the encapsulation of both hydrophilic and hydrophobic agents, enabling combination therapies and offering a complementary modality to existing targeted therapies and immunotherapies.

Target Audience

The primary target audience includes oncologists, pharmaceutical companies, and clinical research organizations focused on solid tumor treatment.

Features

  • DXN polymersomes: Robust, spherical nanoparticles engineered from biocompatible and bio-sourced polymers.
  • Redox-sensitive polymer chemistry: Enables controlled cleavage and drug release triggered by X-ray irradiation.
  • Dual payload encapsulation: Capable of carrying both hydrophilic agents in the core and hydrophobic agents within the membrane.
  • Targeted release mechanism: X-ray-induced cleavage ensures precise spatio-temporal drug delivery within the tumor.
  • Versatile therapeutic application: Suitable for various cancer types, with initial focus on digestive and head and neck cancers.
  • Accelerated clinical pathway: Components (polymers, motifs, molecules) have prior regulatory approval for use in chemotherapy and radiotherapy.
  • Potential for imaging and targeting: DXNs can be tracked via non-invasive imaging and functionalized for biological targeting.
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