Axorus (France)

French start-up developing a photoacoustic retinal prosthesis for AMD and other retinal degenerative diseases, based on technology licensed from Boston University (Chen Yang and Ji-Xin Cheng labs).

Key facts

  • HQ: Paris, France.
  • Founders / key stakeholders: Hélène Moulet (CEO / corresponding author on Leong 2026) and Jean-Damien Losasco (J-DL) — major stakeholders. Chen Yang and Ji-Xin Cheng (BU) — minor stakeholders. Yueming Li (BU) received partial Axorus research funding.
  • Technology: PDMS/candle-soot/PDMS flexible photoacoustic film. 1030-nm pulsed NIR laser converts each pixel of light into a localised ultrasound wave (~51 µm lateral resolution) that stimulates mechanosensitive retinal cells surviving in AMD/RP. Unlike retinal-prosthesis electrical prostheses, the mechanism is acoustic not electrical; unlike photovoltaic (PRIMA), stimulation is ultrasound not charge injection. See retinal-prosthesis for full modality comparison.
  • Product roadmap: developing a contact lens form factor that would project patterned NIR laser onto a subretinal PA film implant — no bulky external glasses required long-term (unlike PRIMA’s current headset). As of 2026 the technology is pre-clinical (rat subretinal implant results only).
  • Funding: NIH (via BU PIs) and Axorus SAS directly.
  • Stage (Aug 2026): Pre-clinical. Nature Communications paper published (Leong et al. 2026); next step is first-in-human safety study → clinical trial for blind patients. Chen Yang (BU) also plans a US start-up for domestic commercialisation.

Why it matters

The photoacoustic modality addresses a fundamental limitation of both electrical electrostimulation and photovoltaic prostheses:

  • Resolution: 51-µm acoustic pixel from a 50-µm fibre — better than PRIMA’s current 100-µm pixel and potentially scalable to sub-20 µm for meaningful acuity.
  • Coverage: the spatially continuous flexible film can in principle tile the full 25 mm² macula at up to 2,500 px/mm², whereas rigid photovoltaic chips are currently limited to 2×2 mm (7° visual field).
  • Mechanism: stimulates mechanosensitive cells (via Piezo channels and upstream glutamate pathways), which persist even after photoreceptor and bipolar-cell loss.
  • Safety: temperature rise <0.52 °C, MI <0.03–0.1, ISPTA <0.06–0.9 mW/cm² — all within FDA ophthalmic ultrasound guidelines.

Caveats / open questions

  • Results so far are rat-only (ex vivo and in vivo); best achieved acuity not yet measurable (SC activation is not the same as letter acuity).
  • Long-term biocompatibility not yet characterised (max 120 dpi for PDMS-CNT, 90 dpi for PDMS/CS/PDMS).
  • Mechanosensitivity structures not fully characterised; long-term adaptation unknown.
  • Surgery artefact (implant insertion track) needs refinement.
  • Acoustic waves are bidirectional — RPE/choroid effects require further investigation.
  • Patent portfolio for contact-lens form factor not publicly disclosed.
  • COI: study partially funded by and co-authored by Axorus stakeholders.

References

Footnotes

  1. raw/papers/leong-2026-photoacoustic-retinal-prosthesis.md

  2. raw/articles/bu-photoacoustic-retinal-prosthesis-2026.md