Pixium Vision (PIX)

Business description

Pixium Vision develops bionic retinal implants for patients with severe vision loss. A wireless sub-retinal implant (Prima), designed for Dry-ARMD patients, is in a human feasibility study in Europe and is expected to start a US feasibility study in Q218.

Stock data

Market cap.€40.9m
Last close€3.10
High / Low (52 weeks)€7.3 / €2.5
Stock market listingEU
Forecast net debt (€m)1.8
Forecast gearing ratio (%)16
TeamHealthcare
SectorPharmaceutical & healthcare

Price performance

%1m3m12m
Actual3.3(0.2)(52.8)
Relative *7.60.3(56.7)

* % Relative to local index

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Company news

BRIEF-Pixium Vision Gets FDA Approval For Human Clinical Study Of Prima Sub ...

Thu, 04 Jan 2018 06:00:00 GMT

Pixium Vision receives FDA approval to begin human clinical study of its PRIMA ...

Thu, 04 Jan 2018 06:00:00 GMT

Pixium Vision announces CE market approval of IRIS

Mon, 25 Jul 2016 04:52:30 GMT

Pixium Vision Receives Approval for First-in-Human Clinical Trial of PRIMA ...

Thu, 19 Oct 2017 04:52:30 GMT

Pixium Vision Announces Updates on Its Epi-retinal IRIS

Wed, 27 Sep 2017 04:52:30 GMT

Y/E Dec Revenue (€m) EBITDA (€m) PBT (€m) EPS (c) P/E (x) P/CF (x)
2015A 3.3 (14.6) (15.6) (122.88) N/A N/A
2016A 2.5 (11.4) (12.4) (97.60) N/A N/A
2017E 2.8 (11.5) (13.3) (101.00) N/A N/A
2018E 3.0 (14.6) (18.8) (138.68) N/A N/A

Last updated on 13/12/2017

Investment summary

Pixium announced on 25 January 2018 the first human activation of the Prima wireless photovoltaic sub-retinal implant, following successful implantation one month ago. These events occurred as per the protocol of the five-patient European Prima feasibility study, which was approved by regulators in October 2017 to assess the device in patients who have lost light perception in their central visual field due to atrophic damage from atrophic dry age-related macular degeneration. Following Prima activation, the patient reported light perception in the central visual field, where there had been none previously, and will now proceed to visual re-training, to learn how to interpret the elicited light signals emitted by the Prima system. The successful Prima activation in this first patient is encouraging as an early suggestion of proof-of-concept that the device can interface with retinal cells to restore some visual perception. Additional implantations, along with results from the six-month safety assessment in this study, may further validate the Prima approach and potential.

Last updated on 30/01/2018

Industry outlook

Second Sight (EYES) is commercialising an epiretinal implant (Argus II) in the US and EU approved for Retinitis Pigmentosa. PRIMA has been designed and being evaluated in clinical studies as a potential treatment option initially for dry-AMD, a common disease in aging population and a significant unmet medical need.

Last updated on 13/12/2017

Key management

Khalid Ishaque, CEO
Didier Laurens , CFO

Company address

74 rue du Faubourg Saint-Antoine
Paris
75012
United Kingdom
+33 1 76 21 47 30
View website