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SA-VOIR SIGNED

Assessing the feasibility of MT-011, a first-in-class drug to treat glaucoma and other neurodegenerative diseases via a breakthrough mechanism-of-action

Total Cost €

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EC-Contrib. €

0

Partnership

0

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 SA-VOIR project word cloud

Explore the words cloud of the SA-VOIR project. It provides you a very rough idea of what is the project "SA-VOIR" about.

011    business    followed    small    broad    parkinson    molecule    start    newly    30    inhibiting    deal    deterioration    applicable    assay    biotechnological    nanomolar    black    implicated    form    family    inhibits    causes    patients    licensing    manner    size    40m    total    world    aside    guide    upfront    de    inherently    attract    applicability    assets    drugs    companies    seeing    indicated    neurodegenerative    proprietary    pharmaceuticals    imminent    hyperactivated    house    enzyme    peripheral    strengthen    receive    million    prominent    people    plan    irreverisble    commercialize    act    tension    drug    glaucoma    santen    alzheimer    clinical    investment    eye    components    elucidated    candidate    trials    dysregulation    report    optimization    payments    pharmaceutical    neurogenerative    risked    diagnosed    documents    voir    milestone    vision    diseases    tunnel    halt    vash    disorder    affinity    subtype    sa    normal    continued    mt    blindness    outline    critical    pfizer    stage    biochemical    inhibit    treatments   

Project "SA-VOIR" data sheet

The following table provides information about the project.

Coordinator
MT ACT 

Organization address
address: 66 RUE DU CLAOUS
city: CAZILHAC
postcode: 34190
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country France [FR]
 Total cost 71˙429 €
 EC max contribution 50˙000 € (70%)
 Programme 1. H2020-EU.3. (PRIORITY 'Societal challenges)
2. H2020-EU.2.3. (INDUSTRIAL LEADERSHIP - Innovation In SMEs)
3. H2020-EU.2.1. (INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies)
 Code Call H2020-SMEInst-2018-2020-1
 Funding Scheme SME-1
 Starting year 2019
 Duration (year-month-day) from 2019-12-01   to  2020-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MT ACT FR (CAZILHAC) coordinator 50˙000.00

Map

 Project objective

Glaucoma is the world's leading cause of irreverisble blindness, affecting 20 million people in Europe and the US. Known as the Alzheimer’s of the eye, glaucoma is a neurodegenerative disorder that causes deterioration in peripheral vision. Affected patients report ‘seeing through a black tunnel’. Treatments to halt vision loss are available however, they are only applicable for the ‘high tension glaucoma’ subtype. For those diagnosed with ‘normal tension', which comprises over 30% of glaucoma patients, no treatments are available, and vision loss is imminent. New drugs that inhibit VASH, a newly elucidated enzyme that is hyperactivated in many neurogenerative diseases, have potential to address this need.

We at MT-act are a biotechnological start-up who have identified a family of VASH-inhibiting small molecule drugs. Using an in-house proprietary biochemical assay followed by lead optimization, we have identified MT-011, which inhibits VASH with nanomolar affinity, as our lead candidate. Aside from glaucoma, VASH dysregulation is also implicated in other prominent neurodegenerative diseases such as Alzheimer’s and Parkinson’s. Our assets therefore have an inherently broad applicability.

We aim to develop MT-011 up to the stage of Phase 1 clinical trials, upon which we aim to commercialize the drug via a licensing deal with a pharmaceutical partner. We will then receive upfront and milestone payments with a estimated total deal size of €40M. We are currently in discussion with world-leading pharmaceutical companies Pfizer and Santen Pharmaceuticals, who have already indicated interest in our drugs.

In SA-VOIR, we aim to strengthen the business case for MT-011 and to outline a detailed technical plan for its continued development. These documents will not only guide us in developing MT-011 towards Phase 1 trials in an effective and de-risked manner, it will also form critical components of a business plan that we will use to attract further investment.

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The information about "SA-VOIR" are provided by the European Opendata Portal: CORDIS opendata.

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