SIGNIA: An innovative drug discovery platform for rapid identification and validation of antimicrobial applications in available pharmaceutical resources and drugs open for repurposing.

Project Information

SIGNIA

Grant agreement ID: 826722

DOI

10.3030/826722

Project closed

EC signature date 16 July 2018

Start date 1 August 2018

End date 30 November 2018

Funded under

• INDUSTRIAL LEADERSHIP - Innovation In SMEs

Total cost

€ 71 429,00

EU contribution

€ 50 000,00

Coordinated by

SIGNIA THERAPEUTICS
France

Periodic Reporting for period 1 - SIGNIA (SIGNIA: An innovative drug discovery platform for rapid identification and validation of antimicrobial applications in available pharmaceutical resources and drugs open for repurposing.)

Reporting period: 2018-08-01 to 2018-11-30

Summary of the context and overall objectives of the project

The Final Report resumes the work done by Signia during Phase 1 execution in order to verify the feasibility of Signia project to optimize our disruptive drug repurposing platform and release it to the market. We planned to improve its screening capability and to in-house develop customized nebulization devices, to later undergo clinical validation. We made an assessment of all the investment required to complete the project, for which we will pursue financing support of circa €2.5M from the EC scheme of SMEi Phase 2. After an assessment of Signia´s financial analysis, we have evaluated the potential of Signia to generate profit (€31.6M of revenue and €22.5M profit) and new employment (+14 new job positions). We have already received positive proofs of interest from our key stakeholders: public research centres (Centre Hospitalier Universitaire de Québec, Centre d´Etude des Pathologies Respiratoires INSERM UMR 1100 at Université de Tours or Lille University Hospital) and private pharma and biotech companies (Sanofi, Cynbiose or Evotec).
Finally, we concluded to continue with Signia project, motivated by our feasibility study which confirms the uniqueness and competitiveness of our innovation.

Work performed from the beginning of the project to the end of the period covered by the report and main results achieved so far

TECHNICAL FEASIBILITY, including: product specification and technology definition; analysis of validation procedures; detailed technical plan to increase TRL to 9; analysis of risks and design of a mitigation and contingency plan.
COMMERCIAL FEASIBILITY, including: market analysis; end-user´s segmentation; main competitors; definition of commercial strategy; SoA and FtO analysis; business model; commercialization and dissemination plan, including IPR strategy.
FINANCIAL FEASIBILITY, including: in-depth cost analysis to evaluate our capacity to take the innovation; business projections for the first five years after Signia market launch in a conservative sales scenario.

Progress beyond the state of the art and expected potential impact (including the socio-economic impact and the wider societal implications of the project so far)

Signia will be the first drug discovery platform to identify new antimicrobial application among available drugs and pharmaceutical resources, avoiding the impact of intrinsic microbe mutability by targeting the infected cell, making possible to identify a broad spectrum of antimicrobials by targeting common features of an infected cell, and accelerating drug discovery process in terms of cost, regulations and time-to-market. It will allow a huge growth for our company (+€31.6M revenue and +14 new employees at the 4th year of commercialization).

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