TBM (Applied Biomedical Research with a Primary Social finality) projects

Objective

In the long term, the TBM programme aims at contributing to the implementation of (new) therapies, diagnostic techniques and preventive methods, which, without government funding, would not make it to the patient due to a lack of industrial interest.

Features

  • Project period: 2 to 4 years
  • Start of project: October 1, 2018
  • Eligible organisations: research centres (e.g. universities, university hospitals, university colleges (‘hogescholen’) and strategic research centres)
    • max. 20% of the budget is earmarked for non-Flemish research centres
    • at least 10% of the budget should be earmarked for applicants that are a Flemish hospital or ITM (because of the clinical finality)
  • Acceptable costs:
    • staffing, operation, equipment, subcontracting contracts (in accordance with cost model rules)
    • max. 1,000,000 euro (for large or multicentric trials, exceptionally budgets up to 1,500,000 euro are allowed)
    • min. 250,000 euro
  • Funding percentage: 100%
  • Available budget for the current call: 14,000,000 euro
  • Call open: from December 1, 2017
  • Submission of project proposals via the FWO e-portal
  • Call closed
  • Announcement of results: July 2018
  • Success rate 2017: 31%

Profile and conditions

  • Your project satisfies each of the following 4 conditions:
  1. It is aimed at the development of a new therapy, diagnosis and/or specific prevention of a particular human disease/medical issue or a comparison of existing therapies, diagnostics or preventive methods in order to find out their relative efficacy and cost-effectiveness.
  2. It is directed at research that is positioned late in the path from discovery to a specific application (i.e. there is a clinically relevant proof-of-concept) and aims at translating and developing scientific findings into clinical applications rather than creating new knowledge from scratch. On the other hand, it is not positioned too late in the path from discovery to application: it does not consist of implementation activities that no longer require any research.
  3. It offers a clear applicability with an added value for the Flemish health situation, including at least a positive medical impact for a particular group of patients or a cost reduction for the Flemish healthcare system.
  4. At the time of submitting the application (or in the near future), the industry is not interested in your project for commercial reasons.
  • For the execution of the project, you need bench fees, equipment and personnel grants.
  • The organisation(s) to which you belong, is a (are) research centre(s).
  • The project executors are the owners of their own results.

Important changes compared to the previous call

  • From this call onwards, FWO requires that clinical trials are registered in a suitable clinical trial database (e.g. clinicaltrials.gov) before the start of the trial. When the first patient is included in the trial, you should inform FWO (via tbm@fwo.be) about the start date of the trial (first patient in) and the registry number of the clinical trial.
  • FWO has made data management a key element of its policy. It covers procedures on the description of research data and metadata, their storage and long-term preservation, the discoverability, the designation of responsible persons, the handling of highly sensitive data, and the open access to and sharing of research data. From this call onwards, the application form in the FWO e-portal contains several issues that need to be addressed concerning data management. Furthermore, if a proposal receives funding, a data management plan will be requested.

Procedure

  • If you have doubts as to whether your idea may or may not fit within the TBM programme objectives, you can obtain FWO’s opinion by providing a short abstract (1-2 pages), sent via e-mail to tbm@fwo.be. It is also possible to request an oral preliminary discussion at FWO; please attach a short abstract, as well as any questions that you would like to see answered.
  • As supervisor of the project, you prepare your proposal via the FWO e-portal and submit your (complete) proposal to your host institution (=main applicant of the proposal) by March 16, 2018 at 5 PM.
  • Your host institution submits your proposal to FWO via the e-portal by March 23, 2018 at 5 PM.
  • Your proposal is reviewed by a number of (inter)national experts who will discuss and evaluate your proposal during a panel meeting at FWO. During the expert panel meeting you have the opportunity to briefly interact with the experts (to provide answers to the most crucial questions of the experts). The panel meetings will probably take place on one of the following dates: June 4, June 7, June 11, June 15, 2018. You will be informed about the exact date of your panel meeting as soon as possible.
  • The expert panels report to the board of directors of FWO.
  • The board of directors decides on granting support.
  • Subsequently, you will receive feedback on the decision.

Regulations and downloads

Contact

For questions with regard to the modalities of the TBM programme, please contact tbm@fwo.be. Questions regarding the functionality of the e-portal, should be addressed to fwohelpdesk@fwo.be.