agentschap voor Innovatie door Wetenschap en Technologie agentschap voor Innovatie door Wetenschap en Technologie Transformational Medical Research Transformationeel Geneeskundig Onderzoek TGO 13 april 2015 Katrien Swerts Transformational Medical Research - TGO Context Transformational Medical Research – TGO Key features TGO programme Technicalities Questions 3 Context TGO-programme Recently, a remarkable progress has been made in the field of medical basic research. New discoveries do not always result in new, effective medicines. 4 Context TGO-programme The classical drug development path (clinical phase I, II and III studies) may form an obstacle for the development of innovative therapeutics. 0 1 Hit ID 3 Lead optimization 3.5 Candidate stage 5 NME 7 Phase I 9 Phase II 12 Phase III Long and expensive drug development process 5 Context TGO-programme The classical drug development path (clinical phase I, II and III studies) may form an obstacle for the development of innovative therapeutics. Low success rate 6 Context TGO-programme Consequences: Patients need to wait for quite a long time before new, sometimes lifesaving drugs reach the market. New drugs are quite expensive. Increasing health care expenditures in Flanders, Belgium, Europe,… Context TGO-programme We need to reform the drug development process in order to speed up the development of innovative, more effective drugs. Bridge the ‘innovation gap’ Redesign clinical trials Implement biomakers in order to identify specific target populations Increase the cost effectiveness of the process … 8 Transformational Medical Research programme The Flemish government (Min Ingrid Lieten) decided to step in and launch the Transformational Medical Research (TGO) programme: Accelerate development of more effective, safe and affordable drugs Strengthen the Flemish biopharma cluster Make Flanders an attractive region for innovative clinical trials Provide our society with access to the best therapies … 9 Transformational Medical Research programme The Flemish government (Min Ingrid Lieten) decided to step in and launch the Transformational Medical Research (TGO) programme: Budget Call 2012-2013: 10 million EUR. Call will be organised by IWT. 10 Key features TGO-programme Key features of TGO-programme: Support relevant collaborations between companies, research organizations and clinical centres Focus on adaptive clinical research projects with an economic and social added value A substantial contribution to the current state of the art is mandatory Use of biomarkers and/or biological samples from biobanks is encouraged. Key features TGO-programme Key features of TGO-programme: Support relevant collaborations between companies, research organizations and clinical centres 12 Key features TGO-programme Consortium: Companies, research organisations and clinical centres. Consortium consists of at least one company and one research organisation. 13 Key features TGO-programme Consortium: Companies, research organisations and clinical centres. Consortium consists of at least one company and one research organisation. Balanced consortium 14 Key features TGO-programme Key features of TGO-programme: Focus on adaptive clinical research trials with an economic and social added value TGO projects have a double finality Important feature compared to other IWT programmes (e.g. R&D, SBO-E versus SBO-M, TBM) Reach a relevant social goal, bringing in industrial expertise 15 Key features TGO-programme Key features of TGO-programme: Focus on adaptive clinical research trials with an economic and social added value Substantial valorisation potential Economic valorisation in Flanders Investments / Employment Large utilisation of project results Impact on the Flemish health care situation Positive medical impact on a specific patient population 16 Key features TGO-programme Adaptive clinical trials: A clinical trial design that uses accumulating data to decide on how to modify aspects of the study as it continues, without undermining the validity and integrity of the trial. (Gallo et al., 2006) Size of cohort Clinical end points Dose Response criteria Inclusion criteria … 17 Key features TGO-programme Adaptive clinical trials: 18 Key features TGO-programme Key features of TGO-programme: A substantial contribution to the current state of the art is mandatory Knowledge creation is essential! Clinical Phase III trials without inventive approach or clinical trials, focused on registration will not be funded. 19 Technicalities TGO-programme Integration The modules should form an integrated project. Additionality Consortium approach should have an added value compared to individual R&D, SBO or TBM projects. 20 Technicalities TGO-programme Intellectual property Company Module 1 Research and Development Research organisation Clinical centre Owner project results Subcontractor: Market price or cost + margin No IP rights Research partner: Actual cost Participate in generated IP (Agreements should not hinder industrial valorisation) Technicalities TGO-programme Owner project results Module 2 Strategic Basic Research Research organisation Clinical centre Transfer of results to companies / spin-off: Market conform transfer Consortium partners do not have preferential access to the results. Interested companies may have a ‘right of first negotiation’. Revenues should be reinvested in R&D. Transfer of results to social actors Subcontractors: no IP rights Technicalities TGO-programme Intellectual property Owner project results Module 3 Applied Research Research organisation Clinical centre No transfer of results to companies / spin-offs. Industry is not interested in the project results Subcontractors: no IP rights Technicalities TGO-programme Budget Total project budget Budget Module 1 Research and Development Budget Company 1 Budget Module 2 Strategic Basic Research Budget Company 2 Budget Research partner Budget Module 3 Applied Research Technicalities TGO-programme Budget IWT cost model: see website: www.iwt.be Payroll costs (human resources and real salary costs) Other costs Direct costs Indirect costs Subcontractors Technicalities TGO-programme Subsidy Total project subsidy between 1.000.000 EUR and 3.500.000 EUR. Subsidy percentage differs per Module. Technicalities TGO-programme Subsidy Module 1 Research and Development Research: 50% Development: 25% Adaptive clinical trials: 37,5% Phase I/II clinical trials: 25% Phase III / Registration: 0% Module 2 Strategic Basic Research Research organisations: 100% Clinical centres: 100% Module 3 Applied Research Research organisations: 100% Clinical centres: 100% Technicalities TGO-programme Evaluation procedure 28 Technicalities TGO-programme Prior to submission 1. Information meeting Based on abstract (max. 2 pages) + specific questions Topics to be discussed: Fit of project proposal Programme related issues (budget, eligibility partners, etc.) Interested? Contact IWT: tgo@iwt.be Technicalities TGO-programme Prior to submission 2. Pre-registration meeting Deadline: November 26th, 2012 Based on preliminary project proposal Topics to be discussed: Consortium composition Project structure Valorisation Added value Budget Etc. Interested? Contact IWT: tgo@iwt.be Technicalities TGO-programme Prior to submission 2. Pre-registration meeting IMPORTANT: First time right! No instruction meeting! Project proposals cannot be changed once they are submitted. Technicalities TGO-programme Submission Deadline: December 17th, 2012 12:00 (Noon) Technicalities TGO-programme Submission Electronic submission (E-mail tgo@iwt.be (max 10 MB) or CD-rom) Submission according to the template on the website Technicalities TGO-programme Eligibility Formal eligibility criteria (See TGO-manual for complete list) On time? According to template? Consortium composition Etc. Decision: January 8th, 2013 Technicalities TGO-programme Evaluation IWT consults at least 4 international experts per project proposal Two general evaluation dimensions: Quality Social and economic valorisation Module specific criteria Technicalities TGO-programme Evaluation Quality Project focuses on the development of more effective and affordable drugs Contribution to the current state of the art Relevance of the scientific approach Risks and feasibility of the scientific approach Quality project plan Project management and track record Competence and infrastructure Technicalities TGO-programme Evaluation Social and economic valorisation Valorisation potential and feasibility valorisation goals Relevance project for valorisation goals Social impact of project results Economic impact of project results Competence and track record Broad utilisation Added value compared to existing IWT programs Technicalities TGO-programme Evaluation Module specific criteria Quality Social and economic valorisation Technicalities TGO-programme Evaluation Decision: Meeting Board of Directors April 2013. Technicalities TGO-programme Tips and tricks Carefully read the documents on the website and contact IWT in case of questions (tgo@iwt.be) Before you start writing your full proposal, send an abstract of the proposal to tgo@iwt.be in order to get some feedback regarding the fit of your project in the program Ask for a pre-registration meeting Technicalities TGO-programme Tips and tricks Make sure your project has a clear focus Make sure the project modules are integrated Make sure the scientific goals are in line with the valorisation goals Go for an innovative approach (risk and added value state of the art) Etc. Technicalities TGO-programme Timing: Opening call June 2012 Submission deadline December 17th, 2012 12:00 (Noon) Eligibility January 8th, 2013 Funding decision April 18th, 2013 42 Technicalities TGO-programme More information: http://www.iwt.be/subsidies/tgo tgo@iwt.be IWT Team: Liesbeth Biesmans Mia Callens Hendrik De Bondt Patricia Menten Dirk Veelaert Katrien Swerts (Programme coordinator) Maarten Sileghem (Responsible director) 43 agentschap voor Innovatie door Wetenschap en Technologie Koning Albert II-laan 35, bus 16 B-1030 Brussel Tel.: +32 (0)2 432 42 00 Fax.: +32 (0)2 432 43 99 E-mail: info@iwt.be www.iwt.be