Step 1
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Use available knowledge
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Bibliography
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(i) Pathophysiology, diagnosis, therapeutics, pharmacology |
(ii)Discursive and mathematical models for the disease |
(iii)Discursive and mathematical models for the drug effect(s) |
Individual epidemiological and RCT databases
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(i) Statistical approaches for analysis |
(ii) Identify prognostic biomarkers |
(iii) Identify N potential drugs (or therapeutic strategies) for evaluation in phase III RCTs |
(iv) Identify predictive biomarkers for these N drugs (e.g. interactions between patient characteristics and drug efficacy) |
(v) Validate drug-disease models |
Step 2
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Drug-disease modeling for the N treatments identified above
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Treatment 1: (Disease model + Drug effect model 1) |
Treatment i: (Disease model + Drug effect model i) |
Treatment N: (Disease model + Drug effect model N) |
Step 3
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Drug-disease modeling for the N treatments above in patients whose characteristics may interact with drug efficacy
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Treatment 1: (Disease model + Drug effect model 1) in patients whose specific characteristics interact with treatment effect 1 |
Treatment i: (Disease model + Drug effect model i) in patients whose specific characteristics interact with treatment effect i |
Treatment N: (Disease model + Drug effect model N) in patients whose specific characteristics interact with treatment effect N |
Step 4
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Experimental RCT design modeling (including orthogonal approaches) for N conditions above
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P experimental designs *N situations |
Step 5
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Simulate these N*P options
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Results ordered in terms of potential efficacy, adverse events, number of needed patients, cost (including trial duration) |
Step 6
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Identify the most relevant drugs to be evaluated in phase III RCTs and the RCT design to be used for each of them |
Multiple-criteria decision analysis approaches |