Update 'Hypotheses: Trial Duration/dyanimcs'
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following line of questioning Abrantes-Metz, Adams, & Metz
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questions revolve around the durations of trials.
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# specific questions
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## Does successful completion/other dynamics depend on the market for which the drug is being tested?
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So, for example are trials more likely to terminate if there are a lot of other drugs on that market? Are trials more likely to last longer if it is a generic or other second to market?
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Those types of questions can be answered by my dataset. Basically, do dynamics shift based on market saturation? How does that change across phases?
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## quantile duration
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- Do trials whose trial duration was in a higher quantile remain within higher quantile for later trials? i.e. are durations stable?
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- Is there a policy which shuffles durations?
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- using quantile methods might allow one to create estimates including trials that are not complete.
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following line of questioning Abrantes-Metz, Adams, & Metz
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questions revolve around the durations of trials.
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# specific questions
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## quantile duration
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- Do trials whose trial duration was in a higher quantile remain within higher quantile for later trials? i.e. are durations stable?
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- Is there a policy which shuffles durations?
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- using quantile methods might allow one to create estimates including trials that are not complete.
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