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Preclinical Trials:  A Nuanced Approach to Get Into the Clinic Faster A Q&A with Dr. Mike McGarry, who describes a nuanced preclinical process that can help a Chief Medical Officer get into the clinic faster. This approach hinges on a strategic, well-defined rodent model, quality data, and ongoing integration between the preclinical, regulatory and clinical teams.
Welcome ,[object Object],[object Object]
Preclinical Trials:  A Nuanced Approach to Get Into the Clinic Faster ,[object Object],[object Object]
About Dr. Mike McGarry, VP of Preclinical Studies ,[object Object],[object Object]
Mike, when a sponsor initiates a new preclinical study, what are the most important factors for a Chief Medical Officer to understand/ evaluate during this step in the drug development process? ,[object Object],[object Object],[object Object]
How rigorous is the regulatory assessment at the preclinical stage? ,[object Object],[object Object]
How common is it for a company to hit a regulatory wall at this stage? ,[object Object],[object Object]
How can a CMO work with the preclinical team to gain a better understanding of these complexities?  ,[object Object],[object Object]
So the sooner you bridge any gaps between preclinical and clinical, the better? ,[object Object],[object Object]
It sounds as if preclinical and clinical teams often operate independently in their own silos.  True? ,[object Object]
Can you discuss the typical preclinical process and the questions a CMO should be asking during this phase? ,[object Object],[object Object],[object Object]
Can you discuss the typical preclinical process and the questions a CMO should be asking during this phase? [continued]  ,[object Object],[object Object],[object Object]
Are there any additional requirements unique to oncology preclinical trials? ,[object Object]
What’s the typical time frame for a preclinical study? ,[object Object],[object Object]
You have over three decades’ experience conducting animal studies. How important is depth of experience on the part of the preclinical investigator? ,[object Object],[object Object],[object Object]
What would you look for in an outside preclinical team?  ,[object Object]
Can you discuss GLPs for preclinical work - are they always required? ,[object Object],[object Object]
Many groups have pushed for the elimination of animal-based studies. Is that a likely scenario down the road?  ,[object Object],[object Object]
Can computational toxicology diminish the reliance on animal models in the future? ,[object Object]
How might personalized medicine affect preclinical work? ,[object Object]
So the animal model is here to stay? ,[object Object]
About “Peer Perspectives in Oncology” ,[object Object],[object Object]
About Medelis ,[object Object],[object Object]

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Preclinical Trials: A Nuanced Study Process to Get Into the Clinic Faster

  • 1. Preclinical Trials: A Nuanced Approach to Get Into the Clinic Faster A Q&A with Dr. Mike McGarry, who describes a nuanced preclinical process that can help a Chief Medical Officer get into the clinic faster. This approach hinges on a strategic, well-defined rodent model, quality data, and ongoing integration between the preclinical, regulatory and clinical teams.
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