I agree that DJL is qualified from the medical/res
Post# of 157685

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I agree that DJL is qualified from the medical/research side, but is he assertive enough to push back, respectfully (starting with 700mg, for example instead of 350mg in trials.
If the FDA absolutely refuses then does he tell them that then we will not be doing the trial? You have very little leverage when dealing with a federal bureaucracy that holds sole dispositive power.
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There appears to be gobs of safety data to support, are there not)?
In widely disparate diseases the FDA will want to see the safety data by individual disease types. In cancer we have data from a small group of patients where the two trials were never finished and the study was an open-ended study. They may think that leronlimab is probably safe in cancer, but the first rule of bureaucracy is do things by the book to cover your ass.

