2008
DOI: 10.1038/nm0308-226b
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Despite potential side effects, two drugs make a comeback

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Cited by 4 publications
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“…To explain this logic, we breakdown the trials process. Phase‐0 (not a mandatory step, but becoming increasingly common in cancer research) is designed to validate that the intended target can be hit or that a drug can enter the blood stream in humans at low dose [314] . Phase‐I usually focuses on gross tolerance/side effects and pharmacokinetics/pharmacodynamics.…”
Section: Choice Of Compounds To Be Evaluated In Rapid Screening Clinical Trialsmentioning
confidence: 99%
“…To explain this logic, we breakdown the trials process. Phase‐0 (not a mandatory step, but becoming increasingly common in cancer research) is designed to validate that the intended target can be hit or that a drug can enter the blood stream in humans at low dose [314] . Phase‐I usually focuses on gross tolerance/side effects and pharmacokinetics/pharmacodynamics.…”
Section: Choice Of Compounds To Be Evaluated In Rapid Screening Clinical Trialsmentioning
confidence: 99%
“…Failure beyond this point indicates, in many instances, more about the application of the drug in a specific context, or contexts. In this way, looking at candidates that have entered Phase-II trials (incidentally, where the majority of drugs fail) and above (and even those withdrawn if not due to adverse side effects, or with manageable contraindications) 314 can help to broaden the scope of screening programs. Such experiments can be performed with knowledge of toxicity and having ideas about, e.g., tolerated doses, pharmacokinetics, in humans.…”
Section: Targeting Infection and Harnessing Fortuitous Antiviral Effementioning
confidence: 99%