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Research Protocols & Dosing Insights Dosing parameters reported in the preclinical literature vary by species, injury model, administration route, and research objective

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[Our] basic thinking on AOD9604 is that the drug failed because it was made orally available, which likely reduced bioavailability and also potentially resulted in protein denaturisation in the gastrointestinal tract, which would have reduced the drugs activity

A: This product is formulated for intravenous (IV), intramuscular (IM), subcutaneous (SC), and intradermal (ID) administration routes