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Pharmacokinetic studies revealed [6] : Orally administered AOD9604 was well absorbed in pigs with rapid degradation kinetics Primary degradation products were peptide fragments missing 2-3 amino acids from termini Both degradation products retained some reduced anti-lipogenic activity Rat whole-body radiography showed similar organ distribution patterns following both intravenous and oral administration This distribution pattern supports systemic absorption via the oral route in laboratory models

reconstituted solutions should not be frozen unless explicitly stated in the SmPC

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