The evaluation of drug rechallenge: the casopitant Phase III program |
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Authors: | Hunt Christine M Papay Julie I Rich Donna S Abissi Christopher J Russo Mark W |
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Affiliation: | a GlaxoSmithKline, RTP, Durham, NC 27709, USA;b GlaxoSmithKline, Collegeville, PA 19426, USA |
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Abstract: | Drug rechallenge (or reinitiation), following an event of drug-induced liver injury, is associated with 13% mortality in prospective series. Rechallenge generally results in much more rapid injury than the initial liver event. The neurokinin-1 antagonist casopitant or its placebo was administered cyclically with ondansetron and dexamethasone in two randomized chemotherapy-induced nausea and vomiting clinical trials in nearly 3000 subjects. Grade 3 ALT elevations were observed in up to 2% of subjects receiving casopitant or placebo treatment. Similar rates of positive rechallenge were observed in the casopitant 8/29 (28%) and placebo groups 2/8 (25%), with no Grade 4 ALT elevations, hypersensitivity or liver-related serious adverse events. Publishing available rechallenge data (positive and negative) will advance our clinical understanding. Rechallenge should only be considered when the potential drug benefit exceeds the risk. |
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Keywords: | Rechallenge Drug-induced liver injury Hepatotoxicity Mitochondrial dysfunction Immunoallergic injury Liver injury Liver safety Clinical trial Casopitant |
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