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**Avatrombopag + itraconazole** is a combination of the thrombopoietin receptor agonist avatrombopag and the antifungal agent itraconazole, primarily relevant in the context of drug-drug interaction studies. Avatrombopag acts as a small-molecule agonist of the thrombopoietin receptor (c-Mpl), stimulating proliferation and differentiation of megakaryocytes, thus increasing platelet production for the treatment of thrombocytopenia in chronic liver disease and chronic immune thrombocytopenia. Itraconazole is a strong cytochrome P450 3A (CYP3A) inhibitor used in antifungal therapy. Co-administration of these agents leads to a mild increase in avatrombopag exposure (AUC and Cmax) and a corresponding mild increase in its pharmacodynamic effects on platelet count, compared to monotherapy. This combination may require adjustment in avatrombopag dose or treatment duration due to pharmacokinetic modulation by itraconazole[1][2][3][4].
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