Table 1.
Hetrombopag | |||||
---|---|---|---|---|---|
Molecular structure | Peptide | Small molecule | Small molecule | Small molecule | Small molecule |
TPO receptor site of action | Extracellular domain | Transmembrane domain | Transmembrane domain | Transmembrane domain | Transmembrane domain |
Route of administration | Subcutaneous | Oral | Oral | Oral | Oral |
Dosing frequency a | Weekly | Daily | Daily or less frequently than daily | Daily | Daily |
Relevant food interactions | N/A | Yes | No | No | Yes |
Known hepatotoxicity | No | Yes | No | No | Yes |
Possible plasma, skin, and sclerae discoloration | No | Yes | No | No | No |
Iron chelator | No | Yes | No | No | Yes |
May require lower starting dose in persons of East Asian ethnicity | No | Yes | No | No | Yes |
Requires dose-reduction in hepatic dysfunction | No | Yes | No | No | Yes |
Demonstrated increased thrombosis risk in chronic liver disease | No | Yes | No | No | No |
Data exists for use in pregnancy b | Yes | Yes | No | No | No |
Safety data available for extended durationc use | Yes | Yes | No | No | No |
Current FDA-approved indications | Immune thrombocytopenia (adults and children) Acute radiation syndrome | Immune thrombocytopenia (adults and children) Hepatitis C-associated thrombocytopenia Severe aplastic anemia | Periprocedural thrombocytopenia in CLD patients Immune thrombocytopenia (adults) | Periprocedural thrombocytopenia in CLD patients | None (approved in China for management of immune thrombocytopenia and severe aplastic anemia) |
Per drug label. Like avatrombopag, eltrombopag can be dosed less frequently than once daily [73] though this is not in the drug label.
No TPO-RAs are approved for use in pregnancy for any indication. Available data in pregnancy is in patients with ITP.
Defined here as 5 or more years of continuous use.
TPO, thrombopoietin. CLD, chronic liver disease. N/A, not applicable.