Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Hetrombopag olamine is the orally active ethanolamine salt of hetrombopag, a small-molecule nonpeptide thrombopoietin receptor (TPO-R or CD110) agonist. It stimulates the transmembrane domain of the platelet TPO-R to promote proliferation and differentiation of megakaryocytic lineage cells and increase platelet production. This mechanism is used to treat thrombocytopenia in conditions such as immune thrombocytopenia (ITP) and severe aplastic anaemia (SAA), especially in patients who have not responded to or relapsed after first-line therapies like corticosteroids. "Standard therapy" typically refers to established treatments for ITP or SAA—most commonly corticosteroids for ITP—but may also include immunosuppressants or other supportive care depending on disease context[1][3][4][6]. The combination "hetrombopag olamine + standard therapy" thus refers to using hetrombopag alongside these established regimens.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on hetrombopag olamine + standard therapy.