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Doptelet (AVATROMBOPAG)

Akarx Inc · FDA-approved approved Small molecule Quality 65/100

Doptelet works by binding to the thrombopoietin receptor, stimulating platelet production in the bone marrow.

Doptelet (Avatrombopag) is a small molecule drug developed by Akarx Inc, targeting the thrombopoietin receptor. It was FDA-approved in 2018 for the treatment of thrombocytopenic disorders. Doptelet is a patented medication with no generic manufacturers available. Key safety considerations include its potential to cause bone marrow suppression and thrombocytosis. As a thrombopoietin receptor agonist, Doptelet works by stimulating platelet production in the bone marrow.

At a glance

Generic nameAVATROMBOPAG
SponsorAkarx Inc
TargetThrombopoietin receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval2018

Mechanism of action

Avatrombopag is an orally bioavailable, small molecule TPO receptor agonist that stimulates proliferation and differentiation of megakaryocytes from bone marrow progenitor cells, resulting in an increased production of platelets. Avatrombopag does not compete with TPO for binding to the TPO receptor and has an additive effect with TPO on platelet production.

Approved indications

Common side effects

Key clinical trials

Patents

PatentExpiryType

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

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