TheraRadar

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Data updated: Mar 10, 2026

DOPTELET

AVATROMBOPAG MALEATE
Immunology Approved 2018-05-21
3
Indications
--
Phase 3 Trials
1
Priority Reviews
7
Years on Market

Details

Status
Prescription
First Approved
2018-05-21
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: AVATROMBOPAG MALEATE

DOPTELET Approval History

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What DOPTELET Treats

3 indications

DOPTELET is approved for 3 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Thrombocytopenia
  • Chronic Liver Disease
  • Immune Thrombocytopenia
Source: FDA Label
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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

DOPTELET FDA Label Details

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Indications & Usage

FDA Label (PDF)

DOPTELET is a thrombopoietin receptor agonist indicated for the treatment of: Thrombocytopenia in adult patients with chronic liver disease who are scheduled to undergo a procedure. Thrombocytopenia in adult patients with chronic immune thrombocytopenia who have had an insufficient response to a previous treatment. Thrombocytopenia in pediatric patients 1 year and older with persistent or chronic immune thrombocytopenia who have had an insufficient response to a previous treatment 1.1 Treatment of Thrombocytopenia in Patients with Chronic Liver Disease (CLD) DOPTELET is indicated for the treat...

DOPTELET Patents & Exclusivity

Latest Patent: Jul 2027
Exclusivity: Jul 2028

Patents (1 active)

US7638536 Expires Jul 28, 2027

Exclusivity

I-974 Until Jul 2028
ODE-246 Until Jun 2026
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.