TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

LYTGOBI

FUTIBATINIB
Approved 2022-09-30
1
Indication
--
Phase 3 Trials
1
Priority Reviews
3
Years on Market

Details

Status
Prescription
First Approved
2022-09-30
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: FUTIBATINIB

LYTGOBI Approval History

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What LYTGOBI Treats

1 FDA approvals

Originally approved for its first indication in 2022 .

  • Other (1)
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Active Pipeline

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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.

LYTGOBI FDA Label Details

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LYTGOBI Patents & Exclusivity

Latest Patent: Nov 2039
Exclusivity: Sep 2029

Patents (12 active)

US11833151 Expires Nov 5, 2039
US10434103 Expires Mar 31, 2036
US9108973 Expires Feb 13, 2033
+ 2 more patents

Exclusivity

NCE Until Sep 2027
ODE-410 Until Sep 2029
NCE Until Sep 2027
ODE* Until Sep 2029
NCE Until Sep 2027
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.