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Data updated: Mar 10, 2026

TURALIO

PEXIDARTINIB HYDROCHLORIDE
Oncology Approved 2019-08-02
3
Indications
--
Phase 3 Trials
1
Priority Reviews
6
Years on Market

Details

Status
Prescription
First Approved
2019-08-02
Routes
ORAL
Dosage Forms
CAPSULE

Companies

Active Ingredient: PEXIDARTINIB HYDROCHLORIDE

TURALIO Approval History

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What TURALIO Treats

1 indications

TURALIO is approved for 1 conditions since its original approval in 2019. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Tenosynovial Giant Cell Tumor
Source: FDA Label

TURALIO Boxed Warning

HEPATOTOXICITY TURALIO can cause serious and potentially fatal liver injury, including vanishing bile duct syndrome [see Warnings and Precautions (5.1) ] . Monitor liver tests prior to initiation of TURALIO and at specified intervals during treatment. Withhold and dose reduce or permanently discontinue TURALIO based on severity of hepatotoxicity. Monitoring and prompt cessation of TURALIO may not eliminate the risk of serious and potentially fatal liver injury [see Dosage and Administration (2.2...

TURALIO Competitors

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10 other drugs also target KIT. Compare mechanisms, indications, and trial activity.

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Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications → Date = Patent/exclusivity expiry

Competitors share the same molecular target (KIT). Earlier expiry dates signal biosimilar/generic opportunities.

Drugs Similar to TURALIO

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

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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.

TURALIO FDA Label Details

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Indications & Usage

FDA Label (PDF)

TURALIO is indicated for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT) associated with severe morbidity or functional limitations and not amenable to improvement with surgery. TURALIO is a kinase inhibitor indicated for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT) associated with severe morbidity or functional limitations and not amenable to improvement with surgery.

⚠️ BOXED WARNING

WARNING: HEPATOTOXICITY TURALIO can cause serious and potentially fatal liver injury, including vanishing bile duct syndrome [see Warnings and Precautions (5.1) ] . Monitor liver tests prior to initiation of TURALIO and at specified intervals during treatment. Withhold and dose reduce or permanently...

TURALIO Patents & Exclusivity

Latest Patent: Jul 2038
Exclusivity: Aug 2026

Patents (48 active)

US10961240 Expires Jul 24, 2038
US10941142 Expires Jul 24, 2038
US10435404 Expires Jul 24, 2038
US10189833 Expires May 5, 2036
US10730876 Expires May 5, 2036
US9802932 Expires May 5, 2036
US9358235 Expires Jun 8, 2033
US7893075 Expires May 4, 2033
US8461169 Expires Apr 19, 2028
US8404700 Expires Nov 21, 2027
+ 38 more patents

Exclusivity

ODE-250 Until Aug 2026
ODE* Until Aug 2026
ODE-250 Until Aug 2026
ODE* Until Aug 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.