TheraRadar
Data updated: Mar 29, 2026

DOJOLVI

TRIHEPTANOIN
Approved 2020-06-30

Dojolvi (triheptanoin) is a medium-chain triglyceride indicated for the treatment of adult and pediatric patients with molecularly confirmed long-chain fatty acid oxidation disorders (LC-FAOD). The drug serves as a specialized source of calories and fatty acids for individuals managing these metabolic conditions. It provides a therapeutic nutritional intervention to support energy requirements in patients who cannot properly process long-chain fats.

Source: FDA Label • ULTRAGENYX PHARM INC • Medium-chain Triglyceride

How DOJOLVI Works

Triheptanoin is a medium-chain triglyceride consisting of three odd-chain, 7-carbon length fatty acids known as heptanoate. These fatty acids provide a source of calories and lipids that bypass the specific enzyme deficiencies associated with long-chain fatty acid oxidation disorders. By circumventing these metabolic blocks, the drug enables the body to produce energy and replace necessary fatty acids.

1
Indication
--
Phase 3 Trials
5
Years on Market

Details

Status
Prescription
First Approved
2020-06-30
Routes
ORAL
Dosage Forms
LIQUID

Companies

Active Ingredient: TRIHEPTANOIN

DOJOLVI Approval History

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What DOJOLVI Treats

1 indications

DOJOLVI is approved for 1 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Long-Chain Fatty Acid Oxidation Disorders
Source: FDA Label
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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.

DOJOLVI FDA Label Details

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Indications & Usage

FDA Label (PDF)

DOJOLVI is indicated as a source of calories and fatty acids for the treatment of adult and pediatric patients with molecularly confirmed long-chain fatty acid oxidation disorders (LC-FAOD). DOJOLVI is a medium-chain triglyceride indicated as a source of calories and fatty acids for the treatment of adult and pediatric patients with molecularly confirmed long-chain fatty acid oxidation disorders (LC-FAOD).

DOJOLVI Patents & Exclusivity

Latest Patent: Apr 2029
Exclusivity: Jun 2027

Patents (1 active)

US8697748 Expires Apr 28, 2029

Exclusivity

ODE-311 Until Jun 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.