TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

XYREM

SODIUM OXYBATE
Approved 2002-07-17
5
Indications
--
Phase 3 Trials
2
Priority Reviews
23
Years on Market

Details

Status
Prescription
First Approved
2002-07-17
Routes
ORAL
Dosage Forms
SOLUTION

Companies

Active Ingredient: SODIUM OXYBATE

XYREM Approval History

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What XYREM Treats

3 indications

XYREM is approved for 3 conditions since its original approval in 2002. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Cataplexy
  • Excessive Daytime Sleepiness
  • Narcolepsy
Source: FDA Label

XYREM Boxed Warning

CENTRAL NERVOUS SYSTEM DEPRESSION and ABUSE AND MISUSE. • Central Nervous System Depression Xyrem (sodium oxybate) is a CNS depressant. In clinical trials at recommended doses, obtundation and clinically significant respiratory depression occurred in adult patients treated with Xyrem [see Warnings and Precautions ( 5.1 )]. Many patients who received Xyrem during clinical trials in narcolepsy were receiving central nervous system stimulants [see Clinical Trials ( 14 )]. • Abuse and Misuse Xyrem ®...

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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.

XYREM FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

Xyrem is indicated for the treatment of cataplexy or excessive daytime sleepiness (EDS) in patients 7 years of age and older with narcolepsy. Xyrem is a central nervous system depressant indicated for the treatment of cataplexy or excessive daytime sleepiness (EDS) in patients 7 years of age and older with narcolepsy .

⚠️ BOXED WARNING

WARNING: CENTRAL NERVOUS SYSTEM DEPRESSION and ABUSE AND MISUSE. • Central Nervous System Depression Xyrem (sodium oxybate) is a CNS depressant. In clinical trials at recommended doses, obtundation and clinically significant respiratory depression occurred in adult patients treated with Xyrem [see W...

XYREM Patents & Exclusivity

Latest Patent: Sep 2033
Exclusivity: Apr 2026

Patents (14 active)

US8772306*PED Expires Sep 15, 2033
US9486426*PED Expires Sep 15, 2033
US9050302*PED Expires Sep 15, 2033
US11253494*PED Expires Sep 15, 2033
US10213400*PED Expires Sep 15, 2033
US10864181*PED Expires Sep 15, 2033
US10213400 Expires Mar 15, 2033
US9486426 Expires Mar 15, 2033
US9050302 Expires Mar 15, 2033
US8772306 Expires Mar 15, 2033
+ 4 more patents

Exclusivity

ODE-231 Until Oct 2025
PED Until Apr 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.