TheraRadar
Data updated: May 26, 2026

XYWAV (calcium oxybate)

Sleep Approved 2020-07-21

XYWAV is indicated for the treatment of Cataplexy; Excessive Daytime Sleepiness; Narcolepsy; Idiopathic Hypersomnia.

How XYWAV Works

XYWAV is a mixture of calcium, magnesium, potassium, and sodium oxybates (gamma-hydroxybutyrate). While the exact mechanism of action is unknown, gamma-hydroxybutyrate (GHB) is an endogenous metabolite of the neurotransmitter GABA. It is hypothesized that the therapeutic effects of XYWAV are mediated through GABA$_B$ actions during sleep at noradrenergic, dopaminergic, and thalamocortical neurons.

2
Indications
--
Phase 3 Trials
2
Priority Reviews
5
Years on Market

Details

Status
Prescription
First Approved
2020-07-21
Patent Cliff
2041
Revenue
$465M (Q4-2025)

Pro Metrics

Patent cliff and revenue data

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Routes
ORAL
Dosage Forms
SOLUTION

XYWAV Approval History

2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
14 FDA actions from 2020 to 2025 · 1 indication expansions
Jul 2025 SUPPL
Update · REMS
May 2025 SUPPL
Update · REMS
Nov 2024 SUPPL
Update · REMS

What XYWAV Treats

4 indications

XYWAV is approved for 4 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.

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

XYWAV Boxed Warning

CENTRAL NERVOUS SYSTEM DEPRESSION and ABUSE AND MISUSE. • Central Nervous System Depression XYWAV is a CNS depressant. Clinically significant respiratory depression and obtundation may occur in patients treated with XYWAV at recommended doses [see Warnings and Precautions ( 5.1 , 5.4 )]. Many patients who received XYWAV during clinical trials in narcolepsy and idiopathic hypersomnia were receiving central nervous system stimulants [see Clinical Studies ( 14.1 , 14.2 , 14.3 )]. • Abuse and Misuse...

XYWAV Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to XYWAV

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

LUMRYZ
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AVADEL CNS
Shared indications:
CataplexyExcessive Daytime SleepinessNarcolepsy
WAKIX
PITOLISANT HYDROCHLORIDE
3 shared
HARMONY
Shared indications:
Excessive Daytime SleepinessCataplexyNarcolepsy
XYREM
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3 shared
JAZZ PHARMS
Shared indications:
CataplexyExcessive Daytime SleepinessNarcolepsy
📋

Clinical Trial Registry

1 trials
Trial Sponsor ID Phase Status Title
NCT06421532 Clear-Brain P23.100 Ph 2 enrolling by invitation Stimulating Amyloid Clearance in Cerebral Amyloid Angiopathy
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Active Pipeline

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Key Completed Trials

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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.

XYWAV FDA Label Details

Indications & Usage

FDA Label (PDF)

XYWAV is indicated for the treatment of Cataplexy; Excessive Daytime Sleepiness; Narcolepsy; Idiopathic Hypersomnia.

⚠️ BOXED WARNING

WARNING: CENTRAL NERVOUS SYSTEM DEPRESSION and ABUSE AND MISUSE. • Central Nervous System Depression XYWAV is a CNS depressant. Clinically significant respiratory depression and obtundation may occur in patients treated with XYWAV at recommended doses [see Warnings and Precautions ( 5.1 , 5.4 )]. Ma...

View full patent landscape →
21 OB patents · 4 families · 144 international docs across 27 countries

XYWAV Patents & Exclusivity

Latest Patent: Feb 2041
Exclusivity: Aug 2028

Patents (22 active)

US12138233 Expires Feb 22, 2041
US12582622 Expires Feb 22, 2041
US11426373 Expires Sep 19, 2037
US11253494*PED Expires Sep 15, 2033
US9050302*PED Expires Sep 15, 2033
US10213400*PED Expires Sep 15, 2033
US9486426*PED Expires Sep 15, 2033
US8772306*PED Expires Sep 15, 2033
US10864181*PED Expires Sep 15, 2033
US8772306 Expires Mar 15, 2033
US11986446 Expires Mar 15, 2033
US9050302 Expires Mar 15, 2033
US10213400 Expires Mar 15, 2033
US9486426 Expires Mar 15, 2033
US10864181 Expires Mar 15, 2033
US11253494 Expires Mar 15, 2033
US10675258 Expires Jan 11, 2033
US9132107 Expires Jan 11, 2033
US8901173 Expires Jan 11, 2033
US10195168 Expires Jan 11, 2033
US8591922 Expires Jan 11, 2033
US11554102 Expires Jan 11, 2033

Exclusivity

ODE-361 Until Jul 2027
ODE-369 Until Aug 2028
PED Until Jan 2028
Source: FDA Orange Book

Pro Intelligence Preview

Deep insights for XYWAV

Revenue Insights

  • Q4-2025: $465M
  • Historical trend analysis

Patent Timeline

  • Cliff: 2041
  • 25 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 20 similar drugs
  • Same target/indication analysis
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Data Sources

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