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Pitolisant

Generic Name
Pitolisant
Brand Names
Wakix, Ozawade
Drug Type
Small Molecule
Chemical Formula
C17H26ClNO
CAS Number
362665-56-3
Unique Ingredient Identifier
4BC83L4PIY

Overview

Pitolisant is a selective antagonist or inverse agonist of the histamine H3 receptor used to treat type 1 or 2 narcolepsy. Narcolepsy is a chronic neurological disorder that affects 1 in 2,000 individuals and is characterized by excessive daytime sleepiness, abnormal REM sleep manifestations, sleep paralysis and hypnagogic hallucinations. About 60-70% of patients with narcolepsy experience cataplexy, which is a sudden loss of muscle tone triggered by positive or negative emotions. Histaminergic neuron signalling in the brain plays a role in maintaining wakefulness; by blocking histamine autoreceptors, pitolisant enhances the activity of histaminergic neurons, as well as increasing the signalling of other neurotransmitters in the brain. In a European clinical trial of adult patients with narcolepsy, there was a reduction in the Epworth Sleepiness Scale (ESS) score from pitolisant therapy compared to placebo. The therapeutic effectiveness of pitolisant was comparable to that of modafinil. Pitolisant therapy was also effective in treating refractory sleepiness in adolescent patients with narcolepsy, where it decreased ESS score and increased the mean sleep onset latency. Adolescent patients with cataplexy also experienced a slight improvement in the frequency and severity of symptoms ; however, the safety of use in adolescent or paediatric patients have not been established with pitolisant. Commonly marketed under the trade name Wakix, oral pitolisant was approved by the EMA in 2016 for the treatment of narcolepsy with or without cataplexy. FDA approved the use of pitolisant in 2019 for excessive daytime sleepiness (EDS) associated with narcolepsy in adults.

Indication

Pitolisant is indicated for the treatment of narcolepsy with or without cataplexy and excessive daytime sleepiness in narcolepsy in adult patients.

Associated Conditions

  • Excessive Daytime Sleepiness
  • Narcolepsy With Cataplexy
  • Narcolepsy Without Cataplexy

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/04/16
Phase 3
Recruiting
2023/07/20
Phase 2
Not yet recruiting
2023/05/09
Not Applicable
Completed
2022/10/14
Phase 4
Recruiting
William Ondo, MD
2022/09/10
N/A
Recruiting
2022/07/14
Phase 3
Active, not recruiting
2022/02/03
Phase 3
Completed
Citrine Medicine Limited
2021/12/14
Phase 3
Completed
2021/05/14
Phase 2
Completed
2020/10/22
Phase 1
Terminated

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Harmony Biosciences, LLC
72028-178
ORAL
17.8 mg in 1 1
6/12/2025
Harmony Biosciences, LLC
72028-045
ORAL
4.45 mg in 1 1
6/12/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
9/1/2021
Authorised
3/31/2016

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
WAKIX
Endo Operations Ltd.
02516241
Tablet - Oral
5 MG
12/31/2021
WAKIX
Endo Operations Ltd.
02516268
Tablet - Oral
20 MG
12/31/2021

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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