Bioprojet: European Marketing Authorisation for OZAWADEtm

EXCESSIVE DAYTIME SLEEPINESS IN OBSTRUCTIVE SLEEP APNOEA SYNDROME (OSAD)

EUROPEAN MARKETING AUTHORISATION FOR OZAWADEtm

PARIS, Sept. 3, 2021 /PRNewswire/ -- The European Medicines Agency has issued a marketing authorisation for OZAWADEtm (pitolisant), indicated in the treatment of excessive daytime sleepiness (EDS) associated with obstructive sleep apnoea in adults.

OZAWADEtm is indicated to improve wakefulness and reduce EDS in adult patients suffering from obstructive sleep apnoea (OSA) whose EDS has not been treated satisfactorily by a primary treatment for OSA, such as continuous positive pressure (CPP); it is also indicated for those who do not tolerate CPP.

Pitolisant is a histamine H3 receptor antagonist/inverse agonist discovered by Jean-Charles Schwartz, his collaborators at Inserm and Société Bioprojet de Paris, with the assistance of two European chemists (Walter Schunack at Berlin University and Robin Ganellin at University College London). By blocking histamine autoreceptors, it increases the activity of cerebral histamine neurons, a major wakefulness system with projections extending to the entire brain. Pitolisant also increases the release of acetylcholine, noradrenaline and dopamine in the brain. Pitolisant was already indicated in Europe and the United States for the treatment of EDS and cataplexy in narcolepsy patients.

The efficacy and safety of pitolisant in the treatment of EDS in patients suffering from OSA has been investigated in two phase III multicentre, randomised, double-blind, placebo-controlled clinical studies: HAROSA I and HAROSA II. In the first, patients were treated with CPP but still complained of EDS. In the second, patients did not tolerate the CPP treatment and suffered from EDS.

The two studies showed a significant improvement in the Epworth Sleepiness Scale score (ESS) in patients treated with pitolisant. No notable cardiovascular incidents or significant change in blood pressure and heart rate were observed[1].

"With fatigue, excessive daytime sleepiness is the symptom most frequently reported by patients, with a considerable impact on quality of life and on daily safety," emphasises Jean-Charles Schwartz, scientific director and co-founder of Bioprojet. "OZAWADE provides an effective solution to all patients, whether they are treated by PPC or intolerant of this treatment.. The HAROSA I and II studies in particular demonstrated that taking pitolisant had no impact on systolic or diastolic blood pressure and did not increase the risk of hypertension^1,2. In fact, the mode of action for OZAWADE is distinct from that of psychostimulants which gives it a favourable safety profile, which is essential for a population which often has metabolic and cardiovascular co-morbidities³".

According to various epidemiology studies, 1 billion people globally have OSA with significant consequences on global health and the functioning of various organs⁴.  It is frequently associated with fatigue, awareness and concentration problems, irritability and symptoms of depression. The difficulties experienced by patients to cope with all the tasks of daily life have an impact on their quality of life and that of their family and friends, but also on the community (cost in terms of health, reduced productivity, increased risk of accidents)⁵.

About Bioprojet

Bioprojet laboratory was formed in 1982 under the initiative of two researchers, Jeanne-Marie Lecomte and Jean-Charles Schwartz, in order to bring together academic research and commercial pharmaceutical development, a not very widespread practice at the time.

Bioprojet's objective: lean on original fundamental research to design and develop medicines which, like pitolisant, would be the first of new therapeutic classes. 

Bioprojet is based in seven European countries and its research centre designs and investigates a thousand new molecules every year.

www.bioprojet.com   

Contact:

FINN Partners [email protected]

¹ Pépin et al. Pitolisant for Residual Excessive Daytime Sleepiness in OSA Patients Adhering to CPAP: A Randomized Trial, Chest Apr, 159(4): 1598-1609.

² Dauvilliers Y et al. Pitolisant for Daytime Sleepiness in Patients with Obstructive Sleep Apnea Who Refuse Continuous Positive Airway Pressure Treatment: A Randomized Trial. Am J Respir Crit Care Med. 2020 May. 1; 201(9): 1135?1145

³ McNicholas WT, Bassetti CL, Ferini- Strambi L, et al. Challenges in obstructive sleep apnoea. Lancet Respir Med. 2018;6(4):170-172.

⁴Bucks RS, Olaithe M, Rosenzweig I, Morrell MJ. Reviewing the relationship between OSA and cognition: where do we go from here? Respirology. 2017;22(7): 1253-1261.

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