- Brexpiprazole's indication for the treatment of
schizophrenia in adults is extended to include adolescents aged 13
years and older1
- Approval follows a positive Committee for Medicinal Products
for Human Use (CHMP) opinion from the European Medicines Agency in
January 20252
- Treatment with brexpiprazole (2-4 mg/day) significantly
reduced the symptoms of schizophrenia as measured by PANSS total
score compared to placebo3
WINDSOR,
England and VALBY, Denmark, March 13,
2025 /PRNewswire/ -- Otsuka Pharmaceutical
Europe Ltd. (Otsuka) and H. Lundbeck A/S (Lundbeck) today announced
that the European Commission (EC) has approved
Rxulti® (brexpiprazole) for the treatment of
schizophrenia in adolescents aged 13 years and older.1
Brexpiprazole was previously approved in the European Union in
2018 for the treatment of schizophrenia in adults.4
The EC decision based its approval on a 6-week, randomised,
double-blind placebo-controlled and active-referenced trial of 316
adolescent patients, which evaluated the efficacy and safety
profile of the drug as primary and secondary outcomes,
respectively.3 Brexpiprazole (2-4mg/day) was associated
with greater reductions in symptom severity, as measured by the
Positive and Negative Syndrome Scale (PANSS) total score compared
with placebo in patients aged 13 years and older, and was generally
well tolerated with a safety profile consistent with that seen in
adult patients with schizophrenia.3
Andy Hodge, CEO at Otsuka
Pharmaceutical Europe, said: "The prognosis for adolescence-onset
schizophrenia is poor compared with adult-onset schizophrenia and
can be associated with more chronic and severe symptoms. We welcome
the EC decision to extend the indication for brexpiprazole to
include adolescents aged 13 years and older, providing young people
in Europe with another much-needed
treatment option."
Johan Luthman, EVP and Head of
Research & Development at Lundbeck, said: "Today marks a major
milestone for young patients, caregivers, and families navigating
the complexities of schizophrenia. This approval is testament to
our commitment and unwavering support to lessen the disease burden
for patients and caregivers in the EU, by providing a treatment
option with proven efficacy and tolerability."
About Rxulti® (brexpiprazole)
Brexpiprazole is an atypical oral antipsychotic that is taken
once a day.3 The pharmacology of brexpiprazole is
believed to be mediated by a modulatory activity at the serotonin
and dopamine systems that combines partial agonist activity at
serotonergic 5-HT1A and at dopaminergic D2 receptors with
antagonist activity at serotonergic 5-HT2A receptors, with similar
high affinities at all of these receptors. Brexpiprazole also shows
antagonist activity at noradrenergic α1B/2C receptors with affinity in the same
sub-nanomolar Ki range.4,5
Brexpiprazole was discovered by Otsuka and is being co-developed
and co-commercialised under a collaboration and license agreement
between Otsuka Pharmaceutical Europe Ltd. and H. Lundbeck A/S.
Brexpiprazole was previously approved in the European Union in
2018 for the treatment of adult patients with
schizophrenia.4
About schizophrenia
Schizophrenia is a chronic, disabling and progressive mental
illness, characterised by delusions, hallucinations, and disordered
cognition which may occur at varying intervals between periods of
relative symptomatic stability.5,7 Schizophrenia affects
approximately 24 million people, or 1 in 300 people (0.32%)
worldwide.8 Onset is most often during late adolescence
and the twenties, and onset tends to happen earlier among men than
women.8
Schizophrenia is frequently associated with significant distress
and impairment in personal, family, social, educational,
occupational, and other important areas of life.8 It is
one of the top 15 leading causes of disability
worldwide.9For adolescents with schizophrenia,
antipsychotics offer improvements in symptom control; however,
younger patients may be particularly vulnerable to side
effects.10,11,12
About Otsuka
Otsuka Pharmaceutical is a global healthcare company with the
corporate philosophy: "Otsuka-people creating new products for
better health worldwide."
Otsuka researches, develops, manufactures, and markets
innovative products, focusing on pharmaceutical products to meet
unmet medical needs and nutraceutical products for the maintenance
of everyday health. In pharmaceuticals, Otsuka is a leader in the
challenging area of mental health and also has research programmes
in several under-addressed diseases including tuberculosis, a
significant global public health issue.
Otsuka Europe employs around 500
people and focuses on psychiatric and neurologic disorders,
nephrology and immunology, haemato-oncology, and digital
therapeutics. Otsuka Pharmaceutical Europe Ltd. is a part of Otsuka
Pharmaceutical Company, Ltd., a subsidiary of Otsuka Holdings Co.,
Ltd. headquartered in Tokyo,
Japan.
The Otsuka group of companies employ approximately 35,340
people worldwide with consolidated sales of approximately € 14.1
billion and a spend of € 1.9 billion on research and development in
2024. For further information on Otsuka, please
visit www.otsuka-europe.com.
Otsuka contact for media
Alison Ross
Otsuka Pharmaceutical Europe Ltd.
ARoss@Otsuka-Europe.com
+44 776 833 7128
About H. Lundbeck A/S
Lundbeck is a biopharmaceutical company focusing exclusively on
brain health. With more than 70 years of experience in
neuroscience, we are committed to improving the lives of people
with neurological and psychiatric diseases.
Brain disorders affect a large part of the world's population,
and the effects are felt throughout society. With the rapidly
improving understanding of the biology of the brain, we hold
ourselves accountable for advancing brain health by curiously
exploring new opportunities for treatments.
As a focused innovator, we strive for our research and
development programs to tackle some of the most complex
neurological challenges. We develop transformative medicines
targeting people for whom there are few or no treatments available,
expanding into neuro-specialty and neuro-rare from our strong
legacy within psychiatry and neurology.
We are committed to fighting stigma and we act to improve health
equity. We strive to create long term value for our shareholders by
making a positive contribution to patients, their families and
society as a whole.
Lundbeck has approximately 5,500 employees in more than 50
countries and our products are available in more than 80
countries.
Lundbeck contacts
Investors:
Jens Høyer
Vice President, Head of Investor Relations,
JSHR@lundbeck.com
+45 30 83 45 01
Media:
Åsa Josefsson
Senior Director, Corporate Communication,
asjs@lundbeck.com
+45 30 83 42 50
References
- European Commission. Rxulti Product Information. Available at:
https://ec.europa.eu/health/documents/community-register/html/h1294.htm
Accessed: March 2025. Rxulti positive
CHMP opinion. Available at:
https://www.ema.europa.eu/en/medicines/human/variation/rxulti
Accessed: February 2025.
- Ward C, et al. Oral presentation at the 2024 Annual Congress of
the Schizophrenia International Research Society, Florence, Italy.
- Rxulti SmPC. Available from:
https://www.ema.europa.eu/en/documents/product-information/rxulti-epar-product-information_en.pdf
Accessed: February 2025.
- Maeda K, et al. J Pharmacol Exp Ther 2014; 350 (3):
589–604.
- Jain R, et al. J Clin Psychiatry 2024; 85 (4):
plunaro2417ah.
- Kahn RS, et al. Nat Rev Dis Primers 2015; 1
(15067).
- World Health Organisation. Factsheet, Schizophrenia. Available
from:
https://www.who.int/news-room/fact-sheets/detail/schizophrenia
Accessed: February 2025.
- Global Burden of Disease Study 2016. Lancet 2017; 390
(10100): 1211–1259.
- McClellan J & Stock S. J Am Acad Child Adolesc
Psychiatry 2013; 52 (9): 976–90.
- Olfson M, et al. Arch Gen Psychiatry 2012; 69 (12):
1247–56.
- Pagsberg AK, et al. J Am Acad Child Adolesc Psychiatry
2017; 56 (3): 191–202.
H. Lundbeck A/S
Ottiliavej 9, 2500 Valby, Denmark
+45 3630 1311
info@lundbeck.com
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Rxulti® approved in the
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