Five Scientific Posters Supporting the Efficacy and Tolerability of Once-Daily
Lurasidone - A New Atypical Antipsychotic Treatment for Adults with
BARCELONA, Spain, October 14, 2013
BARCELONA, Spain, October 14, 2013 /PRNewswire/ --
On the occasion of the26 ^th European College of Neuropsychopharmacology
Congress (ECNP), with educational financial support provided by Takeda and
Sunovion Pharmaceuticals Europe, new data was presented showing both short and
long-term efficacy for lurasidone, an atypical antipsychotic treatment for
schizophrenia. These data also showed lurasidone to have early separation from
placebo, a rapid onset of action ^ , a favourable side effect profile ^[
^1] ^, ^ ^, ^ ^, ^[ ^4] and to be a well-tolerated, efficacious option
for patients with schizophrenia switching medication. ^ Lurasidone has been
approved in US, Canada and Switzerland and is currently under regulatory
review in Europe.
The data included a post-hoc analysis of double-blind controlled studies
showing how insight (awareness of illness), when measured by PANSS score, was
significantly improved for clinically unstable patients given once-daily
lurasidone 80 mg, lurasidone 160 mg and active control quetiapine XR 600 mg,
compared to placebo, after 6 weeks ^ . At week 32, insight was
significantly greater for those treated with lurasidone compared with
quetiapine XR. Increased insight was shown to predict improvements in specific
Two post-hoc pooled analyses of a number of short-term trials demonstrated
that lurasidone is an efficacious treatment with a favourable safety profile.
One analysis demonstrated that lurasidone has early separation from placebo by
Week 1 and that the 160 mg dosage may provide significant additional efficacy
benefit. ^[ ^1] Side-effects were minimal regarding weight-gain, metabolic
parameters and prolactin. The second analysis looked at patients with
early-stage schizophrenia, as evidence suggests that they may be particularly
sensitive to antipsychotics in general. ^[ ^2] In both analyses, those treated
with lurasidone experienced significantly greater improvement at Week 6
compared with placebo on PANSS total and subscale scores (positive and
negative) and CGI-Severity score.
"As a dedicated psychiatrist, I am interested in new, effective agents for the
treatment of severely ill patients with mental disorders. This is particularly
true for patients who are not suitable for or who have not responded to
currently approved therapeutics. We need effective, well-tolerated and
metabolically neutral alternatives, which can also be used in young patients.
Lurasidone has an interesting profile of action." says Dr Philipp Eich, Stv
Chefarzt, Kantonale Psychiatrische Klinik Liestal, Switzerland.
A further presentation of the results of two randomized controlled long-term
(12-month) trials provided a head-to-head comparison of the safety and
effectiveness of lurasidone and quetiapine XR (D1050234), and lurasidone and
risperidone (D1050237). ^[ ^3] Lurasidone's side-effect profile was favourable
compared to quetiapine XR. The safety profile showed, in part, clinically
significant weight gain (defined as ≥7% weight gain from baseline) in 7.0% and
14.0% of patients treated with lurasidone vs risperidone, and in 11.5% and
15.2% of patients treated with lurasidone vs quetiapine, respectively.
Median changes in prolactin from baseline at month 12 were 0.0/+0.95 ng/ml
(for lurasidone, male/female) and +7.5/+24.6 ng/ml (for risperidone,
male/female). Overall, results of these two double-blind 12 month trials
suggest that lurasidone was effective and well-tolerated over 12 months of
Minimal changes in weight and lipid parameters were also shown after 6 months
in data evaluating the safety, tolerability and effectiveness of switching
other antipsychotic medication to lurasidone. ^[ ^4] Switching antipsychotic
medication is common in schizophrenia treatment either due to residual or
emergent symptoms, adverse events or tolerability issues. Data from a
randomized open-label switch extension study showed that lurasidone was
well-tolerated and that switched patients generally maintained or improved
their control of symptoms. ^[ ^4]
"Schizophrenia can have a devastating effect on people's lives, and they, and
the healthcare professionals who treat them, need a broader range of effective
treatment choices. Takeda is committed to bringing innovative medicines to
areas of unmet clinical need, offering benefits to the widest range of
patients possible." said Rene Gilvert, Vice President Global Marketing and
Therapeutic Area Lead CNS, Takeda Pharmaceuticals International.
"The data show lurasidone provides efficacy in multiple aspects of the complex
illness of schizophrenia. Lurasidone has a low incidence of side effects
observed, whilst providing needed efficacy for patients with schizophrenia."
said Tony Hale, Medical Director, Sunovion Pharmaceuticals Europe.
Takeda has submitted a marketing authorization application (MAA) for
lurasidone in October 2012 to the European Medicines Agency (EMA). Takeda will
communicate the outcome of this application in the coming months.
Lurasidone is an atypical antipsychotic, developed originally by Dainippon
Sumitomo Pharma Co., Ltd. (DSP) with an affinity for dopamine D2, serotonin
5-HT2A and serotonin 5-HT7 receptors where it has antagonist effects. In
addition, lurasidone is a partial agonist at the serotonin 5-HT1A receptor and
has no appreciable affinity for histamine or muscarinic receptors. Lurasidone
(brand name LATUDA ^® in Switzerland, Canada and the United States) was
approved for the treatment of schizophrenia by the United States Food and Drug
Administration in October 2010 and by Health Canada in June 2012. Lurasidone
was launched in the United States for the treatment of schizophrenia in adults
in February, 2011 and in Canada in September, 2012 through DSP's subsidiary
Sunovion Pharmaceuticals Inc. An application has been filed with the
Australian Therapeutic Goods Administration for the treatment of patients with
schizophrenia, and development in the Chinese and Southeast Asian markets is
planned. Additionally, Lurasidone received FDA approval for the treatment of
patients with major depressive episodes associated with bipolar I disorder
(bipolar depression) in June 2013.
The data presented include posters that were jointly developed by Sunovion
Pharmaceuticals Inc., the U.S. subsidiary of Dainippon Sumitomo Pharma Co.
Ltd. (DSP) and Takeda.
Schizophrenia is a severe chronic mental condition which can affect both men
and women. Patients with schizophrenia have a life span that is decreased by
approximately 10-22.5 years compared with the general population. ^ , ^
, ^ , ^
Antipsychotic pharmacotherapy is the cornerstone of treatment for patients
with schizophrenia, with agents generally classed as typical or atypical.
Atypical agents are broadly considered to have tolerability benefits over
typical agents. ^ Switching antipsychotic medication is common in the
treatment of patients with schizophrenia either due to residual or emergent
symptoms, adverse events or tolerability issues. ^ ^, ^
Direct and indirect costs associated with caring for patients with
schizophrenia are considerable and can include utilization of other health
services, pharmacotherapy, community care, supportive therapy, informal care
and private expenditures, and patient and caregiver lost productivity. ^
^, ^ Hospitalization associated with patient relapse can significantly
increase costs associated with disease management in schizophrenia. ^
About Takeda Pharmaceuticals International GmbH
Takeda Pharmaceuticals International GmbH, headquartered in Zurich, is a
wholly owned subsidiary of Takeda Pharmaceutical Company Limited. As the
largest pharmaceutical company in Japan and a leader in the global industry,
Takeda's mission is to strive toward better health for patients worldwide
through leading innovation in medicine. It has a commercial presence covering
more than 70 countries, with particular strength in Asia, North America,
Europe and fast-growing emerging markets including Latin America, Russia-CIS
and China. Takeda is ranked 12th by global Rx sales, 14th in the BRIC
countries and 18th in Europe. Takeda's commercial presence mainly covers the
therapeutic areas of metabolic diseases, gastroenterology, oncology,
cardiovascular health, CNS diseases, inflammatory and immune disorders,
respiratory diseases and pain management. Additional information about Takeda
is available through its corporate website, http://www.takeda.com .
About Sunovion Pharmaceuticals Europe Ltd.
Sunovion Pharmaceuticals Europe headquartered in London, a wholly owned
subsidiary of Dainippon Sumitomo Pharma Co., Ltd., defines its corporate
mission as "to broadly contribute to society through value creation based on
innovative research and development activities for the betterment of
healthcare and fuller lives for people worldwide". Sunovion Europe is focused
on the development and introduction of innovative medicines that improve
people's health and wellbeing. The Company's focus is in Psychiatry and
Neurology, including mental illness, and other disease areas of significant
unmet need which require highly specialised drug development. Additional
information about Sunovion Europe is available through its corporate website
This press release does not necessarily reflect the opinions of ECNP.
1.Murthy et al. Lurasidone for the treatment of schizophrenia: pooled
analysis of short-term, placebo-controlled trials (Abstract presented at ECNP,
8 October 2013)
2. Lieberman J.A. et al. Lurasidone in the treatment of early-stage
schizophrenia: a post-hoc analysis of three pooled acute treatment studies
(Abstract presented at ECNP, 8 October 2013)
3.Pikalov A.et al. Comparative effectiveness of long-term treatment with
atypical antipsychotics in patients with schizophrenia (Abstract presented at
ECNP, 8 October 2013)
4.McEvoy J.P.et al. Switching to lurasidone in patients with schizophrenia:
tolerability and effectiveness at 6 weeks and 6 months (Abstract presented at
ECNP, 8 October 2013)
5.Harvey P. et al. Impact of improved insight in schizophrenia: a
double-blind lurasidone and quetiapine XR study (Abstract presented at ECNP, 8
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Date of preparation: October 2013 Job number: EUCAN/LUR/2013-10016g
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