04.04.2016 07:00:06
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DGAP-News: Newron Pharmaceuticals S.p.A.Az.
DGAP-News: Newron Pharmaceuticals S.p.A.: ZAMBON LAUNCHES XADAGO(R) (SAFINAMIDE) IN BELGIUM FOR PATIENTS WITH MID-TO LATE STAGE PARKINSON'S DISEASE
- Safinamide is a new chemical entity with a dopaminergic and non dopaminergic action, providing a balanced control of motor symptoms and motor complications
Milan, Italy - April 4, 2016 - Zambon S.p.A., an international pharmaceutical company strongly committed to the central nervous system (CNS) therapeutic area, and its partner Newron Pharmaceuticals S.p.A. ("Newron") (SIX: NWRN), a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central nervous system (CNS) and pain, today announced the launch of Xadago(R) (safinamide) in Belgium for the treatment of mid- to late stage Parkinson's disease (PD). Following the launch in Switzerland, Germany, Spain and Italy, Xadago(R) (safinamide) is now available in Belgium as add-on therapy to a stable dose of levodopa (L-dopa) alone or in combination with other PD therapies for mid-to late-stage fluctuating patients.
Safinamide is a new chemical entity with a dopaminergic and non-dopaminergic action, providing a balanced control of motor symptoms and motor complications.
Prof. Patrick Santens, from University Hospital Ghent commented: "Thanks to its unique dual dopaminergic and non-dopaminergic mode of action, including the modulation of altered glutamatergic neurotransmission, Xadago(R) (safinamide) has the potential to become a long awaited treatment alternative for our patients suffering from idiopathic Parkinson's disease with motor fluctuations".
Maurizio Castorina, CEO of Zambon SpA said: "We are glad to see health authorities across Europe approving the reimbursement of Xadago(R) (safinamide) for PD patients. Patients in Belgium will now have access to an innovative add-on treatment option that has shown meaningful and long lasting improvements on motor symptoms and good ON Time without troublesome dyskinesia, in addition to a well-tolerated profile".
About Xadago(R) (safinamide)
Safinamide is a new chemical entity with a unique mode of action including selective and reversible MAO-B-inhibition and blocking of voltage dependent sodium channels which leads to modulation of abnormal glutamate release. Clinical trials have established its efficacy in controlling motor symptoms and motor complications in the short term, maintaining this effect over 2 years. Results from 24 month double-blind controlled studies suggest that safinamide shows statistically significant effects on motor fluctuations (ON/OFF time) without increasing the risk of developing troublesome dyskinesia. This effect may be related to its dual mechanism acting on both the dopaminergic and the glutamatergic pathways. Safinamide is a once-daily dose and has no diet restrictions due to its high MAO-B/MAO-A selectivity. Zambon has the rights to develop and commercialize Xadago(R) globally, excluding Japan and other key territories where Meiji Seika has the rights to develop and commercialize the compound. The rights to develop and commercialize Xadago(R) in the USA have been granted to US WorldMeds, by Zambon.
References: Two-year, randomized, controlled study of safinamide as add-on to levodopa in mid to late Parkinson's disease Borgohain, Rupam; Szasz, Jozsef; Stanzione, Paolo; Meshram, Chandrashekhar; Bhatt, Mohit H et al. (2014) Movement disorders : official journal of the Movement Disorder Society vol. 29 (10) p. 1273-80 Anand R: Safinamide is associated with clinically important improvement in motor symptoms in fluctuating PD patients as add-on to levodopa (SETTLE). 17th International Congress of Parkinson's Disease and Movement Disorders, Sydney, Australia, June 16-20, 2013
About Parkinson's disease PD is the second most common chronic progressive neurodegenerative disorder in the elderly after Alzheimer's disease, affecting 1-2% of individuals aged >= 65 years worldwide. The prevalence of the PD market is expected to grow in the next years due to the increase in the global population and advancements in healthcare that contribute to an aging population at increased risk for PD. The diagnosis of PD is mainly based on observational criteria of muscular rigidity, resting tremor, or postural instability in combination with bradykinesia. As the disease progresses, symptoms become more severe. Early-stage patients are more easily managed on L-dopa. L-dopa remains as the most effective treatment for PD, and over 75% of the patients with PD receive L-dopa. However, long term treatment with L-dopa leads to seriously debilitating motor fluctuations, i.e. phases of normal functioning (ON-time) and decreased functioning (OFF-time). Furthermore, as a result of the use of high doses of L-dopa with increasing severity of the disease, many patients experience involuntary movements known as L-dopa-Induced Dyskinesia (LID). As the disease progresses, more drugs are used as an add-on to what the patient already takes, and the focus is to treat symptoms while managing LID and the "off-time" effects of L-dopa. Most current therapies target the dopaminergic system that is implicated in the pathogenesis of PD, and most current treatments act by increasing dopaminergic transmission that leads to amelioration of motor symptoms.
References: BMC Oertel. European Handbook of Neurological Management, Vol1, Chapter 14 & 15, 2011 NICE PD guideline, 2006
About Zambon Zambon is a leading Italian pharmaceutical and fine-chemical multinational company that has earned a strong reputation over the years for high quality products and services. Zambon is well-established in 3 therapeutic areas: respiratory, pain and woman care, and is very strongly committed to its entry into the CNS space. Zambon SpA produces high quality products thanks to the management of the whole production chain which involves Zach (Zambon chemical), a privileged partner for API, custom synthesis and generic products. The Group is strongly working on the treatment of the chronic respiratory diseases as asthma and BPCO and on the CNS therapeutic area with Xadago(R) (safinamide) for the Parkinson treatment. Zambon is headquartered in Milan and was established in 1906 in Vicenza. Zambon is present in 19 countries with subsidiaries and almost 2,700 employees with manufacturing units in Italy, Switzerland, France, China and Brazil. Zambon products are commercialized in 84 countries. For details on Zambon please see: www.zambongroup.com
About Newron Pharmaceuticals Newron (SIX: NWRN) is a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central nervous system (CNS) and pain. The Company is headquartered in Bresso near Milan, Italy. In addition to Xadago(R) for Parkinson's disease, Newron has a strong pipeline of promising treatments for rare disease patients at various stages of clinical development. For more information, please visit: www.newron.com
Further Information
Media Investors and Analysts Zambon Newron Luca Primavera - CCO Stefan Weber - CEO Phone: +39 02 66524491 Phone: +39 02 6103 46 30 Mobile: +39 335 7247417 E-mail: ir@newron.com Email: luca.primavera@zambongroup.com
Italy Milva Naguib Phone: +39 02 66524095 Mobile: +39 3459215675 Email: milva.naguib@zambongroup.com
Belgium Erik LenaersWeber Shandwick Phone: +32 2 894 90 Email: elenaers@webershandwick.com
Newron Stefan Weber - CEO Phone: +39 02 6103 46 30 E-mail: ir@newron.com
UK/Europe Julia Phillips FTI Consulting Phone: +44 (0)20 3727 1000
Switzerland Martin Meier-Pfister IRF Communications Phone: +41 43 244 81 40
Germany Germany Anne Hennecke Anne Hennecke MC Services AG MC Services AG Phone: +49 211 52925222 Phone: +49 211 52925222 anne.hennecke@mc-services.eu anne.hennecke@mc- services.eu U.S. Alison Chen U.S. LaVoieHealthScience Beth Kurth Phone: +1 617 374 8800, Ext. 104 LaVoieHealthScience achen@lavoiehealthscience.com Phone: +1 617 374 8800, Ext. 109 bkurth@lavoiehealthscienc e.com
Important Notices
This document contains forward-looking statements, including (without limitation) about (1) Newron's ability to develop and expand its business, successfully complete development of its current product candidates and current and future collaborations for the development and commercialisation of its product candidates and reduce costs (including staff costs), (2) the market for drugs to treat CNS diseases and pain conditions, (3) Newron's anticipated future revenues, capital expenditures and financial resources, and (4) assumptions underlying any such statements. In some cases these statements and assumptions can be identified by the fact that they use words such as "will", "anticipate", "estimate", "expect", "project", "intend", "plan", "believe", "target", and other words and terms of similar meaning. All statements, other than historical facts, contained herein regarding Newron's strategy, goals, plans, future financial position, projected revenues and costs and prospects are forward-looking statements.
By their very nature, such statements and assumptions involve inherent risks and uncertainties, both general and specific, and risks exist that predictions, forecasts, projections and other outcomes described, assumed or implied therein will not be achieved. Future events and actual results could differ materially from those set out in, contemplated by or underlying the forward-looking statements due to a number of important factors. These factors include (without limitation) (1) uncertainties in the discovery, development or marketing of products, including without limitation negative results of clinical trials or research projects or unexpected side effects, (2) delay or inability in obtaining regulatory approvals or bringing products to market, (3) future market acceptance of products, (4) loss of or inability to obtain adequate protection for intellectual property rights, (5) inability to raise additional funds, (6) success of existing and entry into future collaborations and licensing agreements, (7) litigation, (8) loss of key executive or other employees, (9) adverse publicity and news coverage, and (10) competition, regulatory, legislative and judicial developments or changes in market and/or overall economic conditions.
Newron may not actually achieve the plans, intentions or expectations disclosed in forward-looking statements and assumptions underlying any such statements may prove wrong. Investors should therefore not place undue reliance on them. There can be no assurance that actual results of Newron's research programmes, development activities, commercialisation plans, collaborations and operations will not differ materially from the expectations set out in such forward-looking statements or underlying assumptions.
Newron does not undertake any obligation to publicly up-date or revise forward looking statements except as may be required by applicable regulations of the SIX Swiss Exchange where the shares of Newron are listed.
This document does not contain or constitute an offer or invitation to purchase or subscribe for any securities of Newron and no part of it shall form the basis of or be relied upon in connection with any contract or commitment whatsoever.
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04.04.2016 Dissemination of a Corporate News, transmitted by DGAP - a service of EQS Group AG. The issuer is solely responsible for the content of this announcement.
The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases. Media archive at www.dgap-medientreff.de and www.dgap.de
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450797 04.04.2016
DGAP-News: Newron Pharmaceuticals S.p.A. / Key word(s): Product Launch
Newron Pharmaceuticals S.p.A.: ZAMBON LAUNCHES XADAGO(R) (SAFINAMIDE) IN
BELGIUM FOR PATIENTS WITH MID-TO LATE STAGE PARKINSON'S DISEASE
04.04.2016 / 07:00
The issuer is solely responsible for the content of this announcement.
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ZAMBON LAUNCHES XADAGO(R) (SAFINAMIDE) IN BELGIUM FOR PATIENTS WITH MID-TO
LATE STAGE PARKINSON'S DISEASE
- Zambon today announces the availability and reimbursement in Belgium of
Xadago(R) (safinamide) as an add-on to levodopa alone or in combination
with other Parkinson's disease (PD) medications in mid-to late stage PD
- Safinamide is a new chemical entity with a dopaminergic and non dopaminergic action, providing a balanced control of motor symptoms and motor complications
Milan, Italy - April 4, 2016 - Zambon S.p.A., an international pharmaceutical company strongly committed to the central nervous system (CNS) therapeutic area, and its partner Newron Pharmaceuticals S.p.A. ("Newron") (SIX: NWRN), a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central nervous system (CNS) and pain, today announced the launch of Xadago(R) (safinamide) in Belgium for the treatment of mid- to late stage Parkinson's disease (PD). Following the launch in Switzerland, Germany, Spain and Italy, Xadago(R) (safinamide) is now available in Belgium as add-on therapy to a stable dose of levodopa (L-dopa) alone or in combination with other PD therapies for mid-to late-stage fluctuating patients.
Safinamide is a new chemical entity with a dopaminergic and non-dopaminergic action, providing a balanced control of motor symptoms and motor complications.
Prof. Patrick Santens, from University Hospital Ghent commented: "Thanks to its unique dual dopaminergic and non-dopaminergic mode of action, including the modulation of altered glutamatergic neurotransmission, Xadago(R) (safinamide) has the potential to become a long awaited treatment alternative for our patients suffering from idiopathic Parkinson's disease with motor fluctuations".
Maurizio Castorina, CEO of Zambon SpA said: "We are glad to see health authorities across Europe approving the reimbursement of Xadago(R) (safinamide) for PD patients. Patients in Belgium will now have access to an innovative add-on treatment option that has shown meaningful and long lasting improvements on motor symptoms and good ON Time without troublesome dyskinesia, in addition to a well-tolerated profile".
About Xadago(R) (safinamide)
Safinamide is a new chemical entity with a unique mode of action including selective and reversible MAO-B-inhibition and blocking of voltage dependent sodium channels which leads to modulation of abnormal glutamate release. Clinical trials have established its efficacy in controlling motor symptoms and motor complications in the short term, maintaining this effect over 2 years. Results from 24 month double-blind controlled studies suggest that safinamide shows statistically significant effects on motor fluctuations (ON/OFF time) without increasing the risk of developing troublesome dyskinesia. This effect may be related to its dual mechanism acting on both the dopaminergic and the glutamatergic pathways. Safinamide is a once-daily dose and has no diet restrictions due to its high MAO-B/MAO-A selectivity. Zambon has the rights to develop and commercialize Xadago(R) globally, excluding Japan and other key territories where Meiji Seika has the rights to develop and commercialize the compound. The rights to develop and commercialize Xadago(R) in the USA have been granted to US WorldMeds, by Zambon.
References: Two-year, randomized, controlled study of safinamide as add-on to levodopa in mid to late Parkinson's disease Borgohain, Rupam; Szasz, Jozsef; Stanzione, Paolo; Meshram, Chandrashekhar; Bhatt, Mohit H et al. (2014) Movement disorders : official journal of the Movement Disorder Society vol. 29 (10) p. 1273-80 Anand R: Safinamide is associated with clinically important improvement in motor symptoms in fluctuating PD patients as add-on to levodopa (SETTLE). 17th International Congress of Parkinson's Disease and Movement Disorders, Sydney, Australia, June 16-20, 2013
About Parkinson's disease PD is the second most common chronic progressive neurodegenerative disorder in the elderly after Alzheimer's disease, affecting 1-2% of individuals aged >= 65 years worldwide. The prevalence of the PD market is expected to grow in the next years due to the increase in the global population and advancements in healthcare that contribute to an aging population at increased risk for PD. The diagnosis of PD is mainly based on observational criteria of muscular rigidity, resting tremor, or postural instability in combination with bradykinesia. As the disease progresses, symptoms become more severe. Early-stage patients are more easily managed on L-dopa. L-dopa remains as the most effective treatment for PD, and over 75% of the patients with PD receive L-dopa. However, long term treatment with L-dopa leads to seriously debilitating motor fluctuations, i.e. phases of normal functioning (ON-time) and decreased functioning (OFF-time). Furthermore, as a result of the use of high doses of L-dopa with increasing severity of the disease, many patients experience involuntary movements known as L-dopa-Induced Dyskinesia (LID). As the disease progresses, more drugs are used as an add-on to what the patient already takes, and the focus is to treat symptoms while managing LID and the "off-time" effects of L-dopa. Most current therapies target the dopaminergic system that is implicated in the pathogenesis of PD, and most current treatments act by increasing dopaminergic transmission that leads to amelioration of motor symptoms.
References: BMC Oertel. European Handbook of Neurological Management, Vol1, Chapter 14 & 15, 2011 NICE PD guideline, 2006
About Zambon Zambon is a leading Italian pharmaceutical and fine-chemical multinational company that has earned a strong reputation over the years for high quality products and services. Zambon is well-established in 3 therapeutic areas: respiratory, pain and woman care, and is very strongly committed to its entry into the CNS space. Zambon SpA produces high quality products thanks to the management of the whole production chain which involves Zach (Zambon chemical), a privileged partner for API, custom synthesis and generic products. The Group is strongly working on the treatment of the chronic respiratory diseases as asthma and BPCO and on the CNS therapeutic area with Xadago(R) (safinamide) for the Parkinson treatment. Zambon is headquartered in Milan and was established in 1906 in Vicenza. Zambon is present in 19 countries with subsidiaries and almost 2,700 employees with manufacturing units in Italy, Switzerland, France, China and Brazil. Zambon products are commercialized in 84 countries. For details on Zambon please see: www.zambongroup.com
About Newron Pharmaceuticals Newron (SIX: NWRN) is a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central nervous system (CNS) and pain. The Company is headquartered in Bresso near Milan, Italy. In addition to Xadago(R) for Parkinson's disease, Newron has a strong pipeline of promising treatments for rare disease patients at various stages of clinical development. For more information, please visit: www.newron.com
Further Information
Media Investors and Analysts Zambon Newron Luca Primavera - CCO Stefan Weber - CEO Phone: +39 02 66524491 Phone: +39 02 6103 46 30 Mobile: +39 335 7247417 E-mail: ir@newron.com Email: luca.primavera@zambongroup.com
Italy Milva Naguib Phone: +39 02 66524095 Mobile: +39 3459215675 Email: milva.naguib@zambongroup.com
Belgium Erik LenaersWeber Shandwick Phone: +32 2 894 90 Email: elenaers@webershandwick.com
Newron Stefan Weber - CEO Phone: +39 02 6103 46 30 E-mail: ir@newron.com
UK/Europe Julia Phillips FTI Consulting Phone: +44 (0)20 3727 1000
Switzerland Martin Meier-Pfister IRF Communications Phone: +41 43 244 81 40
Germany Germany Anne Hennecke Anne Hennecke MC Services AG MC Services AG Phone: +49 211 52925222 Phone: +49 211 52925222 anne.hennecke@mc-services.eu anne.hennecke@mc- services.eu U.S. Alison Chen U.S. LaVoieHealthScience Beth Kurth Phone: +1 617 374 8800, Ext. 104 LaVoieHealthScience achen@lavoiehealthscience.com Phone: +1 617 374 8800, Ext. 109 bkurth@lavoiehealthscienc e.com
Important Notices
This document contains forward-looking statements, including (without limitation) about (1) Newron's ability to develop and expand its business, successfully complete development of its current product candidates and current and future collaborations for the development and commercialisation of its product candidates and reduce costs (including staff costs), (2) the market for drugs to treat CNS diseases and pain conditions, (3) Newron's anticipated future revenues, capital expenditures and financial resources, and (4) assumptions underlying any such statements. In some cases these statements and assumptions can be identified by the fact that they use words such as "will", "anticipate", "estimate", "expect", "project", "intend", "plan", "believe", "target", and other words and terms of similar meaning. All statements, other than historical facts, contained herein regarding Newron's strategy, goals, plans, future financial position, projected revenues and costs and prospects are forward-looking statements.
By their very nature, such statements and assumptions involve inherent risks and uncertainties, both general and specific, and risks exist that predictions, forecasts, projections and other outcomes described, assumed or implied therein will not be achieved. Future events and actual results could differ materially from those set out in, contemplated by or underlying the forward-looking statements due to a number of important factors. These factors include (without limitation) (1) uncertainties in the discovery, development or marketing of products, including without limitation negative results of clinical trials or research projects or unexpected side effects, (2) delay or inability in obtaining regulatory approvals or bringing products to market, (3) future market acceptance of products, (4) loss of or inability to obtain adequate protection for intellectual property rights, (5) inability to raise additional funds, (6) success of existing and entry into future collaborations and licensing agreements, (7) litigation, (8) loss of key executive or other employees, (9) adverse publicity and news coverage, and (10) competition, regulatory, legislative and judicial developments or changes in market and/or overall economic conditions.
Newron may not actually achieve the plans, intentions or expectations disclosed in forward-looking statements and assumptions underlying any such statements may prove wrong. Investors should therefore not place undue reliance on them. There can be no assurance that actual results of Newron's research programmes, development activities, commercialisation plans, collaborations and operations will not differ materially from the expectations set out in such forward-looking statements or underlying assumptions.
Newron does not undertake any obligation to publicly up-date or revise forward looking statements except as may be required by applicable regulations of the SIX Swiss Exchange where the shares of Newron are listed.
This document does not contain or constitute an offer or invitation to purchase or subscribe for any securities of Newron and no part of it shall form the basis of or be relied upon in connection with any contract or commitment whatsoever.
---------------------------------------------------------------------------
04.04.2016 Dissemination of a Corporate News, transmitted by DGAP - a service of EQS Group AG. The issuer is solely responsible for the content of this announcement.
The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases. Media archive at www.dgap-medientreff.de and www.dgap.de
---------------------------------------------------------------------------
450797 04.04.2016
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