NEWRON PHARMA N
NEWRON PHARMA N
- CHF (-)
- 15 min delayed data - Switzerland SWX Stocks
Open: -
Change: -
Volume: -
Low: -
High: -
High / Low range: -
Type: Stocks
Ticker: NWRN
ISIN: IT0004147952

DGAP-News: Newron Expands Global Rett Syndrome Burden of Illness Survey Outreach to Europe and Australia

  • 80

DGAP-News: Newron Pharmaceuticals S.p.A. / Key word(s): Miscellaneous/Study
Newron Expands Global Rett Syndrome Burden of Illness Survey Outreach to Europe and Australia

17.02.2020 / 07:00
The issuer is solely responsible for the content of this announcement.


Newron Expands Global Rett Syndrome Burden of Illness Survey Outreach to Europe and Australia

Today's expansion, in close collaboration with Rett advocacy community,
represents the largest, most comprehensive qualitative study ever to examine the burden of Rett syndrome on individuals and their caregivers

Milan, Italy and Morristown, NJ, USA, Feb. 17, 2020 -- Newron Pharmaceuticals S.p.A. ("Newron") (SIX: NWRN, XETRA: NP5), a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central and peripheral nervous system, as part of its commitment to finding a treatment for the symptoms of Rett syndrome, is partnering with the global Rett patient advocacy community to sponsor the first-ever International Rett syndrome Burden of Illness (BOI) survey, to take place in Europe and Australia.

Rett syndrome is a severe neuro-developmental orphan disease with no approved treatment options and overwhelmingly affects girls starting at a very young age. The survey outreach was initially launched in the United States in November 2019 and has achieved strong participation among Rett patient caregivers and medical professionals.

The Burden of Illness survey outreach will launch outside the U.S. today in the UK, Germany, Italy and Australia under the banner "Voices of Rett," and aims to deliver data and analytics to quantify the physical, emotional and financial challenges of Rett syndrome on patients, their families, caregivers and the entire Rett patient community. The results will help identify and guide improved intervention programs and services to complement the Rett care pathway. For the first time ever, an estimate will be made on the economic impact of a disease on a country, its specific regions, its communities, and even individuals. As new advances in Rett are developed, this knowledge and substantiation will help policy makers and the community support the direct and indirect expenditures needed for the treatment and management of Rett patients.

"We are very happy to be able to expand the outreach for our Burden of Illness survey on an international level," said Stefan Weber, CEO of Newron Pharmaceuticals. "We are grateful that this study is strongly supported by so many Rett patient advocacy groups."

"Very little information concerning the true cost of Rett syndrome is available," said Rachael Stevenson, Executive Director of Reverse Rett (UK). "As new advances in treatments for Rett are developed, the community urgently needs this information to support the case for funding."

"The Rett syndrome BOI survey provides a great opportunity for families to help focus the spotlight on the devastating impact of the disorder on the person they love, but also on the impact it has on the whole family," added Becky Jenner, CEO of Rett UK. "With no dedicated treatment for any aspect of Rett syndrome, the study will help the whole community understand just why a treatment, even if it helps with just one symptom, is so very important."

"The survey is key so we can capture and publish individual caregiving situations for the very first time," said Gabriele Keßler, First Chairman of the Federal Association, Rett Deutschland e.V. "Care for these patients often depends heavily on whether the parents have the wherewithal to advocate for the rights of the child with Rett syndrome."

"Even some of our treating physicians have a different view than the families on how Rett syndrome can impact our children's lives and their daily needs," explained Orietta Mariotti, Advisor, ProRETT Ricerca in Italy. "The BOI survey will help bridge this gap to support the needs of Rett children and their families around the globe."

"Australian families can contribute significantly to this large international study to better understand the physical, emotional and financial impacts of Rett syndrome," said Dr. Jenny Downs, Head of Child Disability Health and Wellbeing for the Telethon Kids Institute in Australia. "This will provide critical information to guide how researchers, professionals and agencies, as well as industries work to find new supports and therapies for our children."

"There is a need for a strong family voice to describe the impacts of Rett syndrome symptoms on our families," said Claude Buda, President of Rett Syndrome Association of Austrailia. "This study will build community, professional, NDIS and government knowledge of the most needed supports necessary to live daily with Rett syndrome in Australia."

The International BOI Survey is being conducted by an independent, international Clinical Research Organization in collaboration with Rett syndrome advocacy groups worldwide, along with an advisory panel of experts comprised of physicians, caregivers, advocacy representatives and academic researchers. A scientific poster on the design of this groundbreaking study has been presented at the 26th Annual Conference of the International Society for Quality of Life Research (ISOQOL) in San Diego, CA on October 22, 2019. The final results of this international survey will be published in academic journals to help increase awareness of the burden of illness for Rett syndrome.

Those eligible to participate in the survey include current primary caregivers (including parents, grandparents, siblings, and paid caregivers) of at least one girl/woman with Rett syndrome who is being cared for at least 10 hours per week; and healthcare providers (including physicians, nurses and allied healthcare professionals) who have treated at least three individuals with Rett syndrome in the past five years as part of their practice. Caregivers and healthcare providers seeking to participate in the Survey are encouraged to visit https://voicesofrett.org/ and look for the flag for your specific country at the top, right of the home page.

Newron Pharmaceuticals is developing a treatment to improve the daytime breathing complications, or apneas and their associated impact on overall symptoms of Rett syndrome patients. Apneas are a particularly debilitating core symptom of Rett syndrome, present in approximately 70 percent of patients, and contribute significantly to other co-morbidities, as well as to a reduced quality of life. Newron's pivotal STARS clinical study (Sarizotan Treatment of Apneas in Rett Syndrome) in patients with Rett syndrome has completed enrollment and Newron expects to report results from the STARS study during the first half of 2020.

About Rett Syndrome
Rett syndrome is a severe neurodevelopmental disorder primarily affecting females, with an estimated prevalence of one in 10,000 females. There are no approved treatments available. Rett syndrome is characterized by a loss of acquired fine and gross motor skills and the development of neurological, cognitive and autonomic dysfunction, which leads to loss of ability to conduct daily life activities, walk or communicate. Rett syndrome also is associated with a reduced life expectancy. Approximately 25 percent of the deaths in patients with Rett syndrome are possibly related to multiple cardio-respiratory dysrhythmias that result from brain stem immaturity and autonomic failure. More than 95 percent of these patients have a random mutation in the MeCP2 gene. Episodes of apnea, hyperventilation and disordered breathing are found in approximately 70 percent of patients with Rett syndrome at some stage of their life. For more information on Rett syndrome, visit https://www.rett.de/de/.

STARS Study
Newron has successfully completed patient enrollment in the Sarizotan Treatment of Apneas in Rett Syndrome (STARS) study, a clinical study to evaluate the efficacy, safety and tolerability of sarizotan in patients with Rett syndrome suffering from respiratory symptoms. Among the core symptoms of Rett, breathing disturbances may affect the whole person body; they can have a marked effect on biochemistry, influence emotions, circulation and digestive function as well as musculoskeletal structures in the respiratory process.

About Newron Pharmaceuticals
Newron (SIX: NWRN, XETRA: NP5) is a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central and peripheral nervous system. The Company is headquartered in Bresso near Milan, Italy. Xadago(R)/safinamide has received marketing authorization for the treatment of Parkinson's disease in the European Union, Switzerland, the USA, Australia, Canada, Brazil, Colombia, the United Arab Emirates and Japan, and is commercialized by Newron's Partner Zambon. US WorldMeds holds the commercialization rights in the USA. Meiji Seika has the rights to develop and commercialize the compound in Japan and other key Asian territories. In addition to Xadago(R)/safinamide for Parkinson's disease, Newron has a strong pipeline of promising treatments for rare disease patients at various stages of clinical development, including sarizotan for patients with Rett syndrome and ralfinamide for patients with specific rare pain indications. Newron is also developing Evenamide as the potential first add-on therapy for the treatment of patients with positive symptoms of schizophrenia. For more information, please visit: www.newron.com



For more information
Newron
Stefan Weber - CEO
+39 02 6103 46 26
[email protected]

UK/Europe
Simon Conway / Natalie Garland-Collins, FTI Consulting
+44 20 3727 1000
[email protected]

Switzerland
Martin Meier-Pfister, IRF
+41 43 244 81 40
[email protected]

Germany/Europe
Anne Hennecke, MC Services
+49 211 52925222
[email protected]

USA
Paul Sagan, LaVoieHealthScience
+1 617 374 8800, Ext. 112
[email protected]


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, the timing of commencement of various clinical trials and receipt of data and current and future collaborations for the development and commercialization of its product candidates, (2) the market for drugs to treat CNS diseases and pain conditions, (3) Newron's 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 difficulties in enrolling clinical trials, 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 programs, development activities, commercialization 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.


###
 



17.02.2020 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.
Archive at www.dgap.de


976421  17.02.2020 

fncls.ssp?fn=show_t_gif&application_id=976421&application_name=news&site_id=centralchart
EQS Group
EQS Group

EQS Group is a leading international technology provider for Digital Investor Relations, Corporate Communications and Compliance. More than 8,000 companies worldwide trust EQS’s products and services to securely, efficiently, and simultaneously fulfil complex national and international disclosure and compliance requirements, and to reach stakeholders globally.