MARLBOROUGH, Mass.--(BUSINESS WIRE)--Sunovion Pharmaceuticals Inc. (Sunovion) today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the resubmission of the New Drug Application for SUN-101/eFlow® (glycopyrrolate) for the long-term, maintenance treatment of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or emphysema.
This resubmission is in response to the Complete Response Letter Sunovion received from the FDA on May 26, 2017. The expected action date by the FDA under the Prescription Drug User Fee Act (PDUFA) is December 15, 2017.
“We look forward to working with the FDA during their review of the SUN-101/eFlow® resubmission, which, if approved, would be the first nebulized LAMA for patients with COPD in the United States,” said Antony Loebel, M.D., Executive Vice President and Chief Medical Officer at Sunovion, Head of Global Clinical Development for Sumitomo Dainippon Pharma Group. “Building on the strength of our heritage in nebulized treatment for COPD, the development of this innovative drug-device combination underscores our commitment to ensuring patients have choices in medication and delivery options with the goals of individualizing and optimizing treatment.”
The NDA for SUN-101/eFlow® is supported by data from clinical trials in the GOLDEN (Glycopyrrolate for Obstructive Lung Disease via Electronic Nebulizer) program, which demonstrated a statistically significant change from baseline in morning pre-dose trough forced expiratory volume in one second (FEV1) versus placebo in addition to safety and tolerability in a long-term study. Sunovion was not required by the FDA to conduct any additional clinical studies prior to NDA resubmission.
About SUN-101/eFlow®
SUN-101
(glycopyrrolate) is a long-acting muscarinic antagonist (LAMA)
bronchodilator delivered via the proprietary investigational eFlow®
closed system nebulizer (PARI Pharma GmbH). SUN-101/eFlow® is
currently in development as a nebulized treatment for patients with
moderate-to-very severe COPD. The investigational combined product,
consisting of SUN-101 and the investigational eFlow® closed
system nebulizer, which has been optimized for SUN-101 delivery, has not
been approved by the FDA for the treatment of COPD.
About COPD
Chronic obstructive pulmonary disease (COPD) is a
common, preventable and treatable disease that is characterized by
persistent respiratory symptoms and airflow limitation that is due to
airway and/or lung abnormalities usually caused by significant exposure
to toxic particles or gases. The main risk factor for COPD is tobacco
smoking, but other environmental exposures may contribute.1 Approximately
15.7 million adults in the U.S. report that they have been diagnosed
with COPD.2 It is estimated that several million more adults
have undiagnosed COPD.3 COPD is responsible for over 120,000
deaths per year, making it the third leading cause of death in the U.S.2
COPD develops slowly and the symptoms often worsen over time,
potentially limiting the ability to perform routine activities.2
Symptoms of COPD include coughing, wheezing, shortness of breath, excess
production of mucus in the lungs, the inability to breathe deeply and
the feeling of being unable to breathe.4 The symptoms of COPD
can be most severe during the night and early morning.5 Morning
symptoms can be associated with limitation of activities during the day,
impaired health status and increased risk of exacerbation.6
Night-time symptoms disturb sleep, reduce sleep quality and, in the long
term, may be associated with development or worsening of cardiovascular
diseases, cognition, depression and increased mortality.7
About Sunovion Pharmaceuticals Inc. (Sunovion)
Sunovion is a
global biopharmaceutical company focused on the innovative application
of science and medicine to help people with serious medical conditions.
Sunovion’s vision is to lead the way to a healthier world. The company’s
spirit of innovation is driven by the conviction that scientific
excellence paired with meaningful advocacy and relevant education can
improve lives. With patients at the center of everything it does,
Sunovion has charted new paths to life-transforming treatments that
reflect ongoing investments in research and development and an
unwavering commitment to support people with psychiatric, neurological
and respiratory conditions. Sunovion’s track record of discovery,
development and/or commercialization of important therapies has included
Utibron™ Neohaler® (indacaterol/glycopyrrolate) inhalation
powder, Brovana® (arformoterol tartrate) inhalation solution,
Latuda® (lurasidone HCI) and Aptiom®
(eslicarbazepine acetate).
Headquartered in Marlborough, Mass., Sunovion is an indirect, wholly-owned subsidiary of Sumitomo Dainippon Pharma Co., Ltd. Sunovion Pharmaceuticals Europe Ltd., based in London, England, and Sunovion Pharmaceuticals Canada Inc., based in Mississauga, Ontario, are wholly-owned direct subsidiaries of Sunovion Pharmaceuticals Inc. Additional information can be found on the company’s web sites: www.sunovion.com, www.sunovion.eu and www.sunovion.ca. Connect with Sunovion on Twitter, LinkedIn, Facebook and YouTube.
About Sumitomo Dainippon Pharma Co., Ltd.
Sumitomo Dainippon
Pharma is among the top-ten listed pharmaceutical companies in Japan
operating globally in major pharmaceutical markets, including Japan, the
United States, China and the European Union. Sumitomo Dainippon Pharma
aims to create innovative pharmaceutical products in the Psychiatry &
Neurology area and the Oncology area, which have been designated as the
focus therapeutic areas. Sumitomo Dainippon Pharma is based on the
merger in 2005 between Dainippon Pharmaceutical Co., Ltd., and Sumitomo
Pharmaceuticals Co., Ltd. Today, Sumitomo Dainippon Pharma has about
6,500 employees worldwide. Additional information about Sumitomo
Dainippon Pharma is available through its corporate website at www.ds-pharma.com.
LATUDA and SUNOVION are registered trademarks of Sumitomo Dainippon
Pharma Co., Ltd.
BROVANA is a registered trademark of Sunovion
Pharmaceuticals Inc.
APTIOM is used under license from Bial.
UTIBRON
is a trademark of Novartis AG, used under license.
NEOHALER is a
registered trademark of Novartis AG, used under license.
eFlow is a
registered trademark of PARI Pharma GmbH.
Sunovion Pharmaceuticals Inc. is a U.S. subsidiary of Sumitomo Dainippon Pharma Co., Ltd.
© 2017 Sunovion Pharmaceuticals Inc. All rights reserved.
For a copy of this release, visit Sunovion’s web site at www.sunovion.com
References
1 GOLD Guidelines 2017. http://www.goldcopd.org/guidelines-global-strategy-for-diagnosis-management.html.
Accessed: March 16, 2017.
2 MMWR: Morbidity and
Mortality Weekly Report. Employment and Activity Limitations Among
Adults with Chronic Obstructive Pulmonary Disease — United States, 2013.
March 27, 2015; 64(11). Available at http://www.cdc.gov/mmwr/
3
National Heart, Lung, and Blood Institute. “What is COPD?” Available at: http://www.nhlbi.nih.gov/health/educational/copd/what-is-copd/index.htm.
Accessed: March 2, 2016
4 National Heart, Lung and Blood
Institute. (2013). What Are the Signs and Symptoms of COPD? Retrieved
from https://www.nhlbi.nih.gov/health/health-topics/topics/copd/signs.
5
Partridge MR, Karlsson N, Small IR. Patient insight into the impact of
chronic obstructive pulmonary disease in the morning: an internet
survey. Curr Med Res Opin. 2009;25:2043–8.
6 Roche N,
Small M, Broomfield S, Higgins V, Pollard R. Real world COPD:
association of morning symptoms with clinical and patient reported
outcomes. COPD. 2013;10:679–86.
7 Agusti A, Hedner J,
Marin JM, Barbé F, Cazzola M, Rennard S. Night-time symptoms: a
forgotten dimension of COPD. Eur Respir Rev. 2011;20:183–94.
