FDA Grants Orphan Drug Designation for Neuren's NNZ-2591 to Treat Angelman, Phelan-McDermid and Pitt Hopkins Syndromes
17 October 2019 - 8:49PM
Business Wire
Neuren Pharmaceuticals (ASX: NEU) today announced that the US
Food and Drug Administration (FDA) has granted Orphan Drug
Designation to Neuren’s NNZ-2591 for the treatment of Angelman
syndrome, Phelan-McDermid syndrome and Pitt Hopkins syndrome.
Neuren Executive Chairman Richard Treagus commented: “Orphan
Drug Designation is an important commercial milestone which adds
significant value and momentum in respect of our plans to move
NNZ-2591 into clinical trials in 2020. This confirms that NNZ-2591
is a valuable asset for Neuren and validates the encouraging
preclinical data as well as our plans to develop NNZ-2591 in
parallel for these three debilitating childhood disorders with
urgent unmet need. We look forward to working with the FDA as we
execute on our development plans.”
Neuren previously announced positive results for NNZ-2591 in
separate mouse models for Phelan-McDermid syndrome, Angelman
syndrome and Pitt Hopkins syndrome, three debilitating
neurodevelopmental disorders for which currently there are no
approved drug therapies. Each disorder is caused by a mutation or
deletion in a different gene; however, they share an underlying
impairment in the connections and signaling between brain cells,
which is the target for treatment with NNZ-2591.
Orphan Drug designation is a special status that the FDA may
grant to a drug to treat a rare disease or condition. Amongst other
incentives, Orphan Drug designation qualifies the sponsor of the
drug for 7 years of marketing exclusivity, plus 6 months if
approved for pediatric use, as well as a waiver of the prescription
drug user fee for a marketing application.
- Ends -
Notes to Editors
About Neuren Neuren Pharmaceuticals Limited (Neuren) is a
biopharmaceutical company developing new therapies for
neurodevelopmental disorders with high unmet need, utilizing
synthetic analogs of neurotrophic peptides that occur naturally in
the brain. Neuren completed Phase 2 development of trofinetide for
Rett syndrome and has completed a Phase 2 clinical trial in Fragile
X syndrome. The programs in Rett syndrome and Fragile X syndrome
have each received Fast Track designation by the US Food and Drug
Administration and Orphan Drug designation in both the United
States and the European Union. Neuren has granted an exclusive
license to ACADIA Pharmaceuticals Inc. for the development and
commercialization of trofinetide in North America, whilst retaining
all rights outside North America. Neuren is advancing the
development of its second drug candidate NNZ-2591 for
Phelan-McDermid syndrome, Angelman syndrome and Pitt Hopkins
syndrome.
Find out more about us online at: www.neurenpharma.com
Forward-looking Statements This announcement contains
forward-looking statements that are subject to risks and
uncertainties. Such statements involve known and unknown risks and
important factors that may cause the actual results, performance or
achievements of Neuren to be materially different from the
statements in this announcement.
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version on businesswire.com: https://www.businesswire.com/news/home/20191017005361/en/
At the Company Neuren Pharmaceuticals Limited (Australia)
Jon Pilcher, CFO & Company Secretary Phone: +61 438 422 271
Email: jpilcher@neurenpharma.com
Instinctif Partners (UK/RoW) Melanie Toyne Sewell/ Ashley
Tapp Phone: +44 (0)20 7457 2020 Email:
Neuren@instinctif.com
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