Le Lézard
Classified in: Health, Science and technology
Subject: FDA

US FDA grants VICO Therapeutics Orphan-Drug Designation for VO659, an Investigational Therapy for Huntington Disease

LEIDEN, The Netherlands, July 29, 2021 /PRNewswire/ --  VICO Therapeutics, a Leiden Bio Science Park, the Netherlands, based biotech company focusing on the development of RNA modulating therapies for rare neurological disorders, today announced that the Office of Orphan Products Development (OOPD) of the U.S. Food and Drug Administration (FDA) has granted orphan-drug designation for VO659, VICO's investigational antisense oligonucleotide (AON) therapy, for the treatment of Huntington's disease (HD). This news comes only one month after VICO announced that VO659 had received orphan-drug designation for the treatment of spinocerebellar ataxia (SCA). This new designation completes the quartet of orphan designations for VO659 in HD and SCA in both the US and EU.

Vico Therapeutics Logo

Rupert Sandbrink, MD PhD, Chief Medical Officer at VICO, stated: 

"Huntington's disease, like many types of SCA, belongs to the group of polyglutamine disorders which are rare genetic and progressive brain diseases. Patients affected by Huntington's disease experience motor disturbances, personality changes and dementia, leading to increasing disability, loss of independence and reduced survival. Only very limited, symptomatic treatment options are currently available for patients with this devastating disease. Our investigational RNA modulating therapy is aimed to be a disease modifying treatment for polyglutamine disorders, designed to lower the mutant polyglutamine protein levels that cause these neurodegenerative diseases."

"We are delighted that FDA has granted this orphan-drug designation, following the ODD for SCA one month ago. This is affirmation of the potential of our AON approach."

The FDA's Office of Orphan Products Development grants Orphan Drug Designation to drugs and biologics that are defined as those intended for the safe and effective treatment, diagnosis or prevention of rare diseases/disorders that affect fewer than 200,000 people in the U.S. The designation allows VICO to qualify for a number of incentives, including seven years of market exclusivity upon regulatory approval; exemption from FDA application fees for Huntington's Disease; and tax credits for qualified clinical trials.

About Huntington's Disease

Huntington's disease (HD) is a rare inherited neurodegenerative disorder for which there are currently no effective therapeutics. The disease has a wide variation in onset age, with an average age at onset of mid adulthood. This neurodegenerative disorder has a progressive and fatal course characterized by movement disorders, cognitive impairment, dementia and psychiatric manifestations including depression and psychosis. Prevalence is an estimated 4-10 per 100,000 population.

These symptoms result from the selective death and dysfunction of specific neuronal subpopulations within the central nervous system. The disease-causing mutation is the expansion of a CAG-trinucleotide repeat in the coding region of exon 1 of the HTT gene, which results in a mutant huntingtin protein with an elongated polyglutamine (polyQ) stretch at its N-terminus. This expanded polyglutamine stretch confers a toxic gain-of-function to mutant protein forms, ultimately resulting in widespread neuronal death.

About VO659

VICO's lead antisense oligonucleotide product, VO659 is designed to suppress mutant proteins and slow or halt disease progression. A major strength of VICO's approach is the broad applicability to different polyQ diseases and the preferential reduction of mutant relative to normal polyQ proteins.

About VICO Therapeutics

VICO Therapeutics is a Leiden, the Netherlands, based private biotech company focusing on the development of RNA modulating therapies for rare severe neurological disorders. VICO's antisense oligonucleotide platform (AON) is focusing on different forms of spinocerebellar ataxia (SCA) and Huntington Disease (HD). Its early discovery RNA editing platform is directed towards RETT syndrome.


VICO Therapeutics B.V.

Gertjan Bartlema, Chief Executive Officer
T: +31 (0)71 203 68 31
E: Gertjan.bartlema@vicotx.com  

LifeSpring Life Sciences Communication, Amsterdam, the Netherlands
Leon Melens
T: +31 6 538 16 427
E: lmelens@lifespring.nl


SOURCE Vico Therapeutics

These press releases may also interest you

at 14:10
Digi International, , a leading global provider of Internet of Things (IoT) connectivity products and services, today launched my.digi.com, its new twin portals for customer and partner resources. With real-time support, my.digi.com offers a...

at 14:06
Hudl, a leading sports performance analysis company, and WeCOACH, the premier membership organization dedicated to the retention and advancement of women coaches, announced they will be hosting the third-annual BreakThrough Summit. The Summit,...

at 14:05
Clinical logistics and life science manufacturing leaders Boston Labs and Germfree Laboratories Inc. today announced their partnership to launch a new network of mobile CGT manufacturing facilities. The two companies are combining deep logistics, CGT...

at 14:05
delaPlex announced today the availability of a new Center of Excellence (CoE) service to bring together niche expertise and highly skilled technical resources for the advancement of digital transformation in warehouse management (WMS)....

at 14:00
According to Technavio, incremental growth of $ 68.96 mn is expected in the high-altitude pseudo satellites (HAPS) market during 2021-2025. The report offers a detailed analysis of the impact of the COVID-19 pandemic on the high-altitude pseudo...

at 14:00
The "Philippines Data Center Market - Investment Analysis & Growth Opportunities 2021-2026" report has been added to ResearchAndMarkets.com's offering. Philippines data center market size will witness investments of USD 535 million by 2026, growing...

News published on 29 july 2021 at 02:57 and distributed by: