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

RogCon and Prometheus Research Enter into Partnership to Support International Natural History Study on SCN2A Mutations

NEW HAVEN, Conn., Jan. 14, 2019 /PRNewswire/ -- RogCon Biosciences, Inc., (RogCon), a biotechnology company leading the discovery and development of novel treatments for patients suffering from SCN2A (Nav1.2) mutations, has partnered with Prometheus Research to support the creation of a scalable clinical data registry (CDR) that will assist a planned international natural history study of patients with SCN2A mutations being conducted by top neurologists and epileptologists around the world, including Dr. Katherine Howell of The Royal Children's Hospital as lead investigator.  Mutations of the SCN2A gene are known to cause several neurological disorders including epilepsy, autism and a number of other neuro-related conditions, affecting tens of thousands of people worldwide.

Prometheus' CDR solution will enable the investigators of this SCN2A natural history study to collect complex data, faciliate multisite protocols, and ultimately aid in understanding the symptomatology associated with SCN2A mutations and how patients progress with their disease over time. At present, there is no corrective therapy or cure specifically for SCN2A patients, and all drugs being used are non-selective treatments that only offer relief for select patient symptoms. The information from the natural history study and the Prometheus CDR will be essential for advancing the current standard of care, and will provide critical aid to the  development of new disease-modifying treatments, such as those currently being pursued by RogCon. 

"We are excited to work with Prometheus on this critical initiative, and to support the immensely-valuable international natural history study on SCN2A mutations," said Alex Nemiroff, CEO and co-founder of RogCon. "The data generated from this study is paramount to the missions of all those seeking to better treat this disease, and at RogCon we acknowledge the value of Prometheus' data platform, technologies, and expertise to help bring a disease-modifying therapy to the many patients and families suffering from SCN2A mutations."

The SCN2A study leverages Prometheus' RexRegistry platform, which includes end-to-end support for data acquisition, curation, enrichment, and analysis. RexRegistry can accommodate changing data standards, information models, and regulatory requirements with minimal technical effort and without affecting the quality or availability of existing data. It is designed to adapt to evolving needs of data stewards and their initiatives by offering multiple channels through which data can be acquired and reused, and by ensuring both the data and the infrastructure itself can remain usable for decades to come.

Prometheus' CEO, Dr. Leon Rozenblit, commented: "We believe the potential for better understanding SCN2A mutations is enormous and our team at Prometheus is delighted that our expertise and technologies will be useful in advancing this critical initiative. We are always excited to help create high-quality data assets that accelerate discovery in a high-impact area, such as neurological diseases, and in particular, SCN2A."

About Prometheus Research
Prometheus Research is the principal informatics partner to organizations engaged in ambitious translational research endeavors and national quality-improvement initiatives. Their research-grade clinical registry solutions leverage open technologies and standards to deliver unparalleled versatility when acquiring data and exceptional quality when analyzing and repurposing data. Prometheus helps forward-thinking health institutions build data assets today that will advance the state of care for future generations.  www.prometheusresearch.com

About RogCon Biosciences
RogCon is a biotechnology company pioneering the discovery and development of novel therapeutics for children suffering from SCN2A mutations, where no solutions currently exist.  Mutations in SCN2A are the most common cause of neurodevelopmental disease including epilepsy and autism, and there are numerous associated comorbidities.  RogCon has amassed a group of world experts in genetic epilepsy research and drug development, with a focus on SCN2A, including collaborations with Ionis Pharmaceuticals, Inc. and The Florey Institute of Neuroscience.  To learn more, please visit www.rogcon.com

SOURCE Prometheus Research

These press releases may also interest you

at 18:04
The global data classification market size to grow at a Compound Annual Growth Rate (CAGR) of 25.4% during the forecast periodRead the full report: https://www.reportlinker.com/p05723877 MarketsandMarkets forecasts the global data classification...

at 18:00
AUSTIN, Texas, Jan. 17, 2019 /PRNewswire-PRWeb/ -- The Austin Business Journal recently released its list of top women-owned businesses and Firefly Consulting, led by President Kimberly Watson-Hemphill, has once again made the cut. In a city that...

at 18:00
The "Telepresence Robot - Global Market Outlook (2017-2026)" report has been added to ResearchAndMarkets.com's offering. Global Telepresence Robot market accounted for $127.72 million in 2017 and is expected to reach $569.80 million by 2026 growing...

at 18:00
CHICAGO, Jan. 17, 2019 /PRNewswire-PRWeb/ -- Otus, a Chicago-based educational technology provider for K-12 school communities, today announced the appointment of Ed Earley as Chief Software Architect. Earley most recently served as Head of...

at 17:40
DALLAS, Jan. 17, 2019 /PRNewswire-PRWeb/ -- DAVACO, the North American leader of high-volume programs for global brands, announced today that DAVACO's ClearThread platform now provides an enhanced experience for monitoring and reviewing program data...

at 17:37
SPS DGTL, the 24x7x365 multilingual digital communications agency, is excited to announce their newest venture; DGTL Local. After five years of operations, SPS DGTL saw a gap and need for local businesses with less than $10 million in annual sales...

News published on 14 january 2019 at 08:15 and distributed by: