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VIRxSYS Corporation

VIRxSYS Corporation is a privately held biotech company. The Company was founded in 1998 and is located in the biotech corridor of Gaithersburg, Maryland. Using technology first developed by and exclusively licensed from The Johns Hopkins University, VIRxSYS has developed a gene delivery system (a vector) from a human lentivirus for the treatment of serious diseases such as HIV/AIDS and cancer.
With the successful development of numerous genetic and therapeutic payloads, there have been great promises of genetic medicine. However, most of these promises have been unfulfilled because of the medical industry's inability to develop a transport system to deliver the genetic and therapeutic payloads into targeted cells efficiently, reproducibly and permanently.

Today this is no longer an issue, as VIRxSYS has solved this final hurdle that will now allow the promises of genetic medicine to become a reality. Payloads delivered by other vectors previously and currently used have serious drawbacks, while payloads delivered via VIRxSYS' lentiviral vector (i) have staying power within a cell because the payloads become a permanent part of the cell's genetic material, (ii) have a 95%+ delivery efficiently compared to approximately 20% to 50% for other viral vectors, (iii) can reproduce this delivery efficiently under optimal and sub optimal conditions.


Contact Details:
200 Perry Parkway, Suite 1A
Gaithersburg
Maryland
20877
United States of America
Tel:301.987.0480
Fax:
Email:findout@virxsys.com
WWW:

www.virxsys.com/




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Recent Publications by VIRxSYS Corporation:

Lentiviral vectors in clinical trials: Current status.
Lentiviral vectors (LVs) are the most recently developed viral-derived...
7th October, 2009
VIRxSYS Corp, Gaithersburg, MD 20877, USA. Curr Opin Mol Ther. 2009 Oct;11(5):554-64.
Lentiviral vectors for HIV disease prevention and treatment.
HIV/AIDS has posed major challenges to the scientific community, both in...
23rd July, 2009
VIRxSYS Corporation, 200 Perry Parkway, Gaithersburg, MD 20877, United Vaccine. 2009 May 26;27(25-26):3443-9. Epub 2009 Feb 6.
DOI Direct Link
Trans-splicing into highly abundant albumin transcripts for production of therapeutic proteins in vivo.
Spliceosome-mediated RNA trans-splicing has emerged as an exciting mode of...
7th April, 2009
VIRxSYS Corporation, Gaithersburg, Maryland, USA. Mol Ther. 2009 Feb;17(2):343-51. Epub 2008 Dec 9.
DOI Direct Link
Generation of a packaging cell line for prolonged large-scale production of high-titer HIV-1-based lentiviral vector.
BACKGROUND: A stable packaging cell line facilitates large-scale...
27th August, 2005
VIRxSYS Corporation, Gaithersburg, Maryland 20877 [correction] USA. J Gene Med. 2005 Jun;7(6):818-34.
DOI Direct Link
Regulatory considerations for novel gene therapy products: a review of the process leading to the first clinical lentiviral vector.
This review is intended to exemplify the roles and responsibilities of the...
1st June, 2005
VIRxSYS, 200 Perry Parkway, Hum Gene Ther. 2005 Jan;16(1):17-25.
DOI Direct Link

View more VIRxSYS Corporation research publications.

Press Releases on VIRxSYS Corporation:

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VIRxSYS Publishes New Study on RNA Therapy 6th April, 2009 VIRxSYS Corporation
New RNA therapy reversed hemophilia in mice GAITHERSBURG, Md., April 6 /PRNewswire/ -- VIRxSYS Corporation announced today the publication of a new research article, "Trans-splicing into Highly
VIRxSYS to Host a Web Conference to Announce Clinical Trial Update 21st July, 2008 VIRxSYS Corporation
GAITHERSBURG, Md., July 21 /PRNewswire/ -- VIRxSYS Corporation, a privately held company developing gene therapies for HIV and genetic diseases, will present an update on the VRX496 Phase I and

BioNews Results for VIRxSYS Corporation:

VIRxSYS collects $9.8M of $40M round for genetic medicine tech
TechJournal South:  Nov 6 2009 2:05PM Matching: virxsys

VIRxSYS Corporation Patents:

US Patent No.Title
7427474 High-throughput methods for identifying gene function using lentiviral vectors
7399753 Trans-splicing mediated photodynamic therapy
6835568 Regulated nucleic acid expression system
6627442 Methods for stable transduction of cells with hiv-derived viral vectors

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