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Eurobio Scientific, the leading French provider of specialty in vitro diagnostics and life-science solutions.

 

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Home » Our Products
 » Portfolio of Proprietary Products
Portfolio of Proprietary Products

 

> Commercialized products

> Exclusive license products

> Co-developped with Partners products

 

 

 

Commercialized products


Tétanos Quick Stick®
(TQS):
Tétanos Quick Stick® (TQS) is able to provide a reliable and rapid assessment, in emergency clinics, to assist in the decision of which personalized anti-tetanus prophylaxis is appropriate. 
Tétanos Quick Stick® (TQS) is a unitary test that allows, within 10 minutes, the determination of the tetanus vaccination status of a patient with an at risk wound. Using TQS avoids hyper-immunization and limits the administration of unnecessary immunoglobulin injections.
 

Our distributors of Tétanos Quick Stick® (TQS): Europe et Asia.

 

 

 For additional information, please contact our Hotline: +33 1 69 79 18 18.

 

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Exclusive license products

 

 

AlloMap®:
AlloMap® is a gene-expression profiling based blood test. The test is a new method for regular and non-invasive surveillance of heart transplant recipients for acute cellular rejection, thereby contributing to patient follow-up optimization. AlloMap provides unique information regarding the body’s immune response to a transplanted heart in the form of an objective score.
 
The test has been clinically validated in four major clinical studies in the US and Europe, involving over 2,000 heart transplant recipients and 40 clinical centers. Surveillance of heart recipients with the non-invasive AlloMap test has been shown to be as effective as surveillance with biopsies in heart transplantation clinical outcomes, based on the landmark IMAGE study published in the New England Journal of Medicine in April 2010.
 
The International Society of Heart and Lung Transplantation recommended AlloMap testing in its guidelines for the management of heart transplant recipients in August 2010.
 
Developed and marketed since 2005 by XDx in the United States as a CLIA certified test, AlloMap was cleared in 2008 by the U.S. Food and Drug Administration through the 510K de novo process, and has gained acceptance by heart transplantation key opinion leaders to aid in the management of their patients as an alternative surveillance method. 2,000 heart transplants are performed annually in the United States in 120 medical centers, and over 90 centers have used AlloMap. To date, more than 10,000 patients have received the test in the United States. The use of AlloMap has extensive reimbursement coverage by both private and government health insurance. The test received CE marking in 2011.
 
Diaxonhit will promote AlloMap in Europe through its wholly owned subsidiary, InGen, the leader in France for marketing tests related to transplantation and histocompatibility testing.
 
1. Pham et al, Gene-Expression Profiling for Rejection Surveillance after Cardiac Transplantation. N Engl J Med 2010;362(20):1890-900.


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Co-developped with Partners products

 

 

TEDAC Consortium:
Headed by project leader ERYTECH Pharma, the consortium includes Diaxonhit, AP-HP (Paris Public Hospitals), Inserm (National Institute for medical research), and Paris-Diderot University. It aims at developing innovative therapies for the enzymatic treatment of chemo- or radio- resistant cancers, and tools enabling personalized care of patients.

 

 

Companion diagnostic for resistant cancers

 

Diaxonhit will be responsible for two phases of the project that utilize its hGWSA technology, which enables the study of the transcriptomic profile of tumors:

1) the identification of biomarkers of susceptibility to therapeutic response in the context of reducing the risks associated with the development of treatments, and
2) the development of an enzymatic therapy companion diagnostic that will identify responders, thus improving personalized care.
 
 
Test  for treatment monitoring 
 
Diaxonhit is also in charge of the development of a test to monitor the direct effect of drug activity by measuring the depletion of amino acids. The test result will allow the clinician to adjust and optimize an individual patient’s therapeutic regiment.
 

 

  

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