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2014 Product Catalog!

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Wall Charts

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Hematologic Malignancy Testing Algorithm

Clonality Testing Strategy

 

 

Notice: Acute Myeloid Leukemia (AML) The FDA has made it clear that a FLT3 companion diagnostic is required for approval of any FLT3-targeted or FLT3-stratified therapy. LabPMM is the only clinical laboratory with access to the patents required to develop and offer a FLT3 companion diagnostic for worldwide use.


Personalized Medicine & IVS
Invivoscribe is a leading provider of clinically-validated CE-marked in vitro diagnostic products. Through our subsidiary, LabPMM, we provide worldwide access to molecular biomarker testing, which enables pharmaceutical companies to bring to the market new targeted treatments, and allows physicians to better determine optimal treatment for their patients.

Research & Biotechnology
Development & Partnering
Companion Diagnostics

View a video of our AMP 2013 Workshop!

We have posted a condensed version of our AMP workshop entitled Clonality Testing by Next-Generation Sequencing: Latest Developments from the New Frontier. This talk was given to a capacity audience in Phoenix, AZ in November 2013, and now you can enjoy highlights at your own convenience. Click here to view.

 

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LymphoTrack™ IGH Assay Launched

Invivoscribe has expanded its portfolio of next-generation sequencing (NGS) products with the introduction of the LymphoTrack™ IGH Assay (for MiSeq platform). This assay provides unprecedented levels of information in the form of frequency distributions and DNA sequences of rearranged IGH genes. Click here for more information. Contact us to learn more.

 

CAP Today

The Feature Story in the May 2013 issue of CAP Today titled: “Molecular clonality testing for lymphoma” highlights the benefits of PCR-based B and T cell clonality assays from Invivoscribe. Click here to view the article.

 

LabPMM and New York

LabPMM is happy to announce that we have received our New York state clinical lab license. Please contact us with any questions.

 

Invivoscribe Launches the LymphoTrack™ TCRG Assay - MiSeq

This Next Generation Sequencing (NGS) assay provides data for the study of TCRG clonality and provides the frequency distribution and DNA sequence of rearranged TCRG V-J sequences using the MiSeq platform. Click here for more information. Contact us to learn more.

 

Invivoscribe Launches Genection, a New Personalized Molecular Medicine Company Delivering Global Access to the Entire Clinically-Actionable Genetic Menu.

Click here to learn more about Genection.

 

CE-marked TCRG Gene Rearrangement Assay 2.0

This in vitro diagnostic assay, which is available for sale and use only outside North America, detects the vast majority of clonal T cell receptor gamma gene rearrangements with a single multiplex master mix, generates a single Gaussian distribution in a size range consistent with testing FFPE specimens, and comes with software that assists with objective interpretation. Contact us or visit our online catalog to learn more.

 

TCRG Gene Rearrangement Assay 2.0

Our improved assay detects the vast majority of clonal T cell receptor gamma gene rearrangements with a single multiplex master mix, and generates a single Gaussian distribution in a size range consistent with testing FFPE specimens. Contact us or visit our online catalog to learn more.

 

BCR/ABL RNA Dilution Sets are available

We have released our BCR/ABL b3a2, b2a2, and e1a2 RNA Dilution Sets.

Contact us to learn more.

In the News

January 8, 2014

Invivoscribe embraces the value of constant process improvement

 

July 16, 2013 Marketwired

Invivoscribe FLT3 Method Patent Claims Upheld 

 

June 19, 2013 Marketwired
Invivoscribe FLT3 Testing Patents Strengthened by Supreme Court Ruling

 

May 14, 2013 Marketwire
Invivoscribe Prevails in German District Court (FLT3 Patent Infringement Action)

 

December 5, 2012 Marketwire
Takara Bio Grants Patent License to Invivoscribe Technologies for FLT3-ITD Testing in Japan

 

December 4, 2012 Marketwire
Invivoscribe Launches Genection, a New Personalized Molecular Medicine Company Delivering Global Access to the Entire Clinically-Actionable Genetic Test Menu

 

May 15, 2012 USPTO
United States Patent No. 8,178,292 issued on May 15, 2012.  This patent further consolidates our already dominant intellectual property around the detection of FLT3-ITD mutations

 

December 26, 2011 The New York Times
A Push to Tie New Drugs to Testing by Andrew Pollack


February 23, 2011 Pharmacogenomics Reporter
Novartis, Invivoscribe to Develop Companion Test for Acute Myeloid Leukemia Rx Midostaurin


February 21, 2011 BioCentury
Invivoscribe Technologies Inc., Novartis deal


Press Releases
February 15, 2011
Invivoscribe Announces Collaboration Agreement to Develop Companion Diagnostic


Our growth continues... and continues...

We doubled space at our San Diego headquarters in 2011, building out two additional suites for cGMP manufacturing and shipping. In April 2012 we expanded into another adjacent suite to secure offices for management personnel. LabPMM LLC expanded into dedicated space San Diego in 2011, and LabPMM GmbH, located in Martinsried, Germany, started the move into our brand new European reference laboratory in September 2011. Personnel were hired and completed training at our San Diego facility, and we anticipate completion of assay validation and the start of clinical testing in 2Q2012.

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Invivoscribe Companies

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Meetings and Conferences

 

May 31-June 3, 2014
Milano Congressi, Viale Enginardo (Gate 2), Milan, Italy  


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June 13-16, 2014
19th Congress of EHA. Milan, Italy   


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November 12, 2014

Corporate Workshop
AMP 2013 Annual Meeting
National Harbor, MD, USA


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November 13-15, 2014
AMP 2013 Annual Meeting
National Harbor, MD, USA


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December 6-9, 2014
2014 ASH Annual Meeting and Exposition
Moscone Center, San Francisco, CA, USA

   

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