Our History, Step-by-Step

June 2011 ISignal Genetics and DiagnoCure enter into a collaboration agreement to commercialize the Previstage™ GCC test.
May 2011

Publication (Annals of Surgical Oncology) of study results supporting the quantitative prognostic value of Previstage™ GCC for stage II colon cancer patients.

September 2010 Filing of a PMA with the FDA for the PCA3 test.
April 2010 In a new study, PCA3 shows good performance before the initial prostate biopsy.
March 2010: Clinical-utility of PCA3 confirmed in two large worldwide studies, conducted on a subset of 2,400 patients in GlaxoSmithKline's REDUCE trial.
August 2009: DiagnoCure's partner, Gen-Probe, begins U.S. clinical study of the PROGENSA® PCA3 assay for prostate cancer aimed at securing FDA approval.
May 2009: DiagnoCure announces completion of an investment of US$5 million by Gen-Probe Incorporated in the Company.
February 2009: Major study on DiagnoCure's GCC biomarker published in the Journal of the American Medical Association.
August 2008: DiagnoCure launches its Previstage™ GCC Colorectal Cancer Staging Test, available through its U.S. CLIA-certified clinical laboratory, DiagnoCure Oncology Laboratories.
August 2007: DiagnoCure acquires Catalyst Oncology and its proprietary prognostic tests based on the measure of the Shc proteins for breast, colon and potentially other cancers.
April 2007: DiagnoCure secures exclusive worldwide rights to two high-value molecular tests based on the detection of GCC for colorectal cancer.
April 2007: Completion of a public offering of common shares for gross proceeds of $25,155,000.
November 2006: Gen-Probe's PCA3 test receives European CE Mark and is launched in six laboratory sites across Europe.
May 2006: DiagnoCure and Gen-Probe expand the terms of their agreement and collaboration for the research of additional applications of the PCA3 gene, and the evaluation of certain lung cancer markers.
March 2006: DiagnoCure’s exclusive rights to PCA3, its highly prostate-cancer specific gene, are confirmed as the United States Patent and Trademark Office (USPTO) grants a patent on the PCA3 gene technology, which encompasses both therapeutic and diagnostic applications.
July 2004: Completion of a public offering of common shares for gross proceeds of $23,750,000.
November 2003: Gen-Probe and DiagnoCure enter into a collaboration agreement for the joint development and commercialization by Gen-Probe of a molecular test for the detection of the PCA3 gene for the diagnosis of prostate cancer.
September 2003: Conclusion of an agreement with Bostwick Laboratories (US) for the supply of our uPM3™ test for prostate cancer in an ASR format.
December 2001: Completion of a public offering of common shares with gross proceeds of $8.625 million.
June 2001: Developed the prostate cancer detection test uPM3™. Set up protocols and performed preliminary clinical studies on more than 200 patients.
May 2000: DiagnoCure acquired from Nijmegen University (The Netherlands) an exclusive worldwide license for all diagnostic and therapeutic applications of the PCA3 gene technology, a specific prostate cancer marker.
March 2000: Clearance by the FDA to commercialize ImmunoCyt™ in the United States.
December 1999: Shares listed on the Toronto Stock Exchange on December 6, 1999.
November 1996: Issue of common shares and warrants on the Montreal Stock Exchange in the course of the Company's initial public offering. The net proceeds amounted to $13.4 million (Can.).
November 1995: Private financing of $6 million (Can.).
December 1994: Incorporation of the Company.