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Intarcia Supports American Diabetes Association Call For Independent Review Of Incretin-Based Therapies
Date:6/13/2013

BOSTON, June 13, 2013 /PRNewswire/ -- Intarcia Therapeutics, Inc. today announced its support for the American Diabetes Association's (ADA) call for larger, longer-term, and more rigorous datasets and an independent review of pooled data on the safety of incretin-based diabetes medications, including GLP-1 analogs and DDP-4 inhibitors. The ADA made its announcement ahead of this week's NIDDK-NCI Workshop. Intarcia is currently conducting Phase 3 studies of its lead development candidate, ITCA 650, as a once- or twice-yearly treatment for patients with type 2 diabetes. ITCA 650 contains exenatide, a glucagon-like peptide-1 (GLP-1) receptor agonist.

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"Intarcia is an evidence-based company and nothing is more important than the safety of our medicines, transparency of data, and the appropriate and beneficial use of our medicines at every stage of development and once on the market," said Kurt Graves, Chairman, President and CEO of Intarcia. "We fully support the ADA's leadership here, their call to incretin therapy companies for all relevant patient-level data, and bringing their independent expertise to bear on the right questions and the best data to answer them. We are pleased to contribute the data as they become available from our ongoing FREEDOM global Phase 3 program, which is designed to include at least 4,000 patients."

Michelle Baron, MD, FACE, Chief Medical Officer of Intarcia, commented on the ADA announcement as well:  "Intarcia is committed to and focused on patient safety above all else.  For the good of patients and to further scientific knowledge, we pursue the highest quality and most rigorous research, and we welcome the opportunity to contribute our evidence."

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