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INTERMUNE FILES NDS FOR ACTIMMUNE IN CANADA.


InterMune (Nasdaq: ITMN), Burlingame, Calif., has filed a New Drug Submission (NDS) with the Therapeutic Products Programme of Health Canada (TPP TPP - Tangential Proper Part of (spatial reasoning)
TPP - Tape Preparation Program
TPP - Tarapoto, Peru - Tarapoto (Airport Code)
TPP - Teach Pendant Program
TPP - Teacher Professional Partnership
TPP - Technical Partner Programme
TPP - Technical Performance Plan
TPP - Technical Project Planning (US Army Corps of Engineers)
TPP - Technological Products and Processes
TPP - Technology & Policy Program (Massachusetts Institute of Technology)
) to market ACTIMMUNE(R) (Interferon gamma-1b) in Canada for chronic granulomatous granulomatous /gran·u·lom·a·tous/ (-lom´ah-tus) containing granulomas. disease (CGD CGD - Caixa Geral de Depósitos (Portuguese bank)
CGD - Canonical Gradient Descent
CGD - Center for Global Development
CGD - Chronic Granulomatous Disease
CGD - Climate and Global Dynamics (US National Center for Atmospheric Research)
CGD - Coast Guard District
CGD - Combined Graphic Display
CGD - Comptroller General Decision
CGD - Course Graduation Date
) and severe, malignant osteopetrosis oste·o·pe·trotic (-trt, both life-threatening childhood diseases. The TPP has granted Priority Review status to the NDS, and the company expects approval within six months, as there are no other effective treatments available for these diseases. ACTIMMUNE(R) is currently marketed in the United States for CGD and severe, malignant osteopetrosis.

"In the United States, physicians have more than ten years of experience using ACTIMMUNE(R) in children," said W. Scott Harkonen, M.D., CEO and president of InterMune. "In Canada there is currently no effective treatment approved for CGD or osteopetrosis, and with ACTIMMUNE's strong safety record, we look forward to ACTIMMUNE(R) being available to Canadian physicians and patients."

In 1990, the U.S. Food and Drug Administration (FDA) approved ACTIMMUNE(R) for reducing the frequency and severity of serious infections associated with CGD, a rare, inherited deficiency of the immune system that leaves patients vulnerable to frequent and severe bacterial and fungal infections. These infections often require hospitalization and can be fatal.

In February 2000, the FDA approved ACTIMMUNE(R) for delaying the time to disease progression in patients with severe, malignant osteopetrosis. Severe, malignant osteopetrosis is a life-threatening congenital disorder in which an overgrowth of bony structures leads to blindness, deafness and increased susceptibility to infection. ACTIMMUNE(R) is the only FDA-approved treatment for severe, malignant osteopetrosis or CGD.

InterMune Pharmaceuticals, Inc. is a biotechnology company dedicated to the development and commercialization of innovative products for the treatment of serious pulmonary and infectious diseases and cancer. InterMune currently markets ACTIMMUNE(R) (Interferon gamma-1b) Injection in the United States for the treatment of chronic granulomatous disease (CGD) and severe, malignant osteopetrosis.

For more information, visit InterMune's web sites at http://www.intermune.com and http://www.actimmune.com or call 415-433-5381.
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Publication:Worldwide Biotech
Date:Feb 1, 2001
Words:329
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