PatientsHealthcare PractitionersInvestigators


North American Trial Sites

European Trial Sites

What is IPF?

Additional Resources


Additional Resources

Helpful Links for Patients

Websites with information for IPF patients:

  • FIGHT IPF - A support site for IPF patients, their family, and caregivers.
    www.fightipf.com

  • Coalition for Pulmonary Fibrosis - A nonprofit organization founded to further education, patient support, and research efforts for pulmonary fibrosis (pf), specifically IPF. This website includes information for patients and a list of support groups.
    www.coalitionforpf.org

  • American Lung Association - The American Lung Association® is the oldest voluntary health organization in the United States and offers programs and strategies for fighting lung disease.
    www.lungusa.org

  • Canadian Lung Association - The Canadian Lung Association is a non-profit and volunteer-based health charity which has a mission of leading nationwide and international lung health initiatives, preventing lung disease, helping people manage lung disease and promoting lung health.
    www.lung.ca

Additional Resources:

If you need further information regarding these trials please call the InterMune Medical Information Department at 1-888-486-6411 (1-888-ITMN-411).

InterMune, Inc. The future of IPF

The information on this website concerns an investigational medication that has not been approved by the Food and Drug Administration.

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