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Your unwavering commitment to care is what leads the way forward—even when the path is still in progress

IPF and PPF are rare, difficult to diagnose, and devastating for patients and their families.1,2 Yet each day, physicians like you are traversing these challenges, taking steps to identify and manage these conditions and moving toward a future with hope for better outcomes.

As the journey of IPF and PPF continues to unfold, make a selection below to see where we are currently and where we hope to go.

Review the current landscape of IPF and PPF

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 Explore how the management of IPF and PPF is evolving

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IPF, idiopathic pulmonary fibrosis; PPF, progressive pulmonary fibrosis.

  1. Wijsenbeek M, Cottin V. Spectrum of fibrotic lung diseases. N Engl J Med. 2020;383(10):958-968.

  2. Zibrak JD, Price D. Interstitial lung disease: raising the index of suspicion in primary care. NPJ Prim Care Respir Med. 2014;24:14054.

PC-NO-102660-26.03.2026