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Opinion|Videos|September 19, 2024

The Future of Idiopathic and Progressive Pulmonary Fibrosis Treatment

Author(s)Paul Frohna, MD, PhD

An expert physician discusses the potential role of novel agents in the management of idiopathic and progressive pulmonary fibrosis.

Episodes in this series

EP. 1 Symptoms, Manifestations and Mortality Rate of IPF

EP. 1 Symptoms, Manifestations and Mortality Rate of IPF

EP. 2 How the GAP Program Helps Determine Patient Prognosis, and Risk Factors for Developing IPF/PPF

EP. 2 How the GAP Program Helps Determine Patient Prognosis, and Risk Factors for Developing IPF/PPF

EP. 3 Epidemiology Facts, Differential Diagnosis, and Arriving at a IPF or PPF Diagnosis

EP. 3 Epidemiology Facts, Differential Diagnosis, and Arriving at a IPF or PPF Diagnosis

EP. 4 Critical Early Diagnoses and Acute Exacerbations in IPF and PPF

EP. 4 Critical Early Diagnoses and Acute Exacerbations in IPF and PPF

1 KOL is featured in this series.

EP. 5 Exploring the Role of Non-Pharmacological Modalities and Multidisciplinary Care in Patients with Idiopathic and Progressive Pulmonary Fibrosis

1 KOL is featured in this series.

EP. 6 Managing Acute Exacerbations and the Psychosocial Aspect of Idiopathic and Progressive Pulmonary Fibrosis

1 KOL is featured in this series.

EP. 7 Key Unmet Needs Associated with Idiopathic and Progressive Pulmonary Fibrosis

EP. 8 The Roles of Biomarker Testing and HRCT in IPF and PPF

EP. 8 The Roles of Biomarker Testing and HRCT in IPF and PPF

EP. 9 Unmet Needs and the Role of AI in Earlier Disease Detection

EP. 9 Unmet Needs and the Role of AI in Earlier Disease Detection

1 KOL is featured in this series.

EP. 10 Adverse Events Associated with Anti-Fibrotic Therapies

1 KOL is featured in this series.

EP. 11 Investigational Agents for Idiopathic and Progressive Pulmonary Fibrosis

1 KOL is featured in this series.

EP. 12 The Future of Idiopathic and Progressive Pulmonary Fibrosis Treatment

EP. 13 K-Cast Written Summary. Exploring Key Unmet Needs in Idiopathic Pulmonary Fibrosis

EP. 13 K-Cast Written Summary. Exploring Key Unmet Needs in Idiopathic Pulmonary Fibrosis

An investigational PDE4 inhibitor has been shown to delay progression of disease at 12 weeks in patients with IPF. Why is this exciting for pulmonologists and for patients with IPF as a whole?
How do you see these investigational therapies being implemented into future treatment paradigms for patients with IPF/PPF?

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