IPF

Disease

Disease Profile

IPF (idiopathic pulmonary fibrosis) is a chronic, progressive interstitial lung disease characterized by increasing fibrosis that impairs oxygen transfer. It generally affects older adults and can lead to progressive respiratory failure.

Category
interstitial lung disease
Prevalence
Estimated prevalence is 13 to 20 per 100,000 people worldwide; about 100,000 people are affected in the United States.

Related News

Related Clinical Trials

NCT ID Title Status Phase
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NOT_YET_RECRUITING PHASE1
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A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Study to Evaluate the Efficacy and Safety of HSK44459 Tablets in Patients With Idiopathic Pulmonary Fibrosis

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NCT07493031

A PhaseⅠ Study of HW252001 in Healthy Subjects

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A Phase Ia Clinical Trial of HW241045

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NCT07169253

Prognostic Score Comparison in IPF and HP

COMPLETED
NCT07139925

Assessment of Self-Care in Patients With Idiopathic Pulmonary Fibrosis (IPF)

ACTIVE_NOT_RECRUITING
NCT07031362

The Effectiveness of Pulmonary Rehabilitation on Saturation in Patients With Idiopathic Pulmonary Fibrosis

COMPLETED NA
NCT06747923

SB17170 Phase 2 Trial in IPF Patients

RECRUITING PHASE2
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Diarrheal Adverse Events in Caucasian Patients With Idiopathic Pulmonary Fibrosis Undergoing Treatment With Nintedanib

ACTIVE_NOT_RECRUITING
NCT06714188

Application of Personalized Palliative Care in Patients With Newly Diagnosed Idiopathic Pulmonary Fibrosis

COMPLETED