Interstitial Lung Fibrosis is an indication for drug development with over 340 pipeline drugs currently active. According to GlobalData, preregistered drugs for Interstitial Lung Fibrosis have a 100% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Interstitial Lung Fibrosis compared to historical benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Interstitial Lung Fibrosis overview
Interstitial Lung Fibrosis or interstitial lung disease (ILD) is a group of diseases that cause scarring of the lungs (fibrosis) or lung parenchyma. If untreated it can lead to respiratory failure and death. Symptoms start with inflammation and can result in bronchiolitis, vasculitis, and alveolitis. Exposure to hazardous chemicals or materials like asbestos, hypersensitivity, drug-induced, underlying autoimmune conditions, family history, smoking, and exposure to radiation are common factors while SOB, discomfort in the chest, loss of appetite, dry cough are common symptoms. Validated by chest x-ray, biopsy, bronchoscopy, PFT. Corticosteroids are prescribed to treat inflammation, oxygen therapy if breathlessness and other symptomatic management.
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For a complete picture of PTSR and LoA scores for drugs in Interstitial Lung Fibrosis, buy the report here.
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