Cystic Fibrosis - Drug Pipeline Landscape, 2022 - Overview, Trends, Growth, Demand, Key Players Analysis and Forecast to 2031

New York, Global Cystic Fibrosis - Drug Pipeline Landscape, 2022 report from Global Insight Services is the single authoritative source of intelligence on Cystic Fibrosis - Drug Pipeline Landscape, 2022. The report will provide you with analysis of impact of latest market disruptions such as Russia-Ukraine war and Covid-19 on the market. Report provides qualitative analysis of the market using various frameworks such as Porters' and PESTLE analysis. Report includes in-depth segmentation and market size data by categories, product types, applications, and geographies. Report also includes comprehensive analysis of key issues, trends and drivers, restraints and challenges, competitive landscape, as well as recent events such as M&A activities in the market.

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Cystic Fibrosis (CF) is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. In people with CF, a defective gene causes a thick, sticky buildup of mucus in the lungs, pancreas, and other organs. In the lungs, the mucus clogs the airways and traps bacteria leading to infections, extensive lung damage, and eventually, respiratory failure. In the pancreas, the mucus prevents the release of digestive enzymes that the body needs to break down food and absorb vital nutrients.

In cystic fibrosis, a defect (mutation) in CFTR gene, changes a protein that regulates the movement of salt in and out of cells. Many different defects can occur in the gene. The type of gene mutation is associated with the severity of the condition.

Symptoms of Cystic Fibrosis include trouble with bowel movements or frequent, greasy stools, wheezing or trouble breathing, frequent lung infections, Infertility.

Healthcare providers diagnose cystic fibrosis with by using different tests including newborn screening, sweat test, genetic tests, chest X-rays, sinus X-rays, lung function tests and sputum culture.

Treatment of cystic fibrosis include medications, medications targeting genes, vest therapy, pulmonary rehabilitation, and surgical procedures.

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Methodology
The research process includes extensive secondary research on public domain and other authentic sources to add or update the pipeline products information. The secondary research sources include, but are not limited to company websites, annual reports, financial reports, company pipeline chart, investor presentations and SEC filings, journals and conferences, and clinical trials registries.

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Scope
The pipeline landscape report provides analysis of pipeline products based on several stages of development ranging from Discovery to Pre-Registration. The report provides a review of pipeline therapeutics by companies based on information derived from company and industry-specific sources. The pipeline report covers assessment of therapeutics by mechanism of action (MoA), drug target, route of administration (RoA) and molecule type. Comprehensive profiles of the pipeline products with details such as company overview, development stage; molecule type, target, mechanism of action, route of administration, dosage form, regulatory designations, key deals, clincial trials, and key upcoming milestones are included.

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