The Cystic Fibrosis drugs in development market research report provides comprehensive information on the therapeutics under development for Cystic Fibrosis, complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses key aspects of the companies and drugs in development for Cystic Fibrosis. Buy the report here.
The report also covers the descriptive pharmacological action of the therapeutics and the latest news and press releases. Additionally, the report provides an overview of the key players involved in therapeutic development for Cystic Fibrosis and features dormant and discontinued products.
GlobalData tracks 151 drugs in development for Cystic Fibrosis by 114 companies/universities/institutes. The top development phase for Cystic Fibrosis is preclinical with 63 drugs in that stage. The Cystic Fibrosis pipeline has 139 drugs in development by companies and 12 by universities/ institutes. Some of the companies in the Cystic Fibrosis pipeline products market are: Sionna Therapeutics, Vertex Pharmaceuticals and Recode Therapeutics.
The key targets in the Cystic Fibrosis pipeline products market include Cystic Fibrosis Transmembrane Conductance Regulator, Anoctamin 1, and Epithelial Sodium Channel.
The key mechanisms of action in the Cystic Fibrosis pipeline product include Cystic Fibrosis Transmembrane Conductance Regulator Activator with 53 drugs in Pre-Registration. The Cystic Fibrosis pipeline products include nine routes of administration with the top ROA being Inhalational and 14 key molecule types in the Cystic Fibrosis pipeline products market including Small Molecule, and Gene Therapy.
Cystic Fibrosis overview
Cystic fibrosis (CF) is an inherited disease that causes mucus to build up and clog some of the body’s organs, particularly the lungs and pancreas. Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. Symptoms include wheezing, breathlessness, repeated lung infections, inflamed nasal passages or a stuffy nose, and severe constipation. Risk factors include family history and race (Northern European ancestry). Treatment includes antibiotics, mucus-thinning medications, bronchodilators, and oral pancreatic enzymes.
For a complete picture of Cystic Fibrosis’s pipeline drug market, buy the report here.
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