The study analyzed that the IPF pipeline comprised of 97 therapeutic candidates, of which 15 are in Phase II stage of development. The lack of complete cure for IPF fuels the extensive research and development for the IPF therapeutic. Various drugs are being developed as novel and promising therapeutics for the treatment of IPF.
Browse the Report Summary at: https://www.psmarketresearch.com/market-analysis/idiopathic-pulmonary-fibrosis-therapeutics-market
Browse
Report Sample at: https://www.psmarketresearch.com/market-analysis/idiopathic-pulmonary-fibrosis-therapeutics-market/report-sample
U.S.
Food and Drug Administration (FDA) and European Medicines Agency (EMA) granted
ODD to more than 10 drugs. As per the FDA, its Office of Orphan Products
Development (OOPD) mission is to advance the evaluation and development of
products (drugs, biologics, devices, or medical foods) that demonstrate promise
for the diagnosis and/or treatment of rare diseases or conditions. Tipelukast,
also known as MN-001, is under Phase II stage of development by MediciNova,
Inc. for the treatment of IPF. The drug was granted ODD for the treatment of
IPF, which will provide MediciNova with seven years of marketing exclusivity if
it is approved for IPF. Some of the key players developing drugs candidates for
the treatment of IPF are Bristol-Myers Squibb Company, F. Hoffmann-La Roche
Ltd., Merck & Co., Inc., Global Blood Therapeutics, Inc., Asahi Kasei
Corporation, Beijing Tide Pharmaceutical Co., Limited, FibroGen, Inc., Chong
Kun Dang Pharmaceutical Corp., Galapagos NV, Kadmon Holdings, Inc., MediciNova,
Inc., and Promedior, Inc.
No comments:
Post a Comment