A rare lung disease often terminal, idiopathic pulmonary fibrosis
(IPF) is an interstitial lung disease affecting the lung
interstitium. Patients diagnosed with IPF suffer an extreme lung
deterioration resulting a decline in the lung functioning. IPF causes
'pulmonary fibrosis', which basically means damaging of the lung
tissues. Breathing distress is the most common intricacy involved
with idiopathic pulmonary fibrosis.
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The cause of idiopathic pulmonary fibrosis still remains unknown,
however, it is mostly linked with excessive inhalation of smoke or
dust, exposure to unhealthy gases and chemicals and smoking of
cigarettes. IPF may also be caused due to genetic predisposition or
develop from other lung condition.
Some of the medical conditions, which may develop in a patient with
idiopathic pulmonary fibrosis (IPF) include obstructive sleep apnea,
chronic obstructive pulmonary disease, coronary artery disease and
gastro oesophagal reflux disease. A set of guidelines has been
released for managing such conditions accordingly.
In the recent years, higher incidence of idiopathic pulmonary
fibrosis has been noticed, which has fueled the demand for idiopathic
pulmonary fibrosis therapeutics. The introduction of novel medicines
and advancement in treatment methods of the disease has further
supplemented the overall growth of the market. Nintedanib and
Pirfenidone are the two most common anti-fibrotic drugs used for the
treatment of idiopathic pulmonary fibrosis.
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There is no absolute cure for idiopathic pulmonary fibrosis available
as yet. A large portion of the treatment is directed to provide
temporary relieve to the patients. Failure to provide a complete cure
and limited treatment options are considered as major setbacks of the
market. Limited drug options with low efficiency are further
hindering the growth of the global idiopathic pulmonary fibrosis
market.
Greater focus on effective drug treatment of idiopathic pulmonary
fibrosis has led to the development of few quality drugs such as
Vargatef and Ofev. These drugs effectively reduce the patient’s
discomfort and ease the functioning of the lung. In addition,
increasing R&D programs for development of new therapies to
successfully treat IPF in expected to favor the market in the near
future. For instance, recently two major pharmaceuticals companies
Inventiva SAS and Boehringer Ingelheim GmbH have decided to jointly
work on developing potential new treatments for IPF.
On the basis of region, the global idiopathic pulmonary fibrosis
therapeutics market has been segmented into six key regions namely
North America, Latin America, Western Europe, Eastern Europe, Asia
Pacific (APAC), and the Middle East & Africa. Europe and North
America are considered as the two largest market of idiopathic
pulmonary fibrosis therapeutics. In addition, the presence of major
pharmaceutical companies in these two regions has positively impacted
the growth of the market. Countries such as the US, Canada, Germany,
France and Britain have accounted for a healthy demand of idiopathic
pulmonary fibrosis therapeutics attributed to the increasing number
of IPF incidence occurring in these countries. The global IPF
therapeutics market is expected to register a healthy growth in the
upcoming years.
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Few of Key players in the global idiopathic pulmonary fibrosis
therapeutic market include AdAlta Pty Ltd., Biogen, Inc., Angion
Biomedica Corp., Chong Kun Dang Pharmaceutical Corp., FibroGen, Inc.
Progenra, Inc, Boehringer Ingelheim GmbH and Vectura Group plc. Most
companies the focusing on further product development and offer a
wider range of IPF therapeutic treatments.
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