US biotech firm InterMune (Nasdaq: ITMN) says that Germany’s private Institute for Quality and Efficiency in Health Care (IQWiG) has issued a negative report on the benefit assessment of Esbriet (pirfenidone) for the treatment of mild to moderate idiopathic pulmonary fibrosis (IPF).
Pirfenidone is the first Orphan Drug to be reviewed by IQWiG since new health care legislation known as AMNOG (Arzneimittelmarkt-Neuordnungsgesetz) was enacted in January of 2011. Last week, AstraZeneca’s blood thinner was the first drug to gain approval under the new regimen (The Pharma Letter December 16).
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