x*1
2 楼
In some articles they mentioned March 9.
E*X
3 楼
I remembered two events: one on May 4th and one on May 9th.
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4 楼
The MAA is the second major regulatory filing by InterMune to seek approval
to market pirfenidone for the treatment of patients with IPF. The New Drug
Application (NDA) for pirfenidone was filed by InterMune in the United
States in early November 2009. The U.S. Food and Drug Administration's (FDA)
Pulmonary-Allergy Drugs Advisory Committee (PADAC) is scheduled to discuss
the company's NDA for pirfenidone on March 9, 2010. Based on the
Prescription Drug User Fee Act (PDUFA), the FDA has set an ac
to market pirfenidone for the treatment of patients with IPF. The New Drug
Application (NDA) for pirfenidone was filed by InterMune in the United
States in early November 2009. The U.S. Food and Drug Administration's (FDA)
Pulmonary-Allergy Drugs Advisory Committee (PADAC) is scheduled to discuss
the company's NDA for pirfenidone on March 9, 2010. Based on the
Prescription Drug User Fee Act (PDUFA), the FDA has set an ac
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