Abstract:
:A new regulatory pathway established last year allows drugs with dramatic early clinical promise to be expedited to the market quicker than ever before. To date, most of these 'breakthrough' designations have gone to cancer agents, raising the prospect of faster access to the latest lifesaving therapies for the estimated 4,500 people newly diagnosed with cancer each day in the US. Elie Dolgin looks at what sets these breakthrough medicines apart.
journal_name
Nat Medjournal_title
Nature medicineauthors
Dolgin Edoi
10.1038/nm.3245subject
Has Abstractpub_date
2013-06-01 00:00:00pages
660-3issue
6eissn
1078-8956issn
1546-170Xpii
nm.3245journal_volume
19pub_type
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