Patents &
Exclusivity of Drug Products in US Market
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Patents
and exclusivity work in a similar fashion but are distinctly different from
one another.
Patents
are granted by the patent and trademark office anywhere along the development
lifeline of a drug and can encompass a wide range of claims.
Exclusivity
refers to certain delays and prohibitions on approval of competitor drugs
available under the statute that attach upon approval of a drug or of certain
supplements. In other words exclusivity is exclusive marketing rights granted by
the FDA upon approval of a drug and can run concurrently with a patent or
not. Exclusivity is a statutory provision and is granted to new drug
application (NDA) or abbreviated new drug application holder if statutory
requirements are met. Exclusivity was designed to promote a balance between
new drug innovation and generic drug competition.
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Patent terms are set
by statute. Currently, the term of a new patent is 20 years from the
date on which the application for the patent was filed in the United
States. Many other factors can affect the duration of a patent.
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Patents and exclusivity
apply to drugs in different ways. Patents can be issued or expire at
any time regardless of the drug’s approval status. Exclusivity attaches
upon approval of a drug product if the statutory requirements are met. Some
drugs have both patent and exclusivity protection while others has just one
or neither. Patents and exclusivity may or may not run concurrently and
may or may not cover the same aspects of the drug product.
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Type
of Exclusivity
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Tenure
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Orphan Drug Exclusivity (ODE)
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7 years
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New Chemical Entity Exclusivity (NCE)
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5 years
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Generating Antibiotic Incentives Now (GAIN)
Exclusivity
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5 years added to certain exclusivities
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New Clinical Investigation Exclusivity
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3 years
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Pediatric Exclusivity (PED)
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6 months added to existing
Patents/Exclusivity
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Patent Challenge (PC)
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180 days (this exclusivity is for ANDAs only)
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Competitive Generic Therapy (CGT)
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180 days (this exclusivity is for ANDAs only)
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