Texas
Insider Report: WASHINGTON D.C. Today Representative
Bill Flores (R-TX) and Senator Thom Tillis (R-NC) re-introduced
the Hatch-Waxman Integrity Act in the House of Representatives
and Senate. The legislation would help ensure that alternative procedures for
challenging drug patents do not tilt the playing field contrary to Hatch-Waxmans design.This
bill will restore balance and integrity to the patent system and
ensure drug manufacturers have the proper incentives
to continue developing life-saving medications.
Innovative pharmaceutical companies continue to develop new and exciting
therapies to help change the lives of patients around the world" said
Representative Flores. The Hatch-Waxman Integrity Act supports continued
innovation by restoring an effective balance between the interests of brand-name
and generic drug manufacturers. By ensuring a balanced process to challenge
pharmaceutical patents we make certain that American patients will continue to
benefit from research new discovery and medical innovation."
The biotechnology and life sciences industry undertakes tremendous risk and
costs to develop new life-saving drugs with the vast majority of
products never making it to the market at great expense to the
manufacturer. These drugs save millions of lives every year and are a
critical component of our nations healthcare system. While it is
important to call out bad actors who price gouge we must allow sufficient time
and balance so companies can continue to develop life-saving drugs and help
people with the countless illnesses and diseases that affect millions of
Americans" said Senator Tillis. The Hatch-Waxman Integrity
Act will restore a proper balance in the market so
that companies will continue to spend billions of dollars to
develop life-saving and life-altering treatments. I want to thank
Senator Hatch for his leadership on this issue and I look forward to building
support for this bill within the Senate."
Background:
The Hatch-Waxman Integrity Act of 2019 would require a generic
manufacturer wishing to challenge a brand-name drug patent to choose between
the Hatch-Waxman framework which affords certain advantages
such as being able to rely on the drug innovators safety and efficacy studies
for FDA approval and inter partes review or IPR which is cheaper
and faster than Hatch-Waxman litigation but does not provide
the advantages of a streamlined generic approval process. The bill would apply
similarly to patents on biologics.
The bill would preserve Hatch-Waxman as the standard path for
generic manufacturers to challenge brand patents while keeping IPR as an
option where other interests come into play. It would not have any impact on
the use of IPR by the tech community.
A copy of the bill text is available HERE.