2001 Nature Publishing Group http://biotech.nature.com
Monopoly moneyStrategies used by the pharmaceutical industry to alleviate the pain of patent expiration provide somevaluable lessons for the biotechnology sector. . .and also some cautionary tales, says Alan Dove. h.nature
There is an old saying that the inventor an exclusive market for the inven-
tion for at least 20 years from the date the
application was filed. On paper at least, all
140 nations that are currently members of
the WTO provide this level of patent pro-
patents. Twenty-five years ago, the biotech-
In most industries, including agricultur-
oup http://biotec
al and industrial biotechnology, a patent
isms and recombinant proteins. Today, it is
lishing Gr
a rapidly maturing industry, with market-
clout. But as it becomes more mature, the
industry will also begin to suffer from new
Octogenarians at the gate
On 25 April 2001, a coalition of consumer
covering some of its early products being
groups, spearheaded by a senior citizens’
just one. In this respect, pharmaceutical
2001 Nature Pub
filed a class-action lawsuit against Bristol-
sophisticated ways to protect their patents
and profits, and some of these approaches
will be broadly applicable to the biotech-
practices. Specifically, the Panthers argue
patent-listing procedures to block pending
The point of patents
competition once the patent expired. Matt
Patents were originally conceived in the 18th
century as a legal tool to encourage indus-
trial innovation. To receive a patent, an
$100 million. Bristol-Myers Squibb denies
invention must fulfill three criteria: it must
be novel, useful, and not be obvious from
has, once it gets on the market, only about
suit filed in April, plaintiffs claim that
8.5 years of effective life left before its
patent runs out. With the partial restora-
$90 million to Upsher-Smith (Minneapolis,
insecticide), methods of production (e.g., a
MN) and ESI Lederle (Philadelphia, PA), a
way of making the insecticide), or devices
(e.g., a sprayer to apply insecticides to
A Waxman–Hatch style “patent restora-
tion term” for pharmaceuticals is not avail-
able in the European Union and Canada.
marketplace, during which competitors are
prevented from selling their own versions
Waxman–Hatch style ruling would have less
Biotechnol, 19, 497, 2001). These lawsuits
impact on product sales for medicines than
it does in the United States because of the
tight price controls on prescription drugs in
extend marketing exclusivity on profitable
implemented differently in different coun-
these regions. Canada is currently in the
tries. To establish uniformity, the General
process of reviewing its patent laws in an
Agreement on Tariffs and Trade—replaced
biotechnology, and one of the issues being
1995—drew up international standards for
Alan Dove is a freelance writer working inPhiladelphia, PA ([email protected]).
(TRIPs) agreement, a patent must grant the
• VOLUME 19 • nature biotechnology 2001 Nature Publishing Group http://biotech.nature.com
However, a specific technique, such as a sur-
explains: “We are considerably behind both
delivery systems. Companies can, for exam-
gical procedure or, possibly, the delivery of a
ple, create a version of a brand-name drug
particular gene to a particular tissue, cannot
that can be given just once a day, because the
patent on the new system will enjoy an addi-
plants and animals are patentable.” The
tional 20 years of market exclusivity. For
example, CBAC’s Gold says: “The gene ther-
CBAC is soliciting public input on its draft
example, Pfizer (New York) recently intro-
apy or the vector can be patented, but the
report, expecting to submit its final recom-
duced Glucotrol XL, a once-daily version of
injection into the body is not patentable.
mendations to Parliament in late June.
its popular diabetes drug, Glucotrol (glip-
Usually it won’t make a big difference, but
izide). The new product constitutes a novel
Patent proof
formulation of the original branded drug,
Even with the implementation of a patent-
Industry experts agree that some biotech-
h.nature
restoration term, all drug patents eventually
rays—are still too new to predict the impact
become aggressive in their attempts to avoid
of the expiration of their patents. If the
the inevitable loss of profit. According toanalysts, the absence of prescription-drugprice controls, the presence of a robust
Developing new delivery techniques to extend marketing
generic-drug industry, and easy access to
oup http://biotec exclusivity—so-called evergreening—may eventually become
civil courts, have combined to make theUnited States the focus of most efforts to
more difficult for biotechnology companies in Europe and Canada, neither of which allows patents on “medical treatments and
Michael Krensavage, a health care analyst
lishing Gr surgical methods.”
York), says that pharmaceutical companies“have been very creative” about protectingexclusivity for their blockbuster drugs. Forexample, in 1993, SmithKline Beecham
Partners (New York), says: “There’s very lit-
tle risk [of carrying out such trials], because
the pharmaceutical industry, chip manufac-
all the toxicology is well known to the FDA.”
turers might try to block generic competi-
2001 Nature Pub
generic version of its ulcer drug Tagamet
Generic versions of the original drug may be
tion in similar ways. Alternatively, the DNA
(cimetidine) infringed its patent because the
manufactured and sold, but the new brand-
chip business might follow the pattern of
pills were the same color. “The way the law
ed formulation has the distinct competitive
rapid pace of innovation has often rendered
FDA-required halt period) to settle these
things in court,” says Krensavage. The gener-
ic drug cannot be sold while the case is in
tions, drug makers can try to deliver the
The trouble with proteins
drug in more innovative ways, such as trans-
monopoly is therefore extended. Krensavage
dermal patches or implanted capsules.
protein therapeutics are highly resistant to
explains: “Millions of dollars a day in sales
generic competition, primarily because of
adds up to a lot of attorneys’ fees, so while
needle-free ways to deliver drugs through
the regulatory structure of drug-approval
your efforts don’t have to be valid, you can
the skin (e.g., PowderJect; Oxford, UK) or
agencies, such as the US FDA. A therapeu-
lungs (e.g., Inhale; San Carlos, CA).
tic small molecule is classified as a “drug”,
Lawsuits do not even have to go to court in
Pharmaceutical companies are keen to col-
but proteins (and vaccines) are considered
order to extend a brand-name monopoly. In a
laborate with such companies. Indeed, one
“biologics” and are governed by different
motivation for Johnson & Johnson’s (New
increasingly prevalent, a brand-name manu-
Brunswick, NJ) recent high-profile $10 bil-
facturer will sue the generic company, and the
lion acquisition of drug-delivery pioneer
generic small molecule after the patent has
two companies then reach a “settlement” in
expired needs only to demonstrate that it is
delivery systems that it intends to use to
chemically and biologically equivalent to
competitor to stay out of the market. Drug
rejuvenate its ageing drugs pipeline (Nat.
the brand-name product—tests that are far
manufacturers deny accusations that these
Biotechnol. 19, 398, 2001).
less expensive to conduct than full-scale
arrangements violate antitrust laws—and
clinical trials de novo. However, a biologic
between patent protection and the spirit of
to carry out a completely new set of clinical
more difficult for biotechnology companies
trials to bring the generic product to mar-
groups alike say that such “settlements” smack
ket, making generic proteins a less favor-
of collusion (see “Octogenerians at the gate”).
allows patents on “medical treatments and
able business proposition (Nat. Biotechnol.
surgical methods.” The prohibition is subtle:
19, 117, 2001). New delivery routes
a drug can be patented under “unique com-
A more sustainable approach for small-mol-
position of matter,” and a device that deliv-
tics are avidly pursuing patentable improve-
ecule drug developers is to formulate brand-
ers the drug can be patented as a “device”. 2001 Nature Publishing Group http://biotech.nature.com
(Indianapolis, IN), for example, was able to
Agricultural agro
numbers: most of the patents in the field are
The situation for agricultural biotechnology
is less clear, in that the most successful prod-
companies, making it unlikely that a generic
ucts to date—Bt transgenic crop strains and
manufacturer could compete successfully.
herbicide-tolerant plants—still have more
Still, as future patent rules evolve, biotech-
begun phase 3 clinical trials of Aranesp, a
than 10 years of patent protection remain-
nology companies, like their pharmaceutical
version of recombinant human erythropoi-etin that will last longer in the bloodstream. Amgen’s original erythropoietin patent
The most successful products to date—Bt transgenic crop strains and herbicide-tolerant plants—still have more than 10 years of
wise not to rest on their laurels. Pedro de
patent protection remaining. h.nature
Noronha Pissarra, president of Biotecnol(Porto Salvo, Portugal), explains: “Oneshould not forget that biotechnologygenerics are already being marketed out-
counterparts, will have to continue to swal-
low the bitter pill of patent expiration.
States, and to my knowledge they are well
company intends to pursue the only surefire
accepted.” Pissarra suggests that Asia and
strategy for protecting its lead: “It is very
oup http://biotec
South America could be ideal locations for
difficult to tell in agricultural biotechnology
bioinformatics are also expected to acceler-
marketing biogenerics, because full-scale
be.more than ten years’ time. It’s our inten-
possibly driving older products into obsoles-
tion to develop that technology that will be
cence before their patents have expired. lishing Gr
state of the art, rather than to focus on
“Quite aside from any generic competition. .
.this is a time of scientific ferment, so you’ve
got intense competition among innovators,”
companies also enjoy strength in a lack of
2001 Nature Pub
P I A D E H N E __________________________________________________ Born in Düsseldorf , Germany, Pia Dehne received her Master of Fine Arts from and studied 1988 -1994 under Professor Markus Lüpertz at the Kunstakademie Düsseldorf in Germany. Dehne later lived in Berlin, and after her second solo exhibition at Gallery Achim Kubinski there in 1999 she moved to New York. She currently lives
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