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TWN Info Service on Intellectual
Property Issues (Nov07/01)
1 November 2007
RUSH IS ON FOR PATENTS ON AVIAN FLU VIRUSES AND VACCINES
A recent research paper (July 2007) titled "Some Intellectual Property
Issues Related to H5N1 Influenza Viruses, Research and Vaccines"
by Edward Hammond from the US-based The Sunshine Project has revealed
a recent spike in the number of patent applications covering the influenza
virus (or parts of it), as well as vaccines, treatments and diagnostics.
The paper is available at http://www.twnside.org.sg/avian.flu_papers.htm
The paper reveals recent statistics about patent applications related
to avian influenza and gives an insight into the patent claims that
are made by the applicants, its impact on access and on R&D and
the country of origin of the patent applicants. According to Hammond, further claims on recent isolates exist
but are not yet available due to delays in submission of applications
and publication of patent claims.
Below is a report on the research paper. It was published in the South-North
Development Monitor (SUNS) on 30 October. It is reproduced here with
the permission of the SUNS. Any reproduction or re-circulation requires
the permission of the SUNS (sunstwn@bluewin.ch).
With best wishes
Martin Khor
TWN
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RUSH IS ON FOR PATENTS ON AVIAN FLU VIRUSES AND VACCINES
Geneva, 29 Oct 2007: By Sangeeta Shashikant (TWN)
Even as health authorities increasingly worry about the possible occurrence
of a deadly avian influenza pandemic, there has been a dramatic rise
in international patent applications related to the influenza virus,
and vaccines and treatments related to it.
This trend is of grave concern to public health officials and civil
society groups in developing countries who fear that patents relating
to avian flu will threaten the access of the poor and of people in developing
countries to affordable vaccines and treatment.
Many of these countries have been freely sharing avian influenza viruses
under the WHO's Global Influenza Surveillance Network, in the hope that
they will be able to obtain timely, affordable and sufficient access
to vaccines and other benefits to battle a pandemic should it occur.
However, if the viruses (or parts thereof) or vaccines and technologies
and methods to make them are patented, the prices of the vaccines may
become higher and other producers may also be hindered from making the
vaccines.
A recent research paper (July 2007) titled "Some Intellectual Property
Issues Related to H5N1 Influenza Viruses, Research and Vaccines"
by Edward Hammond from the US-based The Sunshine Project has revealed
a recent spike in the number of patent applications covering the influenza
virus (or parts of it), as well as vaccines, treatments and diagnostics.
Until 1993, there had been little or no such patent activity. The paper
shows that in 2006 however, more than 30 international patent applications
were filed under the Patent Cooperation Treaty (PCT) on influenza vaccines
alone, making it the year with the highest number of applications on
such vaccines.
World Intellectual Property Organization (WIPO) data indicate that during
the first half of 2007, as many influenza vaccine patent claims have
been filed as in the whole of 2006, meaning that this year is on track
to at least double the record set in 2006.
More than 80% of these applications originate from developed countries,
with at least 50% of these applications originating from the US.
The paper also identified 39 PCT patent applications between 2001 and
2007 for medicines, vaccines, microbes, peptides, nucleic acids and
immunoassays with the term "H5N1" in the claims. They include
patent applications on diagnostics, detection technologies, sequences,
etc.
H5NI is a subtype of the Influenza A virus that can cause illness and
death in humans and animals, and there are fears that the virus could
mutate to be spread through human-to-human transmission, and lead on
to an influenza pandemic.
The paper found that 87% of these applications had been filed in the
last 18 months (i. e. 14 in 2006 and 20 in the first half of 2007 alone).
Patent applicants from the US account for 46% of the applications.
The study reviewed recently published US and international patent data
and identified patent applications that cover H5N1 genes, gene sequences
(smaller pieces of genes), variations of those genes and their use.
The recent rate of growth of flu vaccine patent applications that make
claims specifically on H5N1-type influenza has surpassed that of influenza
vaccine claims in general.
Hammond stated that "because of the moving target' nature of influenza,
it may be assumed that further claims on recent isolates exist but are
not yet available due to delays in submission of applications and publication
of patent claims".
The author adds that what is most important are the worrying trends
and kinds of claims being lodged. These indicate a near-term (and long-term)
future in which H5N1 strains and all manner of technologies related
to using them in vaccines will be patented.
The WHO has declared a phase 3 pandemic alert (i. e. with no or limited
human-to-human transmission) and has cautioned that the world is now
closer to another influenza pandemic than at any time since 1968.
Thus, the recent increased enthusiasm in patenting comes as no surprise,
as the private sector and other institutions would see this situation
as a profit opportunity.
According to Hammond, "Some increase in patents is arguably to
be expected given rising concern about H5N1 and renewed interest in
vaccines from major pharmaceutical companies, not only for influenza,
but for "biodefence" and (often only from the North's view)
emerging infectious diseases".
"The ultimate value of the currently claimed sequences and technologies
is uncertain, but if any prove critical to combat a pandemic, it may
be enormous", Hammond
states in the paper.
This has major implications for who can manufacture the vaccines and
other related treatment products, whether there will be sufficient supplies
of vaccines in the event of a pandemic, and who can afford the medical
products.
In a number of patent applications, companies and other institutions
have made proprietary claims over viruses and their parts that originate
from developing countries. These include viruses contributed by countries
such as Indonesia, Vietnam,
China and Thailand, to the
WHO-designated collaborating centres and reference laboratories in the
Global Influenza Surveillance Network.
These laboratories are national institutions in the US, UK, Australia
and Japan that conduct tests to identify the virus strains that become
WHO-recommended vaccine seed strains, from which vaccines and diagnostics
can be developed. These strains have so far been made available to vaccine
developers and other institutions.
The fact that different players in the system have been seeking patents
over materials shared in good faith for public health reasons is a matter
of serious concern.
Patents grant an exclusive right that means that a patent holder can
deny others access to its patented subject matter including gene sequences,
research tools, diagnostic kits, vaccines or other products. Concerns
about patenting have frequently been raised amongst the international
community as it could drastically hamper research and development as
well as access to essential medical products.
An example of such a patent application is that made by St. Jude's Children's
Hospital from the US,
a laboratory designated by WHO to do certain tests.
Its patent application on "Modified Influenza Virus for Monitoring
and Improving Vaccine Efficiency", published on 8 February 2007,
claims small changes to influenza HA genes. These changes are intended
to strengthen the immune system reaction to the genetically engineered
virus. This might improve possible pandemic influenza vaccines because
people vaccinated may exhibit a stronger immune reaction against H5N1.
This patent application claims any influenza HA gene modified in a certain
way. It specifically claims the modified HA gene from an influenza virus
isolated in Vietnam
in 2004. This is the same strain whose entire HA and NA sequences have
been claimed by MedImmune (now AstraZeneca).
The study cited a number of other recent examples of patent claims over
genetic material originating from developing countries.
MedImmune (now AstraZeneca) and the US Government have filed a complicated
set of national and PCT applications over "Influenza hemagglutinin
and neuraminidase variants" that covers sequences from at least
29 influenza strains, in many cases the entire HA and/or NA genes. The
patents cover producing influenza vaccines from them by placing the
genes, or variants, onto a "backbone" of a lab-adapted influenza
strain.
Three applications are relevant to the pandemic discussion. These are:
(1) application WO2005116260 that claims the entire HA and NA sequences
from viruses originating in Hong Kong and Vietnam; (2) application WO2005116258
that claims a series of 20 H5N1 and H9N2 HA and NA sequences from viruses
originating in Vietnam and China; and (3) application WO2006098901,
the newest member of the patent family to be published that claims 48
entire HA and NA genes from 24 different Influenza A and B viruses.
In this set of applications, the US government may have rights. If
the US
government has rights, its rights would include the ability to “march
in” on the patent i.e. The government may force the company to issue
it a royalty free, irrevocable licence in the event of a national emergency.
Some US and international patent applications
list government inventors who are employees of the US Department of
Health and Human Services (HHS). The US Centres for Disease Control
(CDC), a WHO Collaborating Centre, is part of HHS.
Novavax, Inc. (US) has filed a US and PCT patent
application over "Functional influenza virus-like particles"
(VLPs). Novavax's technique is to place influenza HA, NA, and M1 genes
into another virus and to grow the hybrid virus in an insect cell culture.
This produces partial influenza viruses ("virus-like particles"
- or VLPs).
These may be useful for vaccines because they can, like a whole virus,
produce an immune reaction. In some cases, the influenza genes are changed
("optimized") for use in the insect cell system.
This patent application claims any influenza VLPs produced by its cell
culture methods as well as specific VLPs. VLPs claimed include those
made with HA and NA genes of virus strains from Indonesia and China,
as well as VLPs made from sequences 90% or more homologous (close in
genetic structure) to those particular sequences.
Another US
company, Hawaii Biotech Inc., has US and PCT applications on "Influenza
recombinant subunit vaccine".
This patent application, published on 22 February 2007, claims 12 variations
on production of a new type of influenza vaccine made in insect cells
and H5N1 vaccines made with the technology.
It specifically claims H5N1 genetic sequences from a virus isolated
in Indonesia in 2005 and another isolated in China in 1997.
It also claims sequences from an H3N2 virus isolated in China in 2002.
Yet another US
company, Protelix Inc., filed a PCT patent application (published on
3 May 2007) on "Influenza Combinatorial Antigen Vaccine".
This covers nucleotide sequences from influenza HA and NA genes, a method
for selecting them, and their use in influenza vaccines.
An advantage that Protelix claims is that it can tailor vaccine composition
to the virus strains from a specific geographic area. Protelix specifically
claims HA and NA sequences derived from recent H5N1 isolates from Thailand
and Indonesia,
as well as slight variations on those sequences, for use in vaccines.
According to Hammond,
such patent claims for dozens of HA and NA gene sequences used in current
vaccines are one way that a microbial resource can be locked up. Another
way is a "thicket" of smaller patent claims that gradually
leads to an overlapping and confusing mess of claims. Currently, both
types of problems are emerging for H5N1 viruses and vaccines.
In his paper, Hammond
also explains the "homology fishing" strategy used by patent
applicants to extend their patent controls. He states that much of the
value of an influenza virus, from a patent perspective, lies in its
particular HA and NA gene sequences.
However, as virus sequences change faster than patent applications can
be processed, patent applications are trying to reach forward in time,
and claims are written in a way that, expressed in plain language, are
the equivalent of "we claim this gene and anything like it"
(i. e. mutations that have not occurred).
While not entirely new, homology fishing, according to Hammond, may be reaching a new level of importance
with influenza-related patents because of the potentially devastating
effects of a pandemic.
The race to file patents amidst a public health disaster is not new.
It is reported that following the outbreak of Severe Acute Respiratory
Syndrome (SARS'), a form of atypical pneumonia caused by a new strain
of coronavirus in 2002, WHO coordinated a team of international scientists
and researchers.
These scientists in Canada,
Hong Kong and the US
were able to sequence the SARS virus with remarkable speed but several
of the public research institutions filed patent applications in respect
of the complete genetic sequence of the coronavirus.
According to a WHO notification of May 2003, the detailed claims in
these applications have not yet been made public but are reported to
be sufficiently broad to allow their holders to claim rights in most
diagnostic tests, drugs, or vaccines that have been or would be developed
to cope with the outbreak.
Some of the university or governmental patent applicants have themselves
begun negotiations with commercial partners to develop diagnostic tests
and other products. During this time, fears were expressed that prospective
patent holders might prevent or limit access to diagnostics, vaccines
and pharmaceutical drugs which are being developed by commercial companies
to address the SARS virus.
While SARS may no longer be a problem, similar questions have now arisen
for influenza.
(Note: The paper is available at http://www.twnside.org.sg/avian.flu_papers.htm)
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