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Nascent Alzheimer's disease biomarker market provides opportunities for pharma companies
Research report: PharmaFocus: Biomarkers in Alzheimer’s Disease
From a commercial standpoint, the Alzheimer's disease (AD) biomarkers market is still relatively young. Biomarkers for Alzheimer's disease can be classified in terms of pathological mechanism and also in terms of the assay technology used to detect and assess the biomarker.
Magnetic resonance imaging (MRI) and fluorodeoxyglucose-positron emission tomography (FDG-PET) are valuable biomarker tools for assessing brain structure and function. However, these imaging tests can be administered in Alzheimer's disease patients, at least at the basic level, without the need for AD-specific products or modifications.
These tools don’t provide as many opportunities for further development in AD compared with other biomarkers and thus there aren’t many companies that have been involved in the development and commercialization of structural and functional imaging biomarker products for AD.
Molecular biomarkers of AD, on the other hand, present more viable opportunities for the development of novel assays with commercial potential. At the time of this writing, Amyvid ([18F] Florbetapir), an amyloid positron emission tomography (PET) imaging ligand marketed by Eli Lilly, is the only diagnostic assay approved by the Food and Drug Administration (FDA) for AD.
Despite Lilly’s market monopoly at present, there are several similar amyloid PET imaging ligands in the pipeline, with GE Healthcare’s [18F] Flutemetamol and Piramal’s [18F] Florbetaben currently undergoing regulatory review in the US and the European Union (EU), and these are likely to provide active competition.
There are also several companies actively developing fluid-based biomarker panel assays for AD, including Innogenetics, which has produced assay kits for amyloid and tau proteins that are widely used in academic research and in clinical drug development. Some of these Innogenetics AD biomarker kits have received CE (Conformité Européenne) marking in the EU, but to date, none are FDA approved for clinical diagnostic use in the US.
Blood-based assays for Alzheimer's disease biomarkers hold great promise as screening tests that can be widely applied in a cost-effective manner and are a major unmet need for AD. Several companies, such as Exonhit, Ctyox, Proteome Biosciences, DiaGenic, and Amarantus, have products in development that, if validated, may satisfy this need.
Novel biomarker products would be welcomed to meet the numerous unmet needs in the AD biomarker market
The AD biomarker field is rife with unmet needs, both environmental and clinical. Environmental unmet needs include limited physician knowledge of the appropriate application of existing biomarker tools, as well as limited public awareness of the disease, which prevents people from seeking a clinical diagnosis. Often, Alzheimer’s symptoms are ascribed to normal aging. Cost and accessibility are currently limiting the widespread use of the available biomarker tools, since most of these are imaging-based technologies (MRI, PET) that can be quite expensive and require access to specialized imaging facilities.
There are also several unmet needs intrinsic to the biomarkers themselves. There is a lack of biomarkers that adequately assess the multiple pathological processes that are thought to contribute to AD; although tools to assess amyloid as a biomarker for AD have been actively developed, molecular measures of neurodegeneration, inflammation, and oxidative stress remain limited. Consequently, there remains plenty of room in the market for products that can satisfy these needs, provided that their accuracy and validity can be demonstrated. However, there have been challenges in producing widely reproducible assays, as described below.
Existing AD biomarker assays face challenges in validation and standardization that may be addressed through public-private collaborations
The biomarker assays that have been developed suffer from a lack of standardization and validation, which has limited their clinical utility. However, the challenge of financing the large studies needed for assay validation has limited smaller companies from advancing their products to the clinical stage, and although several assays and kits are now commercially available, many are restricted to research or investigational use only.
The great public need for improved AD detection and diagnosis, which is necessary to facilitate effective intervention, has led to the development of several public-private collaborations geared towards the large-scale validation of AD biomarkers. The largest of these efforts is the Alzheimer’s Disease Neuroimaging Initiative (ADNI), which represents a collaboration of researchers across multiple study centers who are participating in open-access and pre-competitive information sharing through the ADNI database.
These efforts are sponsored though government or public funding sources, with contributions from private industry participants that have a vested interest in developing biomarker products or AD therapies.
Collaborative efforts such as ADNI have enabled faster and more efficient advancement of AD research, and are anticipated to resolve some of the validation barriers that have limited the widespread use of biomarkers in AD.
Regulatory barriers and reimbursement hurdles impede growth of AD biomarker market
Once these biomarker assays have been developed and have gone through
the clinical trial processes required for validation, they may be ready
for clinical use, but still face regulatory barriers to market entry and
market adoption. Most countries have rigorous regulatory standards for
diagnostics, particularly the US, where the FDA requirements for the
approval of diagnostic products are very stringent, and the process
implicit in satisfying these requirements is a costly one. As such, only
products with powerful stakeholders or financial backing may be able to
successfully navigate this regulatory process. Once the products are
approved for clinical marketing, they then face the ensuing challenge of
obtaining health insurance coverage. Amyvid is a clear example of this
challenge because although it has been FDA approved since April 2012, it
is yet to be reimbursed by government or private payers, which has
greatly limited its market penetration.
Physicians and
researchers express measured optimism about the future of the AD
biomarker landscape
The key opinion leaders (KOLs)
interviewed for this report shared their insights into the current state
of the AD biomarker field: they shared the challenges impacting
biomarkers development, the unmet needs, as well the opportunities and
directions that are particularly promising for the future of this
market. The KOLs were in agreement that concerns over the
reproducibility, standardization, and ultimately the large-scale
validation of biomarkers, were key challenges in advancing biomarkers
into the clinical arena for AD. They also expressed a need for varied
biomarkers to serve needs both in AD clinical diagnosis and prognosis,
as well as to guide therapy development for AD.
“[What is needed
is] some kind of cholesterol [test] for Alzheimer’s disease, and that if
we consistently reduce cholesterol levels, we know that we are going to
consistently reduce morbidity and mortality from heart attacks. That’s
what ADNI and all these related long-term biomarker studies are really
going to enable us to do in the long run, and I think that is why they
are worth the investment — that we are going to be able to link these
biomarkers in the pre-symptomatic or mildly symptomatic stage to
longer-term outcomes, and we are going to be able to say, let’s say that
at least 90% of people who had this biomarker when they were
asymptomatic were going on to get Alzheimer’s disease within 10 years.”
[US] KOL, March 2013
“None of the biomarkers has so far been
validated as a surrogate outcome. This is what drug companies in all
likelihood would like to have because that would allow them to save a
lot of time and resources because they could do Phase II and Phase III
trials of smaller size, of let’s say 30 to 40 patients instead of 250,
as you must have now, or more, actually. So this is a big, big unmet
need.”
[EU] KOL, May 2013
The KOLs also reiterated that the
market potential of these biomarker-based tools was largely tied to the
successful development and approval of disease-modifying therapies for
AD. However, they cautioned that the absence of such treatments should
not be a deterrent for companies developing these biomarker assays
because it will be important for these companies to establish themselves
and their products in the market to ensure that they are strategically
poised prior to these drug approvals.
“These [biomarkers] will
all penetrate the market within the next one to five years, and
obviously, it would be a major boost in motivation as well as
application, if there would be an approved disease modifier.”
[EU]
KOL, April 2013
“If somebody is a major player, has an interest
in there, the market is still young, the opportunity and the potential
is still there, the commercial value is there and the medical ethical
value is there. You have to organize and coordinate that process with
your product — I think that’s successful if sustained — and then not
wait until a disease modifier becomes available because others will
penetrate the market before you, and that will be a big disadvantage.”
[EU] KOL, April 2013
See the research report: PharmaFocus: Biomarkers in Alzheimer’s Disease (on GlobalData)