Title: Disease Overview:Alzheimers Disease-Identifying and Commercializing Market
1Frontier Pharma Alzheimers Disease-Identifying
and Commercializing Market
2DESCRIPTION
Large and Innovative Pipeline The active
Alzheimers Disease (AD) pipeline is populated
with 583 products, with a highly diverse range of
molecular targets. GBI Research analysis revealed
a high degree of innovation in this indication,
with 46 of the pipeline being first-in-class
products, acting on over 40 first-in-class
molecular targets. In addition, the pipeline is
characterized by the strong presence of therapies
that target multiple components implicated in the
amyloid cascade, several molecular targets of
which are known to trigger familial AD. Given
that the currently approved therapies for AD are
limited to acetyl cholinesterase inhibitors and
glutamate receptor antagonists, the pipeline
offers a broad range of treatment options that
may possess disease-modifying properties.
However, evaluation of the Preclinical and
clinical evidence for their therapeutic potential
reveals that the novelty of the molecular target
is not sufficient to effectively reduce the rate
of AD progression in human patients.
3Report Description
- Disease-Modifying Therapies Show Promise in
Early-Stage Development - Programs undergoing Preclinical development
exhibit diverse disease-modifying mechanisms of
action, and many represent strong alternatives to
targets with a direct role in the amyloid and tau
processes due to their roles in promoting
neuronal survival and plasticity, a process
critical to memory and cognition. Brain-Derived
Neurotrophic Factor (BDNF) and Nerve Growth
Factor (NGF) are considered promising targets in
AD, primarily due to their potency in exhibiting
significant neuroprotective effects in
Preclinical studies. Members of the
caspase-mediated apoptotic cascade also show
therapeutic potential, as early investigations
have revealed an ability to modulate molecular
mechanisms underlying synaptic plasticity in
animal models, which translates into amelioration
of behavioral deficits. Thus, growing insights
into disease-causing processes in AD are being
translated into a growing population of
innovative therapeutic targets, as reflected in
the highly innovative pipeline.
4Key Segment
- The merits of novel molecular targets depend
largely on the body of Preclinical evidence
underpinning their relevance to AD pathology.
Many endpoints in Preclinical investigations
focus on amelioration of amyloid burden and tau
pathology, as well as cognitive performance in
animal model systems. - Based on these assessment criteria, it appears
that programs targeting the amyloid cascade, tau
pathology, and the promotion of neuronal survival
and plasticity all demonstrate promising efficacy
profiles. Other first-in-class targets that are
less directly aligned to these three processes
may not be able to confer disease-modifying
properties and therefore lack clinical and
commercial potential. - Read The Complete Report On http//www.bigmarket
research.com/frontier-pharma-alzheimers-disease-id
entifying-and-commercializing-first-in-class-innov
ation-market
5Key Market
- Active Deals Landscape with Numerous Investment
Opportunities - The AD deals landscape has been highly active
over the past eight years, with 83 licensing
agreements and 103 co-development deals. Overall,
non-first-in-class programs tend to have lower
valuations than first-in-class programs across
all stages of drug development, which highlights
their commercial attractiveness, even in
early-stage development. Although first-in-class
programs are associated with greater risk, they
have more potential to revolutionize or improve
therapeutic options, meaning that identifying
promising first-in-class compounds early in
development offers the greatest potential
commercial benefit to pharmaceutical companies. - With 153 first-in-class products that are
currently in development having not yet been
involved in a licensing or co-development deal,
there are numerous opportunities for in-licensing
or co-development in this indication.
6SCOPE
- The report covers and includes
- A brief introduction to AD, including symptoms,
pathophysiology, and overview of pharmacotherapy
and treatment algorithms - The changing molecular target landscape between
market and pipeline and particular focal points
of innovation in the pipeline - A comprehensive review of the pipeline for
first-in-class therapies, analyzed on the basis
of stage of development, molecule type and
molecular target - Identification and assessment of first-in-class
molecular targets with a particular focus on
early-stage programs for which clinical utility
has yet to be evaluated, as well as literature
reviews of novel molecular targets - Assessment of the licensing and co-development
deal landscape for AD therapies and benchmarking
of deals involving first-in-class versus
non-first-in-class-products
7REASONS TO BUY
- The report will assist business development and
enable marketing executives to strategize their
product launches, by allowing them to - Understand the focal shifts in molecular targets
in the AD pipeline - Understand the distribution of pipeline programs
by phase of development, molecule type and
molecular target - Access a scientific and clinical analysis of
first-in-class developmental programs for AD,
benchmarked against non-first-in-class targets - Access a list of the first-in-class therapies
potentially open to deal-making opportunities - To Get More Details Enquire _at_ http//www.bigmarket
research.com/report-enquiry/176585
8 Table Of Content
- Executive Summary
- The Case for Innovation
- Clinical and Commercial Landscape
- Clinical and Commercial Landscape
- Assessment of Pipeline Product Innovation
- Liver Cancer Patent Family Analysis
- Signaling Network, Disease Causation and
Innovation Alignment - First-in-Class Target Evaluation
- Deals and Strategic Consolidations
- Appendix
- Read The Complete TOC _at_ http//www.bigmarketresear
ch.com/frontier-pharma-alzheimers-disease-identify
ing-and-commercializing-first-in-class-innovation-
market
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