Summary
Breast
cancer, a malignant neoplasm, is the second most common cancer and the most
common cancer in women worldwide, accounting for 16% of all female cancers,
making the disease exceedingly prevalent. The number of women diagnosed with
breast cancer has increased over the past few decades, but the number of deaths
has declined due to earlier diagnosis and better treatment options.
Breast
cancer treatment has been revolutionized in the past four decades, especially
with increasing usage of targeted therapies. The marketed products landscape
comprises a wide range of treatment options, including hormonal therapies,
chemotherapies, combination therapies, and targeted therapies. Nevertheless, significant unmet need remains
for products that can improve overall survival rate, time to disease
progression, and overall response.
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Scope
The
current breast cancer market contains novel products, including Perjeta, a
targeted therapy; Kadcyla, a human antibody-drug conjugate; and Halaven, a
novel chemotherapeutic agent.
- What are the competitive advantages of the
existing novel drugs?
With
over 700 active pipeline molecules, most of the investigational drug candidates
are being evaluated for the first-line or second-line treatment of
advanced-stage breast cancer, featuring new combination therapies, targeted
therapies, and promising immunotherapies, as well as chemotherapy drug
candidates.
- Which classes of novel drugs are most
prominent within the pipeline?
- Is there strong potential for the pipeline
to address unmet needs within the breast cancer market?
Analysis
of clinical trials since 2006 identified that the failure rates of breast
cancer molecules were highest in Phase II (41%), with the overall attrition
rate for breast cancer in development being 61%.
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- How do failure rates vary by product stage
of development, molecule type, and mechanism of action?
- How do other factors, such as average trial
duration and trial size influence the costs and risks associated with product
development?
Over
the 2014–2021 forecast period, the breast cancer therapeutics market in the
eight major markets
is expected to increase in value at a CAGR of 7.3%, from
$10.4 billion to over $17.2 billion.
- Which markets make the most significant
contribution to the current market size?
- What are the epidemiology trends in these
markets?
- Will new market entrants lead to
substantial changes in annual therapy costs?
- How will different treatment usage patterns
impact growth in the eight major markets?
Rising
breast cancer incidence and new product approvals will lead to significant
market growth over the forecast period, despite generic sales erosion resulting
from patent expirations.
- Will patent expirations or emerging
pipeline molecules threaten the commercial success of existing drugs?
- Which patent expirations will have the most
significant impact on the market?
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Reasons to buy
This
report will enable you to -
-
Understand the clinical context of breast cancer by considering symptoms,
etiology, pathophysiology, epidemiology, diagnosis, and treatment options.
-
Identify the therapeutic strategies, products, and companies that dominate the
current marketed products landscape and recognize gaps and areas of unmet need.
-
Identify key pipeline trends in molecule type, administration route, mechanism
of action, and novelty.
-
Consider market opportunities and potential risks by examining trends in breast
cancer clinical trial size, duration, and failure rate by stage of development,
molecule type, and mechanism of action.
-
Recognize the late-stage pipeline molecules that have demonstrated strong
therapeutic potential in
breast cancer by examining clinical trial data and
multi-scenario product forecast projections.
-
Compare treatment usage patterns, annual therapy costs, and market growth
projections for the US, Canada, the UK, France, Germany, Italy, Spain, and
Japan.
-
Discover trends in licensing and co-development deals concerning breast cancer
products and identify the major strategic consolidations that have shaped the
commercial landscape.
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