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Crucell corporate brochure (PDF)

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14<br />

Our business – Research and development<br />

Our strong research and development pipeline<br />

Innovation is the driving force behind <strong>Crucell</strong>’s future growth supported<br />

by a strong R&D pipeline. Our scientists focus on the discovery and<br />

development of much-needed solutions for major threats to human<br />

health—particularly vaccines and antibodies for the prevention and<br />

treatment of infectious diseases. This has resulted in a broad pipeline<br />

of investigational products with the potential to revolutionize the fight<br />

against diseases such as influenza, rabies, malaria and tuberculosis.<br />

Vaccine development: based on AdVac® technology<br />

AdVac® technology involves the use of novel adenoviral vectors, such<br />

as Ad35 and Ad26, in vaccines for diseases caused by viruses, bacteria<br />

or parasites. These vectors are harmless adenoviruses that have been<br />

disabled so that they cannot replicate. A vector functions as an efficient<br />

‘gene taxi’, delivering into the human body a fragment of DNA that<br />

carries the code for a protein of a specific pathogen. Once inside the<br />

body, the vectors express (produce) these proteins and present them<br />

to the person’s immune system, which mounts its protective response.<br />

Using this versatile vaccine vector platform in combination with our<br />

PER.C6® manufacturing technology, we are working with our partners<br />

to develop vaccines against major threats to human health, including<br />

tuberculosis, malaria, Ebola and Marburg, HIV, human papilloma virus<br />

(HPV) and respiratory syncytial virus (RSV). See page 17.<br />

Tuberculosis (Phase II)<br />

<strong>Crucell</strong> joined forces with the nongovernmental organization (NGO)<br />

Aeras Global TB Vaccine Foundation in 2004 to develop a safe, effective<br />

and affordable vaccine against tuberculosis (TB). The traditional TB<br />

vaccine developed more than 85 years ago, Bacille Calmette Guérin<br />

(BCG), does not reliably prevent pulmonary disease—the most common<br />

form of TB—so there is a great need for a better alternative.<br />

Together with Aeras, we are developing the novel TB vaccine candidate<br />

AERAS-402/<strong>Crucell</strong> Ad35. The vaccine is based on <strong>Crucell</strong>’s innovative<br />

AdVac® technology, which uses novel harmless adenoviruses as vaccine<br />

vectors (vehicles). We are using the adenovirus 35 (Ad35) vector for this<br />

particular vaccine.<br />

www.crucell.com<br />

AERAS-402/<strong>Crucell</strong> Ad35 is being designed as a ‘booster’ vaccine that<br />

will be given to people who have previously been vaccinated with<br />

the traditional TB vaccine or an improved, recombinant version of the<br />

BCG vaccine that is being developed by Aeras. The BCG vaccine will prime<br />

(prepare) the immune system to fight off TB infection and the AERAS-402/<br />

<strong>Crucell</strong> Ad35 will be given later to boost this initial immune response.<br />

Data from AERAS-402/<strong>Crucell</strong> Ad35 clinical trials (Phase I and II) support the<br />

immunogenicity and acceptable safety profile of the candidate TB vaccine.<br />

In 2009, an estimated 1.7 million people<br />

died of tuberculosis.<br />

Source: WHO, Global TB Control 2010 report.<br />

Tuberculosis<br />

Estimated new TB cases (all forms) per 100,000 population in 2009.<br />

0–24<br />

25–49<br />

50–99<br />

100–299<br />

>300<br />

No estimate

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