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home > ebr > spring 2002 > therapeutic vaccines for hiv-1 infection - past, present and future
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European BioPharmaceutical Review

Therapeutic Vaccines for HIV-1 Infection - Past, Present and Future

The introduction of triple drug combination therapy (highly active antiretroviral therapy, or 'HAART') has had a significant impact on the morbidity and mortality of HIV-1 infection. However, initial optimism regarding the potency of antiretroviral agents was subsequently dampened when it became clear that there were still major obstacles to overcome. Undesirable side effects frequently occur and drug-resistant viruses may emerge if adherence to strict regimes is not maintained. Patients are committed to staying on therapy for life, yet it is unlikely that HIV-1 eradication can be achieved by HAART because of a persistent cellular reservoir of virus. Perhaps the most significant limitation of HAART is its cost: 90 per cent of the 40 million individuals living with HIV-1 infection today live in developing countries and have no access to treatment.


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By Dr Lucy Dorrell, Clinician Scientist Fellow at the Medical Research Council's Human Immunology Unit

Lucy Dorrell is a Clinician Scientist Fellow at the Medical Research Council Human Immunology Unit, Warrell Institute of Molecular Medicine in Oxford, UK. She is a Principal Investigator in clinical trials of novel therapeutic vaccines for HIV.
Lucy joined the Unit in 1997 and undertook research into cellular immune responses to HIV, based at MRC Laboratories, The Gambia. Prior to this she spent four years at Imperial College School of Medicine, where she took her doctorate degree, and was involved in clinical trials of antiretroviral therapies.

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Dr Lucy Dorrell
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4th Annual Patient Recruitment and Retention in Clinical Trials

13-15 October 2008, Amsterdam

Patient recruitment is now consuming thirty percent of clinical trial time - more time than any other clinical trial activity - and almost half of all trial delays result from patient recruitment problems. As the recruiting culture becomes more sophisticated and the forces affecting patient enrollment grow more numerous and complex, pharmaceutical companies are striving to discover new strategies to facilitate enrollment in clinical trials. With increasing industry pressure to develop, test and market greater numbers of new drugs faster, pharmaceutical companies need to perform clinical trials as quickly as possible. Inefficient patient recruitment processes is a formidable barrier to pharmaceutical companies' success in launching new products. Improving the patient recruitment process is imperative to avoid wasted investments and eliminate costly delays in bringing new drugs to market -- today and even more so in the not-so-distant future. Improved patient recruitment presents one of the largest opportunities for pharmaceutical companies to eliminate delays in clinical trials, thereby making it possible to reduce time to market.  With patent time limits and large overheads meaning that any delays in the development timeline can be disastrous, a good understanding of how to successfully recruit patients for trials is vital for any company looking to succeed.
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“PACK DIFFERENT” with EMBALLAGE 2008

“Business, Innovation, Outlook” are the watchwords for the 38th World Packaging Exhibition which opens in Paris from 17 to 21 November 2008. Fifteen months before the key packaging event of the end of 2008, EMBALLAGE displays its differences to offer you a new edition that is even more representative, international and rich in new features.
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