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On this International Women’s day 2012 we would like to send out special thanks to all the volunteers in Mucovac 2 

by:

Sarah Joseph posted on 08/03/2012 at 15:00

The trial is going full steam ahead. As of this week, we are approaching halfway - 13 women have been recruited into the trial and things are going very well. It seems as though the rate of recruitment is accelerating which is terrific news. Without healthy volunteers like you, none of this research would be possible and we appreciate your commitment very much.

It has been almost a year since I have updated my blog and I can’t believe how the time has flown by. A lot has been happening in the world of HIV vaccines. September 2011 saw the annual HIV vaccine conference in Bangkok which is one of the main events in the calendar for those working in the field. The location was particularly relevant because some hotly anticipated results from the RV144 were the highlight of the meeting. I mentioned the RV144 or “Thai trial” in my previous blog. The vaccine did not work well enough to be taken further in its present form but the encouraging results provided new impetus to the field and also, potentially, clues as to how the vaccine might be having its effect. After extensive analysis of the samples carried out in a spirit of unprecedented collaboration, two of the responses made to the vaccine turned out to be important in determining whether a volunteer got infected with HIV (see below for more information). The results are of particular interest to us because we are currently in the final stages of planning two trials which follow a similar vaccination strategy to the one used in RV144. The UKHVC003 trial will start later in 2012 in London and the Tamovac 01 trial is already running in Tanzania and Mozambique. Based on our previous results, we think that some responses that we will see to the vaccines in these trials might be better than those seen in RV144. We will have to wait and see whether the immune responses which develop after vaccination are similar to those that showed a relationship to protection from infection in the Thai trial. We have no way of knowing whether this will be the case until we have finished the trial.

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Sarah Joseph works in the area of HIV prevention at the
Medical Research Council Clinical Trials Unit


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Why have we set up this website?

One of the main reasons that clinical trials ‘fail’ is because they don’t recruit as many volunteers as needed before the money runs out or the product being tested expires. We have struggled with almost all the healthy volunteer studies that we have been involved with in UK. 

This may be partly explained by the fact that we are investigating products to prevent HIV, and HIV is an infection that people are scared of. When people get the chance to speak to us, we can usually address their concerns as these invariably arise from misconceptions.

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In 1983 the virus causing HIV was first identified, 2 years after the first patients with AIDS were described in the scientific literature. By 1984 there was a reliable test that, if positive, meant an individual had acquired HIV.  It was already suspected that AIDS was transmitted through body fluids, but having the test helped to confirm this and to create a clearer picture of who was at high risk, and which countries had the highest proportion of positive individuals.

Today, the global burden of HIV is greatest in sub-Saharan Africa and these countries are struggling to deliver treatment and care to an ever increasing number of HIV positive individuals.

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Anyone who considers themselves healthy can join the network.

Every trial will have specific criteria that define who can and who can’t take part, and these are in place mainly to ensure the safety of participants. There are a few that apply to all trials in healthy voluinteers.

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