Spanish vaccine volunteer says: ‘For me the real risk is that people aren’t vaccinated’
Ezequiel Martín is a 46-year-old computer specialist from Málaga, but has been living in London for more than 10 years. When the coronavirus pandemic broke out, he, like many others, tried to read as much information about what was happening, and it was during this research that he saw that volunteers were needed for the trial of the vaccine being developed by Oxford University and the British-Swedish drug company AstraZeneca.
The Spanish government is set to receive 31 million doses of this vaccine, as part of a deal struck by the EU. On the back of this news, Spanish Prime Minister Pedro Sánchez said last Monday that: "We hope to begin vaccinating part of the population of Spain in December," with the initial three million doses the country is set to receive.
But last Tuesday, September 8th, a spokesperson for AstraZeneca announced that the Phase 3 trial had been put on hold, after one of the participants fell ill. In an in interview with El Pais, Ezequiel explained that despite the bad news he is still eager to take part in the trial, and on Saturday, Oxford University announced that the trial had been deemed safe to continue again.
Q: What did you think when you found out that a volunteer had been hospitalized and the trials suspended?
A: I think that it is one person among the nearly 100,000 of us who have already received the vaccine. It doesn’t seem like a lot, it’s an acceptable risk. We are talking right now about reopening the world, as they say. For me, the real risk is that people are not vaccinated and that we are all still going out on the street.
Q: Are you still committed to taking part in the trial?
A: Yes, of course. As soon as they resume the trial, they have already said they are going to call me again to fix a date for the second vaccine (he received the first shot in June), and I will be there.
Q: What did your wife say when you decided to sign up?
A: That this is just like me, that I sign up to everything. It’s true that I never thought of it as something risky, as it was Phase 3. They had already done safety studies and given it to lots of people, but when I mentioned it to her and other friends, the reaction of most of them was: "Oh, don’t you think that’s dangerous?" What’s funny is that I rushed to sign up because I thought for sure that everyone would want to do it.
Q: Did they warn you of any risks?
A: Yes, at the beginning they sent me a lot of paperwork and a lot of information about the possible side effects. Some were very normal, like I was going to have a fever and that my arm would hurt for a few days, but in the end, nothing happened to me, although they wanted to be sure. They also spoke to me about other, more serious effects, possible rare diseases, but they made it clear that the likelihood was low, one in 10,000 cases. They assured me that I would be kept up to date at all times, and were wonderful with their explanations.
Q: How did you find out about the situation with the volunteer?
A: They called me up personally, before it made the news. It happened just as I was waiting for the call for the second meeting. They told me that there was a case of a person who had had something, and that the process was suspended while they investigated what had happened. It was something, to be sure, that they had explained to be before I was made aware of the protocol.
Q: And do you trust them?
A: Yes, a lot. The first tests were done in the University College Hospital in London, where my daughter was born. They are very serious and that gave me a lot of security, I know that they have been doing a lot of research there for a long time.
Q: Do you think the trial will be successful?
A: Yes, because what is happening right now is what they said was going to happen, according to the forecasts. No one at any time said that this was going to be a miracle cure that would make the disease disappear, but it seems like they are moving very quickly. It won't be perfect, or a complete barrier so that you can go outside and do anything you want.
Q: How long have you committed for?
A: One year. If everything goes like they think it will, there will still be time to make everyone happy, but they told me that, if the figures were good, they would end it earlier, and at that time, they would tell us if we were in the control group or in the study (which received the vaccine candidate and not the placebo). If I was in the control group, they would offer me the chance to have the vaccine at that very moment.