Até o final de agosto, 400 homens serão escolhidos para participar dos testes. Os estudos deverão ser finalizados em 2016. Se os resultados obtidos forem satisfatórios, servirão para auxiliar o governo quanto à adoção permanente para uma terapia preventiva, como acontece nos Estados Unidos.
Associação tenofovir/emtricitabine
| Associação tenofovir/emtricitabine Alerta sobre risco à saúde |
|
|---|---|
| Identificadores | |
| Número CAS | |
| PubChem | |
| Código ATC | J05 |
| Farmacologia | |
| Via(s) de administração | Oral |
| Classificação legal |
POM (UK) ℞-only (US) |
| Riscos na gravidez e lactação |
B (EUA) |
| Excepto onde denotado, os dados referem-se a materiais sob condições PTN Referências e avisos gerais sobre esta caixa. Alerta sobre risco à saúde. |
|
Sob o nome comercial Truvada, do laboratório farmacêutico Gilead Sciences, nas formas farmacêuticas gel ou pílula,1 foi aprovada nos Estados Unidos pela Food and Drug Administration em 2004.
Em novembro de 2010 foi anunciado que a combinação de medicamentos pode reduzir em 44% o risco de contaminação em homens. No caso, o medicamento é ingerido antes da contaminação, como forma de prevenção em pacientes de grupo de risco.2
Em julho de 2012, a FDA (agência do governo norte-americano que regula remédios e alimentos no país) anunciou a aprovação do Truvada como pílula preventiva para pessoas não contaminadas pelo vírus da AIDS, inicialmente para pessoas que convivem em grupos de risco, como prostitutas e parceiros sãos de pacientes infectados.3 4
A combinação contendo Truvada e efavirenz (Sustiva) é também conhecida pela marca Atripla.
HIV-prevention pill endorsed by U.S. health officials
Food and Drug Administration backs Truvada tablet for those at risk of infection
The Associated Press
U.S. federal drug regulators affirmed landmark
study results showing that Truvada, a popular HIV-fighting pill, can
also help healthy people avoid contracting the virus that causes AIDS in
the first place. (Gilead Sciences/Associated Press)
In a series of votes, a Food and Drug Administration advisory panel recommended approval of the daily pill Truvada for healthy people who are at high risk of contracting HIV, including gay and bisexual men and heterosexual couples with one HIV-positive partner.
Daily
doses of Truvada, already used to treat HIV infections, helped prevent
healthy gay men and transgendered women from acquiring the disease
through sex with an infected partner, according to an international
study. (Paul Sakuma/Associated Press)The FDA is not required to follow the panel's advice, though it usually does. A final decision is expected by June 15.Gilead Sciences Inc., based in Foster City, Calif., has marketed Truvada since 2004 as a treatment for people who are infected with the virus. The medication is a combination of two older HIV drugs, Emtriva and Viread. Doctors usually prescribe it as part of a drug cocktail to repress the virus.
While panelists ultimately backed Truvada for prevention, Thursday's 12-hour meeting highlighted a number of concerns created by the first drug to prevent HIV. In particular, the panel debated whether Truvada might lead to reduced use of condoms, the most reliable defence against HIV. The experts also questioned the drug's effectiveness in women, who have shown much lower rates of protection in studies.
Panelists struggled to outline steps that would ensure patients take the pill every day. In clinical trials, patients who didn't take their medication diligently were not protected, and patients in the real world are even more likely to forget than those in studies.
Patients could develop resistence to drug
"The trouble is adherence, but I don't think it's our charge to judge whether people will take the medicine," said Dr. Tom Giordano of Baylor College of Medicine, who voted in favour of the drug. "I think our charge is to judge whether it works when it's taken and whether the risks outweigh the benefits."Panelists stressed that people should be tested to make sure they don't have HIV before starting therapy with Truvada.
Patients who already have the virus and begin taking Truvada could develop a resistance to the drug, making their disease even more difficult to treat. The experts grappled with how to protect patients while avoiding hurdles that could discourage them from seeking treatment.
"If we put up too many hoops to jump through, there will be people who don't make it through those hoops," said Daniel Raymond, the panel's patient representative.
Truvada first made headlines in 2010, when government researchers showed it could prevent people from contracting HIV. A three-year study found that daily doses cut the risk of infection in healthy gay and bisexual men by 42 per cent, when accompanied by condoms and counseling. Last year another study found that Truvada reduced infection by 75 per cent in heterosexual couples in which one partner was infected with HIV and the other was not.
FDA approval would allow Gilead Sciences to formally market its drug as a preventive measure.
The drug needs to be approved by regulators for prevention before Canadian doctors could ethically prescribe it as a preventive to uninfected individuals, said Dr. Mark Wainberg, director of the McGill AIDS Centre in Montreal.
False sense of security
'Truvada needs to be taken every day, 100 per cent of the time, and my experience as a registered nurse tells me that won't happen'—Karen HaugheyBut Truvada's groundbreaking preventive ability has exposed stark disagreements on prevention among those in the HIV community. While Truvada's supporters say the drug is an important new option, critics worry that the drug could give users a false sense of security, and encourage risky behavior.
During the meeting's public comment period, FDA panelists heard from more than two dozen doctors, nurses and patients who said patients would not take the drug as recommended — every day, in addition to using condoms.
"Truvada needs to be taken every day, 100 per cent of the time, and my experience as a registered nurse tells me that won't happen," Karen Haughey told the panel. "In my eight years, not one patient that I've cared for has been 100 per cent adherent."
Wainberg is organizing a placebo-controlled trial to test giving Truvada to those at high risk of infection without the daily dosing requirement.
"In Canada we actually want to do a study that would … not give drug every day to people but give the drug only in advance of the day of the week when they anticipate having relations," Wainberg said in an interview.
If a gay man participating in the study knows he's going out only on Friday night then he'd be instructed to dose himself the morning before and perhaps the day after and use a condom, but not take Truvada the other five days.
"We're hoping that [the study] will get off the ground pretty soon."
Other speakers worried that wide-scale use of Truvada would divert limited funding from more cost-effective options. Truvada sells for about $900 a month, or just under $11,000 per year. The AIDS Healthcare Foundation, which opposes approval of Truvada, estimates that 20 HIV-positive patients could be treated for the cost of treating one patient with preventive Truvada.
"Truvada for prevention will squeeze already-constrained health care resources that can be better spent on cheaper and more effective prevention therapies," the group states in a petition to the FDA.
© The Associated Press, 2012
Outras notícias
O jornal O Globo publicou, em seu site, uma matéria com alguns esclarecimentos sobre Doenças Sexualmente Transmissíveis (DSTs), HIV e Aids. Clique aqui e leia a matéria.
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