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Hit enter to return to the slide.SUBMIT ALLsubmit allQuestion ListMore infoSend an emailCloseBioExit<html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The process of recruiting participants into a clinical trial in order to reach target participant numbers.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The most severe manifestation of infection with HIV, characterized by deterioration of the immune system and susceptibility to a range of opportunistic infections and cancers.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A person or group who acts on the behalf of a cause in order to bring about change.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An unwanted effect experienced by a participant in a clinical trial. This may or may not be related to the product or procedure being studied.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A person or group who advocates on the behalf of individuals, groups, or a specific cause.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A drug or medication that acts against or suppresses a retrovirus such as HIV.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An international, non-profit organization that uses education, policy analysis, advocacy, and a network of global collaborations to accelerate the ethical development and global delivery of AIDS vaccines, male circumcision, microbicides, PrEP, and other emerging HIV prevention options as part of a comprehensive response to the pandemic.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A clinical trial that aims to discover safe and effective products or procedures to prevent HIV transmission.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A clinical trial designed to prevent the participants, research teams, or both, from knowing which participants are in the experimental arm or group and which are in the control arm or group of a trial, in order to reduce bias.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A research study that uses human volunteers to answer specific questions about the safety, efficacy or effectiveness, and medical effects of a specific procedure, medication, product, or treatment. A clinical trial process may include Phases I, II, IIb, II, and IV (post-marketing evaluation).</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Boards or groups composed of individuals or stakeholder representatives that act as an independent advisory voice and facilitate community stakeholder participation and involvement in the research process. They meet regularly with research team representatives, inform community stakeholders about proposed and ongoing research, and provide feedback to research teams about local norms and beliefs, as well as local views and concerns that arise in specific trials.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Groups of individuals who come together to act on behalf of common interests, goals, and values but whose organization does not require formal designation or registration.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Individuals and groups who are ultimately representing the interests of people who would be recruited to or participate in a clinical trial, and others locally affected by a trial. Examples of “community stakeholders” are the population to be recruited, trial participants, people living in the area where the research is conducted, people living with HIV in the area, local HIV-positive groups or networks people in the area affected by the HIV epidemic, local non-governmental organizations, community groups, and community-based organizations.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A public or private not-for-profit group (including a church or religious entity) that is representative of a community or a significant segment of a community, and is engaged in meeting human education, environmental, or public health or safety community needs, often organized as close possible to the individuals it serves.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The principle that protects the rights of trial participants regarding prevention of unauthorized disclosure of personal information to third parties during data collection, storage, transfer, and use.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The group of participants in a clinical trial who receive the placebo or control product or procedure.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An independent committee established by a trial sponsor to assess, at intervals, the progress of a clinical trial, safety data, and critical efficacy or effectiveness endpoints. A data and safety monitoring board may recommend to the sponsor that a trial be stopped or modified if there are safety concerns, if trial objectives have been achieved, or if assessment of trial progress reveals that continuing the trial would be futile since it will no longer be possible to answer the research question that the trial is addressing.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Activities required for the development, planning implementation, and conclusion of a trial including analysis and dissemination of trial results.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>In clinical research, the ability of a test product or procedure to produce a desired clinical effect.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The group of participants in a clinical trial who receive the procedure, product, or drug being studied.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A pouch, that when inserted in the vagina before vaginal intercourse, provides protection against most sexually transmitted infections, including HIV and pregnancy. During anal sex, the female condom, when placed on the penis after removing the inner ring, provides protection against most sexually transmitted infections including HIV. Currently made of polyurethane or synthetic latex, it is stronger than the natural latex used in male condoms, odorless, non-allergenic, and usable with oil-based lubricants. For vaginal intercourse, it can be inserted vaginally prior to intercourse, is not dependent on male erection, and does not require immediate withdrawal after ejaculation.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Activities that enable research teams to gain an informed understanding of local populations, sociocultural norms and practices, local power dynamics, local perceptions, channels of communication and decision-making, and local history of research, as well as the needs and priorities of people locally affected by or able to influence a clinical trial. Formative research activities usually constitute the initial phase of stakeholder outreach and engagement.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The inability of a clinical trial to achieve one or more of its objectives. This determination may be suggested, for example, during an interim analysis of a trial by a data safety monitoring board.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Guidelines that set a standard for compliance by laboratories involved in the analysis of samples from clinical trials. These guidelines provide guidance to ensure that trial laboratory data are reliable, repeatable, auditable, and easily reconstructed in a research setting.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Internationally recognized guidelines for designing, conducting, recording, and reporting clinical trials in which humans participate. GCP provides guidance to ensure that trial data are credible and to protect the rights, safety, and well-being of trial participants. The guidelines were issued by the international conference on harmonization of technical requirements for registration of pharmaceuticals for human use.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Quality assurance practices that ensure that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization. Good manufacturing practices are aimed primarily at diminishing the risks inherent in any pharmaceutical or medical device production.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A vaccine designed to prevent HIV infection in HIV-negative individuals. Currently no effective HIV vaccine exists.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A process by which a competent individual voluntarily confirms his or her willingness to participate in a particular clinical trial after having been informed of all aspects of the trial which are relevant to the individual’s decision to participate. Informed consent is an ongoing process throughout the course of a clinical trial.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>UNAIDS brings together the resources of the UNAIDS Secretariat and 10 UN system organizations to lead and inspire the world in achieving universal access to HIV prevention, treatment, care, and support.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A sheath designed to be worn over the penis during vaginal, anal, or oral intercourse as a means of preventing sexually transmitted infections, including HIV, or preventing pregnancy in the case of vaginal intercourse.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The surgical removal of the entire foreskin of the penis. Three clinical trials conducted in sub-Saharan Africa have shown that medically performed male circumcision is safe and can reduce men’s risk of HIV infection during vaginal sex by about 60%. Prevalence of male circumcision varies by geography, religion, and cultural practices.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Men who have sexual contact with other men regardless of whether or not they also have sex with women or have a personal or social gay or bisexual identity. This concept also includes men who self-identify as heterosexual but have sex with other men.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A range of products that could be used vaginally or rectally (such as a gel, cream, ring, film, suppository, or sponge) that are being tested to determine if they reduce or prevent the transmission of HIV and other disease-causing organisms during vaginal and anal intercourse.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A not-for-profit registered entity or group that is organized on local, national, or international levels but is not an agency of local or national governments.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An inactive substance that is designed to appear like an experimental product being studied in all aspects expect for the absence of the active ingredient under study. In clinical trials, the safety and effectiveness of an experimental product are assessed by comparing data from the experimental product trial arm to those from the placebo arm.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Antiretroviral medicines prescribed and taken soon after exposure or possible exposure to HIV, to reduce the risk of acquiring HIV. The exposure may be occupational, as in a needle stick injury, or non-occupational, as in the case of rape.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Antiretroviral drugs used by a person who does not have HIV infection to be taken before possible exposure to HIV in order to reduce the risk of acquiring HIV infection.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The specific study product or procedure, such as the experimental or ‘active’ arm or the placebo arm, to which a participant is assigned for the designated follow-up period.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A document that details the rationale, goals, design, methodology, statistical considerations, and organization of a study or clinical trial. A protocol describes a scientific study designed to answer specific research questions and describes how the health of the trial participants will be safeguarded.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A method based on chance alone by which trial participants are assigned to a trial arm or group. Randomization ensures that the only intended difference between trial arms or groups is which product or procedure a trial participant is exposed to during the trial.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A clinical trial in which participants are assigned by chance to one of the trial arms or groups.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Government agencies charged with carrying out the intent of legislation that constrains the actions of private individuals, businesses, organizations, institutions, or government bodies. In most countries one or more regulatory agencies may be responsible for ensuring the safety and effectiveness of health products and the correct conduct of clinical trials.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An independent body made up of medical, scientific, and non-scientific members whose responsibility is to protect the rights, safety, and wellbeing of human participants involved in a clinical trial. Research ethics committees review and approve the initial protocol review materials to be used in recruiting and consenting trial participants, and provide continuing review of a trial protocol and any amendments. The term “institutional review board” is common in the United States of America, whereas other countries commonly use the term “research ethics committee” or “independent ethics committee”.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A cooperative of research institutions or centers conducting clinical trials under a common research agenda.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A group of investigators and staff involved in implementing biomedical HIV prevention trials. Research teams can include investigators and staff working at coordinating centers, institutions, or agencies.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A recognized systematic way to form and test hypotheses by designing controlled experiments to collect data, analyze results, and draw conclusions in order to acquire new knowledge or to correct, refine, and integrate previous knowledge.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The process by which a newly infected person develops antibodies that can be detected by an HIV antibody test. Development of antibodies may occur anywhere from weeks or months following HIV infection.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Infections caused by microorganisms that are transmitted from one person to another during sexual or intimate contact.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Processes through which trial funders, sponsors, and implementers build transparent, meaningful, collaborative, and mutually beneficial relationships with interested or affected individuals, groups of individuals, or organizations with the ultimate goal of shaping research collectively.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Individuals, groups, organizations, governments, or other entities that are affected by the outcome of a biomedical HIV prevention trial or that can influence proposed research through their input and actions.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A document that gives step-by-step instructions for how to conduct a procedure, in order to ensure that each staff member can perform the procedure in the same way.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A pattern of prejudice, discounting, discrediting, and discrimination directed at people perceived to have HIV or AIDS, their significant others, and close associates or their social groups.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An antiretroviral drug that decreases the amount of HIV in the blood by inhibiting (or blocking) the replication of the virus. Tenofovir is sometimes used alone or in combination with other antiviral medications. Marketed by Gilead under the brand name Viread for HIV treatment, It is also being tested for prophylactic use to prevent infection among uninfected individuals, an intervention generically known as PrEP.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A compound designed to stimulate the immune response to HIV in a person already infected with the virus in order to control the infection. Also referred to as an immunotherapeutic vaccine.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A person who identifies with or expresses a gender other than their sex assigned at birth or biological gender. Transgender woman refers to a person who identifies as a female but was assigned a “male” sex at birth.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A group within a clinical trial formed of participants who have been assigned a particular product or procedure during a trial.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An individual or entity responsible for financing the cost of a trial.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>Investigators, research staff, and all others specifically responsible for executing biomedical HIV prevention trials. Implementers may be employed by governments, government-sponsored networks, non-governmental organizations, academic institutions, the pharmaceutical industry, or other companies, foundations, or public private partnerships.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The entire process of a trial, starting from developing the initial concept and writing the protocol and continuing through to the implementation and conduct of the trial to completion, exiting of participants, and dissemination and reporting of results.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A competent individual who voluntarily provides informed consent to participate in a clinical trial. Trial participants are assigned to particular trial arm or group, in which they receive a particular product or procedure.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>An entity that is responsible for a trial but that does not actually conduct it. The sponsor may be a pharmaceutical company, governmental agency, academic institution, or private or other organization.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The process of revealing trial participants’ product or procedure assignments. Unblinding involves informing participants about which product they were assigned to during the trial.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>A compound that stimulates the body’s immune response in order to prevent or control an infection. A vaccine is typically made up of parts of a bacterium or virus that cannot itself cause an infection.</textformat></html><html><textformat leading='0' tabstops='[0, 48, 96]' blockindent='0' indent='0'>The WHO is the directing and coordinating health organization within the United Nations. The organization sets standards and articulates evidence-based policy options for HIV/AIDS treatment and prevention.</textformat></html>