CORDIS proporciona enlaces a los documentos públicos y las publicaciones de los proyectos de los programas marco HORIZONTE.
Los enlaces a los documentos y las publicaciones de los proyectos del Séptimo Programa Marco, así como los enlaces a algunos tipos de resultados específicos, como conjuntos de datos y «software», se obtienen dinámicamente de OpenAIRE .
Resultado final
Determine barriers and motivators towards uptake of on-demand and injectable PrEP
Dissemination and exploitation plan (se abrirá en una nueva ventana)Report of roles (se abrirá en una nueva ventana)
Confirmation of leadership and mentorship roles
Capacity strengthening plan (se abrirá en una nueva ventana)Study initiation package (se abrirá en una nueva ventana)
Registration number of the clinical study in a registry meeting WHO Registry criteria. Final version of study protocol as approved by the regulator(s) / ethics committee(s). Regulatory and ethics (if applicable, institutional) approvals required for the enrolment of the first study participant.
Rapid assessment and other qualitative data collection (se abrirá en una nueva ventana)Characteristics of men willing to take oral versus injectable PrEP
Draft stewardship plan (se abrirá en una nueva ventana)Beneficiaries must prepare stewardship plans outlining how to achieve the optimal use of an intervention, including, for example, how to avoid irrational use, overuse or abuse of health technologies (e.g. antimicrobials). A draft plan must be submitted after half the duration of the project has elapsed and a final plan must be submitted with the final report.
Midterm recruitment report (se abrirá en una nueva ventana)Midterm recruitment report. This report is due when 50% of the study population is recruited. The report shall include an overview of the number of recruited participants by clinical sites, any problems in recruitment and, if applicable, a detailed description of implemented and planned measures to compensate for any incurred delays. The Global Health EDCTP3 Joint Undertaking reserves the right to terminate the MOBILE MEN project if milestone MS16 has not been achieved and by month 18 no clinical trial participant has received long-acting cabotegravir.
Rapid assessment (se abrirá en una nueva ventana)Characterize mobile men at risk of HIV
Consortium meeting (se abrirá en una nueva ventana)Kick-off meeting and confirmation of committees
Newsletter to researchers and stakeholders
Launched Project Website (se abrirá en una nueva ventana)Launch of the project website.
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