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CORDIS - Resultados de investigaciones de la UE
CORDIS

RBD Dimer recombinant protein vaccine against SARSCoV2

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

Project website (se abrirá en una nueva ventana)

A specific website for the project as described in task 73 will be developed A document including screenshots and the link to the website will be generated

Interim assessment of the Project (se abrirá en una nueva ventana)

Halfway through the project an assessment of the degree of fulfilment of the objectives of the project will be carried out and reported in this deliverable

Report on the psychosocial impact (se abrirá en una nueva ventana)

A report including the assessment of the social impacts will be elaborated

Position paper in One health area (se abrirá en una nueva ventana)

Paper for policy makers and other stakeholders in the area on One health. The position paper will include recommendations for the area based in the experience of RBDCOV project.

Report on the participant's centric design protocol for RBDCOV (se abrirá en una nueva ventana)

Description of the main points that have been considered and discussed during the preparation of the protocol

Notification of first patient treated in children and adolescents clinical trial (se abrirá en una nueva ventana)
Report on a meeting with the VACCELERATE project, including concrete plan for collaboration (se abrirá en una nueva ventana)

Upon availability of clinical trial data that would allow further evaluation of the developed vaccine candidates in Phase II clinical trials RBDCOV will organise a meeting with the VACCELERATE project InfoVaccelerateEU to present their findings and seek advice on how to best make use of existing clinical trial infrastructure developed in the VACCELERATE project VaccelerateEU to accelerate further clinical development of the vaccine candidates

Final Business plan for RBDCOV (se abrirá en una nueva ventana)

A document with the final business plan will be focused on the strategy for commercialisation and exploitation of the vaccines after the end of the project. The document will also include the business plan for any other commercial result of the project.

Regulatory strategy report (se abrirá en una nueva ventana)

The regulatory report will define the regulatory pathway and milestones for the optimal development of the vaccine including also CMC preclinical and clinical aspects and considering EMA Fast track procedures

Report on communication and dissemination activities (se abrirá en una nueva ventana)

A detailed list of dissemination activities carried out halfway through the project with assessment of their impact the degree of compliance with the plan and a description of foreseen dissemination activities until the end of the projectThe report will be updated in month 24 and 30

Children and adolescents initiation package (se abrirá en una nueva ventana)

The deliverable will be submitted before the enrolment of the first participant and will include the registration number of the clinical study, final version of the study protocol (approved by regulators and ethical committees) and the copies of the document that demonstrate the approval of the trial in the correspondent sites

Children and adolescents Mid-term recruitment report (se abrirá en una nueva ventana)

A report including the number of participants included at each clinical site until the end of month 5 of the clinical trial where the achievement of the 50% participants is expected

Data Management Plan for RBDCOV project (se abrirá en una nueva ventana)

A data management plan addressing all the aspects inlcuded in the template for data management plans avaliable for Horizon Europe projects will be submitted as deliverable This DMP will be aligned with the draft included in the submission of the Grant Agreement and will be updated accordingly during the project duration

Plan for the Exploitation and Dissemination of Results (PEDR) (se abrirá en una nueva ventana)

This document will describe in detail the project communication dissemination and exploitation strategy in all of its components objectives audiences channels actions results IP management and tools

Notification of first patient treated in Variants' clinical trial (se abrirá en una nueva ventana)

Notification of first patient treated in Variants clinical trial

Report on the early engagement with the European Medical Agency (se abrirá en una nueva ventana)

A brief report on a consultation with the European Medical Agency EMA to ensure that regulatory aspects for the clinical development and evaluation of the candidate compounds are properly addressed and embedded in the study design Scientific advice and protocol assistance European Medicines Agency europaeu Requesting scientific advice or protocol assistance from EMA European Medicines Agency europaeu

Report on the status of posting results of the vaccine in children (se abrirá en una nueva ventana)

Summary of the posting results in the applicable registry.

Mid-term recruitment report of the variant vaccine (se abrirá en una nueva ventana)

A report including the number of participants included at each clinical site until the end of month 5 of the clinical trial where the achievement of the 50 participants is expected

MA&P strategy report (se abrirá en una nueva ventana)

The market access and pricing strategy for the vaccines developed by HIPRA will be described in this report including the potential risks and markets for the commercialisation with a clear OH strategy

Quality assurance guidelines and procedures (se abrirá en una nueva ventana)

A set of quality assurance principles

Report on the status of posting results of the variant vaccine (se abrirá en una nueva ventana)

A summary of the posting results in the applicable registry

Biological sample logs and database with clinical information (se abrirá en una nueva ventana)

This deliverable will account for the generation of a comprehensive database including sample information and clinical information according to the data management plan.

Toolbox with the information documents co-developed with the CAB (se abrirá en una nueva ventana)

Including info sheets, informed consent, etc.

Target communication tools (se abrirá en una nueva ventana)

How to communicate complex information into a laymans language Infographics among other tools will be summarised in the deliverable

Final assessment of the project (se abrirá en una nueva ventana)

At the end of the project, a final assessment of the degree of fulfilment of the objectives of the project.

Data Management Plan regarding clinical data (se abrirá en una nueva ventana)

Includes details around database workflows external vendors requirements for reconciliations and details surrounding planned formal analyses including final database lock

Derechos de propiedad intelectual

BIMERVAX HIPRA

Número de solicitud/publicación: EU 018704530
Fecha: 2022-05-17
Solicitante(s): LABORATORIOS HIPRA SA

BIMERVAX

Número de solicitud/publicación: EU 018704520
Fecha: 2022-05-17
Solicitante(s): LABORATORIOS HIPRA SA

SARS-COV-2 SUBUNIT VACCINE

Número de solicitud/publicación: 20 22060941
Fecha: 2022-04-25
Solicitante(s): HIPRA SCIENTIFIC SL

SARS-COV-2 SUBUNIT VACCINE

Número de solicitud/publicación: 20 22060941
Fecha: 2022-04-25
Solicitante(s): LABORATORIOS HIPRA SA

SARS-COV-2 SUBUNIT VACCINE

Número de solicitud/publicación: 20 22060942
Fecha: 2022-04-25
Solicitante(s): LABORATORIOS HIPRA SA

SARS-COV-2 SUBUNIT VACCINE

Número de solicitud/publicación: 20 22060942
Fecha: 2022-04-25
Solicitante(s): HIPRA SCIENTIFIC SL

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