TherVacB - A therapeutic vaccine against hepatitis B

Copyright: The scientific staff License: Creative Commons Attribution (CC-BY)

The role of viral hepatitis as a public health threat has long been underestimated. Hepatitis B virus (HBV) alone, which causes liver cirrhosis and liver cancer, kills 880,000 people worldwide each year as a result of infection. A prophylactic vaccine is available to prevent HBV infection, but more than 3% of the world's population (approximately 260 million people) are chronically infected and can no longer benefit from this vaccine. For people suffering from chronic hepatitis B, there is still no cure.

The consortium of Helmholtz Zentrum München - German Research Center for Environmental Health (HMGU), Fraunhofer Institute for Cell Therapy and Immunology (IZI), University Medical Center Hamburg Eppendorf (UKE), Klinikum rechts der Isar (MRI) of Technische Universität München (TUM) and Hochschulmedizin MRI (TUM), aims to conduct a first-in-human clinical phase 1a study to demonstrate the safety and immunogenicity of a novel therapeutic agent against chronic hepatitis B. This therapeutic vaccine was developed at the Institute of Virology (HMGU).

Furthermore, a patient:inside register is to be established for further studies.

 

Here you can find the link to the Website of the TherVacB project

The project team can be reached via the Website contact form

 

The consortium is also running an awareness campaign. Here you can find the Information flyer (PDF)

 

The consortium tweets at @TherVacB_EU

 

Are you a hepatitis B patient and interested in the study? Here you will find more information and contacts.

Partner

  • Helmholtz Zentrum München - German Research Center for Environmental Health (HMGU)
  • Fraunhofer Institute for Cell Therapy and Immunology (IZI)
  • University Medical Center Hamburg Eppendorf (UKE) and
  • Klinikum rechts der Isar (MRI) of the Technical University of Munich (TUM)
  • University Medicine MRI (TUM)

Subproject

Ethics Subproject:

The research group of Prof. Alena Buyx at the Institute for History and Ethics of Medicine at the Technical University of Munich is in charge of the following work package within this consortium "Ethics of Patient Recruitment.. We are investigating the ethical-social implications related to patient recruitment via social media (e.g. Facebook, Twitter) and are advising the consortium on the development of a recruitment strategy via social media.

Recruitment via social media for clinical trials promises to be a cost-effective method of targeting traditionally marginalized populations and promoting patient engagement with researchers and a particular study. Although social media recruitment has been shown to have significant potential, it comes with several practical, ethical, social, and legal challenges. These range from inadvertent unblinding, misinformation, and limited participant autonomy to issues of inequitable access and the digital divide and potentially stigmatizing effects, to name a few. In addition, there are significant uncertainties regarding legal issues in social media recruitment, as well as privacy and data security, including in light of the EU General Data Protection Regulation. Recruitment via social media for clinical trials therefore requires a precise and context-based ethical analysis to also consider the risks of this approach.

The TherVacB consortium, whose TherVacB clinical trial is a potential use case for social media recruitment, is exploring the application of the new approach. To this end, our research team is developing an overview of the ethical benefits and risks to be considered when recruiting via social media in clinical trials, and developing practical recommendations for how these considerations can be implemented in the TherVacB setting. In addition, the metrics and checklists developed can serve as a blueprint for other clinical researcher:s considering social media recruitment for their trials. In this way, we hope to minimize the risks associated with social media recruitment for patients and subjects not only for the TherVacB clinical trial, but for all clinical trials.

To support the recommendations, in addition to an extensive ongoing literature review, our team conducted a multi-stakeholder interview study with (1) patients who use social media and/or have been exposed to social media recruitment, (2) social media researchers:(1) social media researchers or social scientists who have worked with social media (recruitment), (3) practical experts in SMR, (4) legal experts, (5) members of ethics committees (DACH), (6) members of ethics committees (USA), and (7) members of the TherVacB consortium. The study was approved by the Ethics Committee of the Technical University of Munich, Klinikum Rechts der Isar.

Based on the interview study, our research team is developing a survey study to quantify the results. The primary objective of the survey study is to investigate the acceptance of social media as a recruitment channel for clinical trials in a vulnerable patient population (hepatitis B patients). In addition, factors influencing this acceptance that could be identified from the previous interview study will be quantified.

Theresa Willem
Tel.: +49 89 4140 4042
Mail: theresa.willem@tum.de
Ismaninger Street 22, 81675 Munich

Project Management:
Prof. Dr. med. Alena Buyx

Period:
January 2020 until December 2024

Project Type:
EU consortium

Funding source:
European Union's Horizon 2020 research and innovation program

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