Phase Ia, open-label, escalating dose study to evaluate the safety and immunogenicity of therapeutic vaccine, TherVacB.
Following 12 years of research, the first-in-human clinical trial of TherVacB, a therapeutic vaccine for the treatment of hepatitis B, was initiated on January 25, 2024, according to a press release.1
The trial is a Phase Ia, open-label, escalating dose study to evaluate the safety and immunogenicity of TherVacB in 24 healthy participants aged 18 to 65 years. Under the sponsorship of the University Medical Center Hamburg-Eppendorf, the Division of Infectious Diseases and Tropical Medicine at the LMU University Hospital Munich is responsible for conducting the clinical trial.
According to the World Health Organization, hepatitis B affects approximately 296 million people globally, including over 6 million children under the age of 5.2
“TherVacB is based on a deep understanding of the challenges of the immune system in chronic hepatitis B infection and is the result of years of dedicated research here in Munich,” said Ulrike Protzer, the leading scientist behind the vaccine in the press release. “Our approach is designed to induce exactly the type of immunity required and cover a broad spectrum of over 95% of hepatitis B strains worldwide.”
While the Phase Ia study is underway, preparations have begun for applying for the first-in-patient Phase Ib/IIa trial, aiming to assess the safety and efficacy of TherVacB in patients with chronic hepatitis B. This study is planned to take place in Germany, Italy, Spain, England, and Tanzania and is funded by the European Union as part of a Horizon 2020 research project.
According to the press release, researchers have found that the hepatitis B virus prevents certain immune cells of the body from becoming effective. Over the past two decades, attempts at developing an effective therapy for hepatitis B have been unsuccessful. In response, scientists at Helmholtz Munich, in collaboration with the German Center for Infection Research and the Proof-of-Concept Initiative of the Helmholtz Association and the Fraunhofer-Gesellschaft, have developed a novel therapeutic approach to activate these immune cells by therapeutic vaccination to cure chronic hepatitis B infection with TherVacB.
Results from the Phase Ia study (NCT05727267) of TherVacB are expected to be made public by the end of 2024.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.