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SARS-CoV-2: IDT Biologika fills vaccine candidate
Clinical phase about to begin(PresseBox) ( Dessau-Roßlau, )
“We are delighted that we have succeeded in developing a vaccine in such a short time, which is now ready for the clinical test phases,” says CEO Dr. Jürgen Betzing. “Our employees have put in an enormous amount of effort over the past few months to get the development of the vaccine and filling up and running. The path that we are now taking will also aid us in future battles against pandemics. Experience shows that in drastic situations we are capable of responding swiftly in joint interaction with partners and a global network,” emphasizes Dr. Betzing.
In the past months scientists at the German Center for Infection Research (DZIF) and partners IDT Biologika, LMU Munich, Marburg University and the UKE Hamburg have been working flat out to research a new vaccine against SARS-CoV-2. Intensive collaboration and an international network of experts together with the expertise of all partners and experience gained in previous joint projects enabled development to occur in record time and in strict observance of the German health protection requirements of the potential recipients. The aim of the alliance is to make safety and probability of effectiveness the utmost priority. Virologist and Chief Science Officer Dr. Andreas Neubert expects different vaccines to be required for different target groups. The vaccine candidate currently entering the clinical phase is a so-called vector vaccine. For this, genetically-altered and harmless viruses are equipped with genetic information from the coronavirus as carriers. The viruses are not capable of reproducing, but the gene information smuggled in tricks the immune system into identifying an infection and triggering the production of antibodies and a cellular immunity.
The vector vaccine filled at IDT was developed under the leadership of Prof. Gerd Sutter, virologist at LMU Munich, at the DZIF and is based on the “Modified Vaccinia Ankara Virus“ (MVA), which was developed as a vaccine against smallpox over 30 years ago. It has also been used successfully and with very good tolerability in the development of a vaccine against the MERS coronavirus, which occurs on the Arabian peninsula, is transmitted from dromedaries to humans with often fatal consequences and is closely related to SARS-CoV-2.
As with the manufacturing process for the MERS vaccine, which was developed by IDT Biologika, the expertise of the family-run company in Dessau was called for to advance the vaccine candidate from work under laboratory conditions to the prospective production of millions of vaccine doses. Based on nearly 100 years of experience in the development and approval of viral and bacterial vaccines, IDT Biologika developed a cell line and a procedure that enabled the large-scale production of an ultrapure MVA vector vaccine, clearing one of the greatest obstacles in vaccine development. Parallel to this, LMU Munich solved the challenge of producing stable MVA vectors. As all previous experience pointed to extremely good tolerability between the IDT cell technology and the MVA vector of the LMU, the most important prerequisites for a safe and effective vaccine have been met.
Prior to the approval process, the clinical study now aims to demonstrate how effective it actually is, how many vaccinations are required, whether and for how long immunity is triggered and what side-effects may occur. “We have filled the vaccine candidates in low and high concentrations of the active ingredients, so that we can determine the right dosage for the future vaccine,” Dr. Neubert explains. In phase I the vaccine will be tested at UKE Hamburg in a first stage on healthy volunteers aged between 18 and 45, who were selected from thousands of applicants. Whilst the safety of the vaccine is the primary focus of the study, the second phase investigates the dosage, tolerability and effectiveness of the preparation with hundreds of volunteers.
In the coming months IDT Biologika aims to continue working with its partners to swiftly bring the vaccine candidate against SARS-CoV-2 into the next clinical phases.
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