In this phase I first-in-human clinical trial, healthy volunteers in two different dose cohorts will be vaccinated twice with the candidate vaccine MVA-SARS-2-S. A subgroup will receive a heterologous booster vaccination with a licensed COVID-19 vaccine. The aim of the study is to assess the safety and tolerability of the candidate vaccine and to characterize its immunogenicity.
The vaccine contains a Modified Vaccinia Virus Ankara (MVA) vector expressing the SARS-CoV-2
spike protein (S). A total of 30 participants will receive the following vaccine regime:
15 participants will receive 10^7 infectious units (IU) of MVA-SARS-2-S on days 0 and 28.
15 participants will receive 10^8 IU of MVA-SARS-2-S on days 0 and 28. Safety and
immunogenicity data will be collected throughout the study, which concludes at day 168.
A subgroup will receive a heterologous booster vaccination with a licensed COVID-19 vaccine.
Vaccinees will receive two doses of the Comirnaty vaccine (21 days interval).
Biological: MVA-SARS-2-S vaccinations (days 0 & 28)
Vaccination with MVA-SARS-2-S in two escalating dose regimens
Biological: Comirnaty
Vaccination with Comirnaty (21 day interval)
Inclusion Criteria:
- Written informed consent
- Healthy male and female adults aged 18-55 years
- No clinically significant health problems as determined during medical history and
physical examination at screening visit
- Body mass index 18.5 - 30.0 kg/m2 and weight > 50 kg at screening
- Adults male or non-pregnant, non-lactating female with negative pregnancy test
- Males and females who agree to comply with the applicable contraceptive requirements
of the protocol
Inclusion criteria for the subjects before the 3rd/4th (=booster) vaccination:
1. Ability to understand the subject information and to personally name, sign and date
the in-formed consent to participate in the study.
2. Provided written informed consent.
3. Continues to be in stable health condition as determined during medical history and
physi-cal examination on vaccination visits.
4. Non-pregnant, non-lactating female with a negative pregnancy test at screening and on
dosing days (prior to vaccination).
5. Be willing to refrain from blood donation during the course of the study.
6. The subject is co-operative and available for the entire study.
7. Need to have participated in previous part of the MVA-SARS-2-S vaccine study (Eudra-CT
No: 2020-002998-10)
Exclusion Criteria:
- Prior exposure to SARS-CoV-2
- Receipt of any vaccine from 4 weeks prior to each trial vaccination (8 weeks for live
vaccines) to 6 weeks after each trial vaccination
- Previous rMVA immunization
- Known allergy to the components of the SARS-CoV-2 vaccine product
- Known history of anaphylaxis to vaccination or any allergy likely to be exacerbated by
any component of the trial vaccine
- Evidence in the subject's medical history or in the medical examination that might
influence either the safety of the subject or the absorption, distribution, metabolism
or excretion of the investigational product
- Clinically relevant findings in ECG
- Any confirmed or suspected immunosuppressive or immunodeficient condition, cytotoxic
therapy in the previous 5 years, and/or diabetes
- Any chronic or active neurologic disorder, including seizures, and epilepsy, excluding
a single febrile seizure as a child
Exclusion criteria for the subjects before the 3rd/4th (=booster) vaccination:
1. Prior infection with SARS-CoV-2 in medical history (documented by PCR test)
2. Receipt of any vaccine from 2 weeks prior to each trial vaccination (4 weeks for live
vac-cines) to 2 weeks after each trial vaccination.
3. Receipt any COVID-19 vaccine (investigational or licensed other than MVA-SARS-2-S
be-fore vaccination throughout end of study).
4. Known allergy to the components of t Comirnaty®.
5. Known history of anaphylaxis to vaccination or any allergy likely to be exacerbated by
any component of the trial vaccine.
6. Participation in a clinical trial other than the MVA-SARS-2-S vaccine trial or use of
an in-vestigational product other than MVA-SARS-2-S within 30 days or five times the
half-life of the investigational product -whichever is longer- prior to receiving the
first dose within this study.
7. Evidence in the subject's medical history or in the medical examination that might
influence
CTC North GmbH & Co KG at the University Medical Center Hamburg-Eppendorf
Hamburg, Germany
Marylyn M Addo, MD, Principal Investigator
Universitätsklinikum Hamburg-Eppendorf