A Study to Assess New Ebola Vaccines, cAd3-EBO Z and MVA-BN® Filo

Ebola Clinical Trial

Official title:

A Phase Ia, Dose-Escalating, Safety and Immunogenicity Trial of the Monovalent Zaire Ebola Viral Vector Candidate Vaccine cAd3-EBO Z and the Heterologous Prime-boost Candidate Vaccine Regimen cAd3-EBO Z and MVA-BN® Filo in Healthy UK Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02240875
• Other study ID #: EBL01
• Secondary ID: 2014-003518-10
• Status: Completed
• Phase: Phase 1
• Start date: September 17, 2014
• Est. completion date: August 22, 2017

Study information

• Verified date: July 2018
• Source: University of Oxford
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess two new Ebola vaccines: cAd3-EBO Z at 3 different doses, and a second vaccine, MVA-BN® Filo, at 3 different doses. The study will enable us to assess the safety of the vaccines and the extent of the immune response in healthy volunteers. The investigators will do this by giving volunteers a either one or two vaccinations, doing blood and saliva tests and collecting information about any symptoms that occur after vaccination. This is the first trial to use either of these vaccines in humans. We plan to recruit a total of 92 volunteers to be vaccinated.

Description:

Long- term immunology follow-up: In order to assess the durability of vaccine induced immunogenicity, all vaccinated subjects will be invited back to attend a maximum of 3 further optional follow up visits at least 12 months after their final vaccination. The 3 visits will have a minimum interval of 3 months between them, and the final visit must take place no longer than 12 months after the first optional visit.

Volunteers who attend these visits will be asked about occurrence of any SAEs during the intervening period. SAE data for this period will not be collected in those volunteers who decline to attend these additional visits.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 91
• Est. completion date: August 22, 2017
• Est. primary completion date: August 22, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Healthy adults aged 18 to 50 years

• Able and willing (in the Investigator's opinion) to comply with all study requirements

• Willing to allow the investigators to discuss the volunteer's medical history with their general practitioner (GP)

• For females only, willingness to practice continuous effective contraception during the study and a negative pregnancy test on the day(s) of screening and vaccination

• Agreement to refrain from blood donation during the course of the study

• Provide written informed consent

Exclusion Criteria:

• Participation in another research study involving receipt of an investigational product in the 30 days preceding enrolment, or planned use during the study period

• Prior receipt of an investigational Ebola or Marburg vaccine, a chimpanzee adenovirus vectored vaccine or any other investigational vaccine likely to impact on interpretation of the trial data

• Receipt of any live, attenuated vaccine within 28 days prior to enrolment

• Receipt of any subunit or killed vaccine within 14 days prior to enrolment

• Administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate

• Any confirmed or suspected immunosuppressive or immunodeficient state, including HIV infection; asplenia; recurrent, severe infections and chronic (more than 14 days) immunosuppressant medication within the past 6 months (inhaled and topical steroids are allowed)

• History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, (e.g. egg products) including urticaria, respiratory difficulty or abdominal pain

• Any history of hereditary angioedema, acquired angioedema, or idiopathic angioedema.

• Any history of anaphylaxis in reaction to vaccination

• Pregnancy, lactation or willingness/intention to become pregnant during the study

• History of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ)

• History of serious psychiatric condition

• Poorly controlled asthma or thyroid disease

• Seizure in the past 3 years or treatment for seizure disorder in the past 3 years

• Bleeding disorder (eg. Factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following intramuscular injections or venepuncture

• Any other serious chronic illness requiring hospital specialist supervision

• Current anti-tuberculosis prophylaxis or therapy

• Suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week

• Suspected or known injecting drug abuse in the 5 years preceding enrolment

• Seropositive for hepatitis B surface antigen (HBsAg)

• Seropositive for hepatitis C virus (antibodies to HCV)

• Travel to a Ebola or Marburg endemic region during the study period or within the previous six months

• Any clinically significant abnormal finding on screening biochemistry or haematology blood tests or urinalysis (see Appendix A and Appendix B)

• Any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data

• Inability of the study team to contact the volunteer's GP to confirm medical history and safety to participate

Related Conditions & MeSH terms

• Ebola
• Ebola Zaire
• Hemorrhagic Fever, Ebola

Intervention

Biological:
• cAd3-EBO Z at 1 x 10^10 vp
Low dose cAd3-EBO Z
• cAd3-EBO Z at 2.5 x 10^10 vp
Medium dose cAd3-EBO Z
• cAd3-EBO Z at 5 x 10^10 vp
High dose cAd3-EBO Z
• 4.4x10^8 TCID50s MVA-BN® Filo
High dose MVA-BN® Filo
• 2.2x10^8 TCID50s MVA-BN® Filo
Low dose MVA-BN® Filo
• 4.4 x 10^7 TCID50s MVA-BN® Filo
Very low dose MVA-BN® Filo

Locations

Country	Name	City	State
United Kingdom	Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford	Oxford	Oxfordshire

Sponsors (3)

Lead Sponsor	Collaborator
University of Oxford	National Institute of Allergy and Infectious Diseases (NIAID), Wellcome Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and tolerability of the Ebola Zaire vaccine cAd3-EBO Z when administered to healthy volunteers at 3 doses	The specific endpoints for safety and reactogenicity will be actively and passively collected data on adverse events.	6 months
Secondary	Cellular and humoral immunogenicity of the Ebola Zaire vaccine cAd3-EBO Z when administered to healthy volunteers at 3 doses	The primary immunogenicity outcome measures are ELISA and neutralization antigen-specific assays for antibody responses and intracellular cytokine staining (ICS) assay for T cell responses.	6 months