Safety and Immunogenicity of the Candidate Rabies Vaccine ChAdOx2 RabG

Rabies Clinical Trial

Official title:

A Phase I Clinical Trial to Determine the Safety and Immunogenicity of the Candidate Rabies Vaccine ChAdOx2 RabG in UK Healthy Adult Volunteer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04162600
• Other study ID #: RAB001
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: January 2, 2020
• Est. completion date: September 2023

Study information

• Verified date: May 2022
• Source: University of Oxford
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a first-in-human, open-label, dose escalation, phase I clinical trial to assess the safety and immunogenicity of the candidate ChAdOx2 RabG vaccine in healthy UK volunteers aged 18-65. The vaccine will be administered intramuscularly (IM).

Description:

Volunteers will be recruited and vaccinated at the Centre for Clinical Vaccinology and Tropical Medicine (CCVTM), Oxford. There will be 3 study groups and it is anticipated that a total of 12 volunteers will be enrolled. Staggered enrolment will apply between study groups and for the first three volunteers within each group. The study includes an optional extended follow-up period, lasting one month and starting one year after vaccination. Volunteers will receive a complete pre-exposure prophylactic course of an existing rabies vaccine, allowing study of the immunological memory (recall response) induced by ChAdOx2 RabG. A second optional element of the study is the collection of saliva samples at each visit for the study of shedding of EBV and CMV.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 18
• Est. completion date: September 2023
• Est. primary completion date: September 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Healthy adults aged 18 to 65 years.

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

3. Willing to allow the investigators to discuss the volunteer's medical history with their GP.

4. 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(s).

5. Agreement to refrain from blood donation during the course of the study.

6. Provide written informed consent.

Exclusion Criteria:

1. Participation in another research study involving receipt of an investigational product in the 30 days preceding enrolment, or planned use during the study period. To be re- confirmed at the enrolment visit.

2. Prior receipt of an investigational vaccine likely to impact on interpretation of the trial data (e.g. Adenovirus vectored vaccine).

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

4. 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).

5. History of allergic disease or reactions likely to be exacerbated by any component of the vaccine.

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

7. Any history of anaphylaxis in relation to vaccination.

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

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

10. History of serious psychiatric condition likely to affect participation in the study.

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

13. Individuals who have previously experienced episodes of capillary leak syndrome.

14. History of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism).

15. History of antiphospholipid syndrome. 16. History of prior receipt of unfractionated heparin. 17. History of heparin induced thrombocytopenia. 18. Any other serious chronic illness requiring hospital specialist supervision.

19. Suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. 20. Suspected or known injecting drug abuse in the 5 years preceding enrolment. 21. Detectable circulating hepatitis B surface antigen (HBsAg). 22. Seropositive for hepatitis C virus (antibodies to HCV). 23. Any clinically significant abnormal finding on screening biochemistry or haematology blood tests or urinalysis. 24. 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.

25. Inability of the study team to contact the volunteer's GP to confirm medical history and safety to participate. 26. Receipt of any prior rabies vaccine, including an incomplete course. 27. Require or will require rabies vaccination during the first 8 weeks of the study period (e.g. through planned travel to high risk enzootic areas of through work which may lead to exposure and for which rabies vaccination is usually required/recommended). Exclusion criteria for optional follow-up

1. Receiving rabies vaccination following the completion of the first 8 weeks of follow-up but before the optional extended follow-up period will exclude participants from taking part in the optional follow-up period.

2. History of allergic reactions to amphotericin B, chlortetracycline, neomycin, polymyxin, streptomycin, or to any antibiotics of the same groups will exclude participants from receiving certain IRVs (as per the relevant SmPC) during the optional extended follow-up period, but will not exclude participants from receiving ChAdOx2 RabG.

Related Conditions & MeSH terms

• Rabies

Intervention

Biological:
• ChAdOx2 RabG
Single dose of ChAdOx2 RabG at different concentrations: 5 x 10^9 vp, 2.5 x 10^10 vp, 5 x 10^10 vp
• Inactivated Rabies Vaccine
A complete pre-exposure prophylactic course of an existing rabies vaccine, =2.5 international units

Locations

Country	Name	City	State
United Kingdom	CCVTM, University of Oxford, Churchill Hospital	Oxford

Sponsors (1)

Lead Sponsor	Collaborator
University of Oxford

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Immunological memory induced by ChAdOx2 RabG	Virus neutralizing antibody will be measured before and in the course of immunisation with IRVs during an optional extended follow-up.	Between days 365 and 386
Other	Timecourse of EBV and CMV shedding	Measured by quantitative PCR.	Study Duration (386 days)
Other	Level of EBV and CMV shedding	Measured by quantitative PCR.	Study Duration (386 days)
Primary	Safety and tolerability of ChAdOx2 RabG in healthy volunteers given as a standalone vaccine at different doses assessed by the occurrence of solicited adverse events.	Occurrence of solicited local and systemic adverse events (i.e: pain, redness, swelling and pruritus at injection site and temperature, feverishness, myalgia, arthralgia, malaise, headache, fatigue and nausea).	Assessment of solicited AEs in the first 7 days post vaccination
Primary	Safety and tolerability of ChAdOx2 RabG in healthy volunteers given as a standalone vaccine at different doses assessed by the occurrence of solicited adverse events.	Occurrence of unsolicited local and systemic adverse events	Unsolicited AEs to be assessed up to 28 days post vaccination.
Primary	Safety and tolerability of ChAdOx2 RabG in healthy volunteers given as a standalone vaccine at different doses assessed by the occurrence of serious adverse events.	Occurrence of serious adverse events	SAEs will be collected from enrolment until the end of the follow-up period.(8 weeks)
Primary	Safety and tolerability of ChAdOx2 RabG in healthy volunteers given as a standalone vaccine at different doses assessed by the occurrence of solicited adverse events.	Occurrence of laboratory adverse events defined as clinically significant changes from baseline. Haematology (Full Blood Count) and Biochemistry (Kidney and Liver Function Tests) will be assessed.	At Day 0 (baseline), day 2, day 7, day 28 and day 56 post vaccination
Secondary	Immunogenicity of the ChAdOx2 RabG vaccine	Rapid fluorescent focus inhibition test (RFFIT) of virus neutralising antibody	Day 365