Safety and Immunogenicity of COVI-VAC, a Live Attenuated Vaccine Against COVID-19

COVID-19 Clinical Trial

Official title:

First-in-human, Randomised, Double-blind, Placebo-controlled, Dose-escalation Study in Healthy Young Adults Evaluating the Safety and Immunogenicity of COVI-VAC, a Live Attenuated Vaccine Candidate for Prevention of COVID-19

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04619628
• Other study ID #: CDX-CoV-001
• Status: Completed
• Phase: Phase 1
• Start date: December 11, 2020
• Est. completion date: May 30, 2022

Study information

• Verified date: June 2022
• Source: Codagenix, Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is the first study of COVI-VAC in humans. The purpose of the study is to evaluate the safety and immune response of COVI-VAC (a live attenuated vaccine to prevent COVID-19) in healthy adults aged 18 to 30 years. Approximately 48 participants will be enrolled into 1 of 3 dose groups (low, medium, high). Within each of these dose groups, participants will be assigned randomly to receive either 2 doses of COVI-VAC 28 days apart, 2 doses of placebo (saline), or 1 dose of COVI-VAC and 1 dose of placebo. COVI-VAC or placebo is administered by drops into each nostril. Neither the participants nor the researchers will know whether COVI-VAC or placebo has been received.

To assess the safety of the vaccine, each participant will record symptoms and oral temperature in a diary daily for 14 days after each dose. Safety laboratory tests, physical exams, ECGs, and a chest X-ray will also be performed, and peak expiratory flow and vital signs will be measured. Adverse events and medication use will be recorded.

Blood samples and intranasal samples will be collected to assess the immune response from the vaccine.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: May 30, 2022
• Est. primary completion date: June 26, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 30 Years

Eligibility

Inclusion Criteria:

• Subjects who meet all of the following criteria may be included in the study:

1. Men and women aged between 18 to 30 years of age, inclusive, on the day of signing the informed consent form (ICF)

2. In good health with no history, or current evidence, of clinically significant medical conditions with particular reference to, but not restricted to, hypertension, diabetes, thromboembolic disorders, coronary heart disease, chronic obstructive lung disease, and no clinically significant test abnormalities that will interfere with subject safety, as defined by medical history, physical examination, vital signs (including oxygen saturation), ECG, spirometry, and safety laboratory tests as determined by the Investigator

3. Total body weight of greater or equal to 50 kg and body mass index (BMI) greater or equal to 18.0 kg/m2 and less than or equal to 28.0 kg/m2 (the upper limit of the BMI may be increased to less than or equal to 30 kg/m2 at the Investigator's discretion in case of a muscular healthy subject for whom BMI may be biased upwards)

4. Negative drugs of abuse, cotinine, and alcohol screen (unless explained by prescribed medication)

5. Negative pregnancy test for women who have not been surgically sterilised

6. Negative COVID Clear test

Exclusion Criteria:

Subjects who meet any of the following criteria will be excluded from the study:

1. Haemoglobin A1c =6.0% or 42 mmol/mol

2. Forced expiratory volume in 1 second (FEV1) less than 80% predicted value

3. Signs or symptoms suggestive of upper or lower respiratory tract infection (including fever or persistent cough) within 28 days of Day 1

4. Pregnant, possibly pregnant, or lactating women

5. Women who have been pregnant through the third trimester or given birth within the past 6 months

6. Planning a pregnancy (subject or partner) within 90 days after the last IMP dose

7. Inadequate venous access for repeated phlebotomy

8. History of confirmed or suspected SARS-CoV-2 infection

9. Contact with any individual subsequently confirmed to have SARS-CoV-2 within 14 days after contact

10. History of wheeze treated with inhaler(s)

11. Respiratory symptoms, including wheeze, that have ever resulted in hospitalisation

12. Known bronchial hyperreactivity to viruses

13. Any significant abnormality altering the anatomy of the nose in a substantial way or nasopharynx that may interfere with the aims of the study and in particular any of the nasal assessments or viral challenge (historical nasal polyps can be included, but large nasal polyps causing current and significant symptoms and/or requiring regular treatments in the last month are excluded)

Related Conditions & MeSH terms

• COVID-19

Intervention

Biological:
• COVI-VAC
intranasal, live attenuated vaccine against SARS-CoV-2

Other:
• Placebo
normal saline

Locations

Country	Name	City	State
United Kingdom	hVIVO	London

Sponsors (1)

Lead Sponsor	Collaborator
Codagenix, Inc

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Reactogenicity	Percentage of subjects with reactogenicity events	14 days after each dose
Primary	Adverse events	Percentage of subjects with adverse events	Days 1 through 57
Primary	Serious adverse events	Percentage of subjects with serious adverse events	Days 1-400
Secondary	IgG titre	IgG titre measured by ELISA in serum collected on Days 1, 15, 29, 43, 57, 120, 210, and 400	Days 1, 15, 29, 43, 57, 120, 210, and 400
Secondary	Neutralizing antibody titre	Neutralising antibody level measured by microneutralisation assay in serum	Days 1, 15, 29, 43, 57, 120, 210, and 400