Intramuscular CodaVax-H1N1 in Healthy Adults

Influenza, Human Clinical Trial

Official title:

Randomised, Double-blind, Placebo-controlled, Dose-escalation Study of the Safety, Tolerability, and Immunogenicity of Intramuscular CodaVax-H1N1 in Healthy Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05223179
• Other study ID #: CDX-FLU-103
• Status: Completed
• Phase: Phase 1
• Start date: April 11, 2022
• Est. completion date: February 9, 2024

Study information

• Verified date: May 2024
• Source: Codagenix, Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a Phase 1, 2-part, randomised, double-blind, controlled, clinical trial to evaluate the safety and immune response of CodaVax-H1N1 in healthy adults aged 18 to 49 years. Participants will be enrolled in autumn 2022 (southern hemisphere) and followed through the 2022 influenza season (Part A) or enrolled in autumn 2023 and followed through the 2023 influenza season (Part B). Participants will be screened within 28 days of randomization, and eligible participants in Part A will be enrolled into 1 of 3 sequential cohorts and randomised to receive a single dose of CodaVax-H1N1, placebo (normal saline), or licenced injectable seasonal influenza vaccine (Flucelvax Quad). Each subsequent cohort will include a higher dose of CodaVax H1N1 than the previous cohort, in addition to placebo and the licensed injectable seasonal influenza vaccine. In Part B, 24 eligible participants will be enrolled into 1 of 2 sequential cohorts and randomised to receive a single IM dose of CodaVax-H1N1 or placebo.

Description:

This study is a Phase 1, 2-part, randomised, double-blind, controlled, clinical trial to evaluate the safety and immune response of CodaVax-H1N1 in healthy adults aged 18 to 49 years. Participants will be enrolled in autumn 2022 (southern hemisphere) and followed through the 2022 influenza season (Part A) or enrolled in autumn 2023 and followed through the 2023 influenza season. Participants will be screened within 28 days of randomization, and eligible participants in Part A will be enrolled into 1 of 3 sequential cohorts and randomised to receive a single dose of CodaVax-H1N1, placebo (normal saline), or licensed injectable seasonal influenza vaccine (Flucelvax Quad). Each subsequent cohort will include a higher dose of CodaVax H1N1 than the previous cohort, in addition to placebo and the licensed injectable seasonal influenza vaccine. In Part B, 24 eligible participants will be enrolled into 1 of 2 additional sequential cohorts and randomised to receive a single IM dose of CodaVax-H1N1 or placebo.

Participants will record reactogenicity events (local events, systemic events, and temperature) in a daily diary for 7 days after the dose. Each participant will be contacted by telephone on the day after dosing for safety assessment and review of the diary data. Participants will return to the clinic on Days 4, 8, 29, 91, and 181 for safety and immune response assessments.

All adverse events and concomitant medications will be recorded from signing of the informed consent form (ICF) to 28 days postdose. After 28 days until the end of the study, only medically attended adverse events (MAAEs), new onset chronic illnesses (NCIs), serious adverse events (SAEs), immunosuppressive medications, blood products like transfusions or infusions, and vaccines will be recorded. A complete physical examination will be performed at Screening, and targeted and symptom-driven physical examinations will be performed predose on Day 1, 2 hours postdose, and at each postdose visit through Day 91. Vital signs will be measured at the same time points. An electrocardiogram (ECG) will be performed at Screening and on Day 29.

A serum sample will be collected predose and on Days 29, 91, and 181 for measurement of immune response.

A whole blood sample will be collected predose and on Day 8 and PBMCs isolated for measurement of T-cell response.

If a participant experiences acute symptoms compatible with viral respiratory infection, nasopharyngeal swab samples will be collected for a rapid influenza diagnostic test and respiratory virus PCR assay panel (including SARS-CoV-2) as indicated for symptomatic respiratory infection and will perform the rapid influenza diagnostic test.

The primary analysis of study data will be conducted after all participants complete the Day 29 visit. The final analysis will be conducted at the end of the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 69
• Est. completion date: February 9, 2024
• Est. primary completion date: February 9, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 49 Years

Eligibility

Inclusion Criteria:

• Body mass index (BMI) = 18 and = 35 kg/m2

• In good health with no history, or current evidence, of clinically significant medical conditions

• Negative SARS-CoV-2 test predose on Day 1

• For all women, negative pregnancy test

• Agreement to comply with conditions to prevent the spread of genetically modified organisms (GMOs)

Exclusion Criteria:

• Pregnant or lactating women or women who plan to become pregnant through Day 29

• Inadequate venous access for repeated phlebotomy

• History of severe reaction to vaccination

• Receipt of any licenced or investigational influenza vaccine within 6 months before Day 1

• Receipt of any live vaccine within 30 days before Day 1

• Tattoo, skin reaction, or other condition at the injection site that would interfere with assessment of local reactogenicity

Related Conditions & MeSH terms

• Influenza, Human

Intervention

Biological:
• CODA-VAX H1N1
Intramuscular Live Attenuated Influenza H1N1 Vaccine
• Flucelvax Quad
Licensed Seasonal Injectable Influenza Vaccine

Other:
• Saline
Saline

Locations

Country	Name	City	State
Australia	Lis Gilmour, Senior Project Manager	Morayfield	Queensland

Sponsors (1)

Lead Sponsor	Collaborator
Codagenix, Inc

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and Tolerability by Assessing Percentage of Participants with Reactogenicity Events	Percentage of participants with reactogenicity events	Reactogenicity events from Day 1 to Day 7
Primary	Safety and Tolerability by Assessing Percentage of Participants with Adverse Events	Percentage of participants with adverse events	Adverse events (AEs) from Day 1 to Day 29
Primary	Safety and Tolerability by Assessing Percentage of Participants with MAAEs, NCIs, and SAEs.	Percentage of participants with MAAEs, NCIs, and SAEs.	MAAEs, NCIs, SAEs from Day 1 to Day 181
Secondary	Humoral Immunogenicity	To assess the humoral immunogenicity elicited by CodaVax-H1N1 at nominal doses of 5×104, 5×105, and 5×106 PFU by IM injection	HAI assay titre against A/California/07/2009 and the current seasonal influenza vaccine H1N1 and H3N2 strains measured in samples collected on Days 1, 29, 91, and 181