Safety Study of Live Attenuated Influenza Vaccine, CodaVax

Codagenix

Status and phase

Completed

Phase 1

Conditions

Influenza

Treatments

Biological: Fluzone quadrivalent

Biological: CodaVax-H1N1

Study type

Interventional

Funder types

Industry

Identifiers

NCT03926416

CODA01-001

Details and patient eligibility

About

This study is being conducted to assess the safety, tolerability, and immunogenicity of the CodaVax-H1N1 influenza vaccine as compared to active and placebo controls when administered to healthy adults.

Full description

This randomized, double-blind, placebo and active controlled Phase I study is intended to study the effects of a live-attenuated vaccine against influenza A H1N1. Part 1 of this study will enroll 75 participants at a single site. Participants will be randomized in a 2:2:1 ratio to receive one dose each of either CodaVax-H1N1, FluZone quadrivalent, or placebo. This study is conducted during the influenza "off season" in Australia. Part 2 of the study will enroll an 50 additional participants randomized to receive either CodaVax-H1N1 at a higher dose or placebo (40:10).

Enrollment

125 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

In good health, in the opinion of the Medical Investigator (with or without the Sponsor), with no significant medical history and no clinically significant abnormal findings at screening. Particular attention will be paid to:
- A drug history identifying any known drug allergies and the presence of drug abuse;
- Any chronic use of medication(s); and
- Thorough review of body systems
Women of child bearing potential (WOCBP) must use highly effective, double contraception from the Screening Visit and up to the Follow-up visit (Day 30 ± 2 days). Double contraception is defined as a condom AND one other form of the following:
- Established hormonal contraception (with approved oral, injected or depot regimen) for at least 2 months prior to screening
- Depot or injectable birth control
- Intrauterine device or intrauterine system in place for at least 2 months prior to screening
- Documented evidence of surgical sterilization at least 6 months prior to screening visit. i.e., tubal ligation or hysterectomy for women or vasectomy for men (with appropriate post-vasectomy documentation of the absence of sperm in semen) provided the male partner is a sole partner; Males must not donate sperm for at least 70 days post-dose of the last study treatment. Male partners of female participants and female partners of male participants must also use contraception, if they are of childbearing potential.

Women of childbearing potential must have a negative serum pregnancy test at Screening and Day 30. Women not of childbearing potential must be postmenopausal (defined as cessation of regular menstrual periods for at least 12 months), confirmed by FSH level meets the requirement of post-menopausal women if in doubt. Periodic abstinence (e.g. calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not considered highly effective methods of birth control. Participant abstinence for the duration of the study and 1 month after the last study treatment is acceptable.

Must be willing to comply with the following conditions to prevent the spread of GMOs according the OGTR Licence (DIR 144):
1. Hygiene measures intended to prevent interpersonal transmission of study drug must be implemented, including but not limited to frequent handwashing with soap or hand disinfectant, respiratory hygiene and cough etiquette within 7 days following vaccination
2. Blood, tissue or organs must not be donated within 7 days of vaccination
3. Severely immunosuppressed persons who require a protective environment are not to be cared for by the participant within 7 days of vaccination
4. Contact is not to be made with severely immunosuppressed persons who require a protective environment within 7 days of vaccination
5. All tissues and materials used to collect respiratory secretions are to be sealed in a primary container and placed within a secondary container so that it is not accessible to children or animals for 7 days until it is returned to the study site for disposal, for 7 days within vaccination
Adequate venous access in the left or right arms to allow collection of a number of blood samples
No birthmarks, tattoos, wounds or other skin conditions which could reasonably obscure IM injection site reactions
Able to communicate effectively with study personnel and considered reliable, willing and cooperative in terms of compliance with the protocol requirements
Participant does not intend to start or change an existing physical conditioning regimen prior to or during the study period
Participant has voluntarily given written informed consent to participate in the study (prior study entry)
Participant is available for the duration of the study

Exclusion criteria

Immunodeficiency (including HIV) or autoimmune disorder, or participant is currently taking drugs or was undergoing a form of treatment within 6 weeks prior to study entry that affects the immune system. (Treatment of asthma with low dose corticosteroids equivalent to prednisone <10 mg/day, is permitted).
Participant is not to have had Guillain-Barre Syndrome
Received blood or blood products in the 3 months prior to screening
Received another vaccine within 30 days before screening
Received another influenza vaccine within 2 years prior to screening
Participated in another clinical study (involving an investigational product or device) within 60 days before screening (including studies for FluMist®)
Suffered previous anaphylactic reaction to foods, vaccines, drugs or hymenoptera stings, or has a history of severe allergic reactions (e.g. clinically severe urticaria, asthma)
Participants with active asthma currently managed by ad lib with inhalers
Participants with a known egg allergy
If female, pregnant, planning to become pregnant, or lactating
Participant has a history of, or current evidence at the time of screening of abuse of alcohol or any drug substance, licit or illicit, or current alcohol consumption is > 4 standard drinks (or equivalent) per day
History of any psychiatric illness or psychological disorder which may impair the ability to provide written informed consent or participate in the study
Current or history of significant neurological, cardiovascular, pulmonary (including asthma), hepatic, rheumatic, autoimmune, haematological, metabolic or renal disorder
Clinically significant abnormal laboratory value at screening as determined by the Investigator
Unusual dietary habits and excessive or unusual vitamin intake likely, in the opinion of the Investigator, to affect safety pathology parameters
Participant is seropositive to Human Immunodeficiency Virus (HIV-1 or HIV-2), Hepatitis C Virus (HCV) or HBV.
Body temperature (oral) ≥38.0ºC or acute illness within 5 days prior to vaccination
Any skin marking, tattoo or blemish precluding injection site inspection.
Any other significant finding that, in the opinion of the Investigator, would increase the risk of the individual having an adverse outcome from participating in this study
Participant is a member of the team or is related or in a dependent relationship with a member of the study team, as defined as the Sponsor or study site personnel

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

125 participants in 4 patient groups, including a placebo group

CodaVax-H1N1, low dose

Experimental group

Description:

Participants will receive a single dose of either CodaVax (5 x 10\^3 PFU in 200 uL) and an intramuscular injection of placebo

Treatment:

Biological: CodaVax-H1N1

Fluzone

Active Comparator group

Description:

Participants will receive an intranasal (IN) dose of placebo and an intramuscular (IM) dose of QuadriFlu- Tetravalent Influenza Vaccine (TIV) (Fluzone®)

Treatment:

Biological: Fluzone quadrivalent

CodaVax-H1N1, high dose

Experimental group

Description:

Participants will receive a single intranasal (IN) dose of CodaVax-H1N1 (1 x 10\^5 PFU in 500 uL)

Treatment:

Biological: CodaVax-H1N1

Placebo

Placebo Comparator group

Description:

Leibovitz's L-15 medium (IN) or saline (IM)