A Clinical Trial to Study the COVAC-1 Booster Dose in Generally Healthy Adults

University of Saskatchewan

Status and phase: Completed; Phase 1

Conditions: Severe Acute Respiratory Syndrome Coronavirus 2 Infection

Treatments: Biological: COVAC-1; Biological: Saline Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT05693272

COVAC-005

Details and patient eligibility

About

VIDO has developed a vaccine called COVAC-1.

The COVAC-1 study vaccine contains a portion of the SARS-CoV-2 spike protein, called S1. The spike protein is the part of the virus that is responsible for attaching to the surface of host cells. COVAC-1 contains a TriAdj adjuvant. An adjuvant is a compound that is added to a vaccine to help the vaccine produce a better immune response. The vaccine is expected to stimulate the body to make antibodies against the S1 protein. The antibodies will recognize the viral spike protein if the body is exposed to the virus and prevent COVID-19 illness. In animal studies, the immune response generated by the COVAC-1 vaccine was able to protect the vaccinated animals against a severe SARS-CoV-2 infection.

The COVAC-005 Study is a Phase I, multi-centre trial of a SARS-CoV-2 vaccine booster. This is a randomized, observer-blinded, and placebo-controlled study to assess the safety and immunogenicity of COVAC-1 booster dose administered once in generally healthy adults 18-65 years of age who have received a minimum of 2 doses of an authorized COVID-19 vaccine at least 4 months prior to Day 0.

The study will follow a dose-escalation design to test the safety and immunogenicity of three dosage levels (10, 25 and 50 µg). In each dose escalation group participants will be randomized in a 3:1 ratio, to receive either the investigational product or a placebo, respectively. Stratification will be according to the Investigational product dose received. Sub-analysis will be completed in two age groups, 18-54 and 55-65 years.

Study participants will be initially randomized to the lowest dose of 10 µg or placebo. After approval by the Sponsor and based on the recommendations from the DSMB following the Day 7 safety analysis, new study participants will be allowed to be randomized in the higher dose escalation group of 25 µg. Approval will also be sought from the Sponsor, based upon the DSMB recommendation, to proceed with the higher dose of 50 µg. Within each dose escalation group of 16 participants (12 active vaccine recipients, and 4 placebo recipients) it is proposed to randomize a first cohort of 4 participants, including at least 3 active vaccine recipients, and pending no holding rule is met after 48 hours, as determined by the post-injection phone call, the remaining 12 participants within that dose escalation group will be randomized.

Enrollment: 47 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Male and female participants 18-65 years of age at the time of signing the informed consent form for the study.
2. Good general health as confirmed by assessments completed no more than 30 days before study D0. Participants with mild to moderate well controlled comorbidities or having a medically stable condition, will be eligible. A stable medical condition is defined as disease not requiring significant change in therapy or hospitalization due to worsening during the 3 months prior to enrollment, and according to the judgment of the Investigator, hospitalization during the entire study period is not anticipated.
3. Have received a minimum of 2 doses of an authorized COVID-19 vaccine at least 4 months prior to the investigational booster dose injection. Proof of vaccination can be provided as a digital copy of the vaccination receipt on the participant's device, a screenshot of the receipt on the device, or a printed paper copy.
4. Male participants, and heterosexually active females of child-bearing potential, must practice adequate contraception for 30 days prior to the injection and must agree to continue adequate contraception until 180 days after the injection. Negative pregnancy test will be obtained from female participants of child-bearing potential at screening and at Day 0.
5. Provide a written informed consent for the study prior to performing any study-related procedure. The Investigator or a qualified designee must ensure the appropriate consent is in place.

Exclusion criteria

1. Presence of any febrile illness or any known or suspected acute illness on the day of immunization.

2. Clinically significant bleeding disorder (e.g., clotting factor deficiency, coagulopathy, or platelet disorder), or prior history of significant bleeding or bruising following intramuscular injection or venipuncture.

3. Presence of an autoimmune disease.

4. Receiving systemic steroids in doses exceeding 20mg daily of prednisone or equivalent, for ≥ 14 days within 1 month, or has recently received any other cytotoxic or immunosuppressive drug within 6 months prior to the injection of the study vaccine.

5. Has a known malignancy diagnosed within the past 5 years. Participants with basal cell carcinoma or squamous cell carcinoma of the skin are not excluded.

6. Currently receiving systemic immunomodulatory therapy or received chemotherapy within the last 5 years excluding topical agents.

7. Has received blood products or immunoglobulins (IVIg or IMIg) within 3 months of study entry/baseline serologic evaluation.

8. Currently on anti-tuberculosis therapy.

9. Had SARS-CoV-2 infection within 4 months prior to study Day 0. A potential participant is considered to have COVID-19 infection base on one of the following:

   • Positive polymerase chain reaction (PCR) or rapid antigen test.
   • Documentation in a medical history report.
   • Reported by candidate.

10. Has received any non-COVID-19 authorized vaccines (e.g., influenza) within 2 weeks prior to receiving study dose injection.

11. Has received any experimental SARS-CoV-2 / COVID-19 vaccines Receipt of SARSCoV-2/COVID-19 vaccines that were experimental at the time of administration but are currently authorized, more than 6 months prior to Day 0, will not lead to exclusion.

12. Planning to receive booster doses of any authorized COVID-19 vaccine during the first two months days from study vaccination.

13. Abnormal laboratory test results (hematology, biochemistry, and urinalysis) as compared to the local normal lab ranges. To exclude transient abnormalities, laboratory tests may be repeated once. Abnormal lab test results considered not clinically significant by the Investigator will not be exclusionary.

14. Has a history of any reaction or known sensitivity likely to be exacerbated by any component of the study vaccine.

15. Is currently participating in or has participated in a study of an investigational agent within 6 months prior to the injection of the booster vaccine under study.

16. A female is not eligible to participate if she is pregnant or breast feeding

17. Being a member of the study team, or an immediate family member or household member of a member on the study team.

18. Any condition, which in the opinion of the investigator may deem the participant inappropriate for the study.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Quadruple Blind

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47 participants in 4 patient groups, including a placebo group

COVAC-01 10µg group

Experimental group

Description:

12 healthy adults ≥18 years of age receive the vaccine on Day 0.

Treatment:

Biological: COVAC-1

COVAC-01 25µg group

Experimental group

Description:

12 healthy adults ≥18 years of age receive the vaccine on Day 0.

Treatment:

Biological: COVAC-1

COVAC-01 50µg group

Experimental group

Description:

12 healthy adults ≥18 years of age receive the vaccine on Day 0.

Treatment:

Biological: COVAC-1

Placebo Control

Placebo Comparator group

Description:

12 healthy adults ≥18 years of age receive a dose of normal saline (placebo) on Day 0.

Treatment:

Biological: Saline Placebo