Study of a Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) Adjuvanted Inactivated Vaccine in Healthy Adults

Overview

This phase I study is designed as double-blinded, randomised, placebo controlled, three-armed study composed of two different dose arms of protective adjuvanted inactivated vaccine against SARS-CoV-2 in dose escalations (first low dose group, followed by high dose group) and placebo arm.

Full Title of Study: “Phase I Study Evaluating the Safety and Efficacy of the Protective Adjuvanted Inactivated Vaccine Developed Against SARS-CoV-2 in Healthy Participants, Administered as Two Injections Subcutaneously in Two Different Dosages.”

Study Type

• Study Type: Interventional
• Study Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Primary Purpose: Prevention
  • Masking: Double (Participant, Investigator)
• Study Primary Completion Date: September 5, 2021

Detailed Description

This phase I study is designed as double-blinded, randomised, placebo controlled, three-armed study composed of two different dose arms of protective adjuvanted inactivated vaccine against SARS-CoV-2 in dose escalations (first low dose group, followed by high dose group) and placebo arm. Each dose of vaccine will be defined as a cohort in itself, with vaccine administration to 20 participants and placebo administration to 5 participants. After completion of low-dose group, decision of switch to high-dose will be taken by the Independent Data Monitoring Committee and will continue accordingly. In the study, 50 healthy participants of 18-45 years of age will be recruited. All injections will be done subcutaneously. Injections will be administered at 1 and 21 days. The participants will be followed for 6 months and the study will be completed in 12 months.

Interventions

• Biological: SARS-CoV-2 vaccine
  • Adjuvanted inactivated vaccine
• Biological: Placebo
  • 0.9% NaCl

Arms, Groups and Cohorts

• Experimental: Low-Dose Group (Group A)
  • 20 participants will receive 10 µg-3M inactivated virus + 1 mg Al(OH)3 + 300 µg CpGODN adjuvanted vaccine
• Experimental: High-Dose Group (Group B)
  • 20 participants will receive 20 µg-6M inactivated virus + 1 mg Al(OH)3 + 300 µg CpGODN adjuvanted vaccine
• Placebo Comparator: Placebo Group
  • 10 participants will receive 1 ml of 0.9% sodium chloride (NaCl)

Clinical Trial Outcome Measures

Primary Measures

• Acute adverse events (AEs)
  • Time Frame: 24 hours
  • Frequency of acute adverse events in all dosage groups
• Solicited local and systemic adverse events (AEs)
  • Time Frame: 15 days
  • Frequency of local and systemic AEs in all dosage groups
• Unsolicited local and systemic adverse events (AEs)
  • Time Frame: 28 days
  • Frequency of local and systemic AEs in all dosage groups

Secondary Measures

• Neutralizing antibody response
  • Time Frame: Before first dose administration, on Day 21-28-35 and Month 3 and Month 6 after first dose administration.
  • Immunogenicity response by measuring neutralizing antibody titer (anti-spike and anti-RBD) developed against SARS-CoV-2 (by ELISA)
• Cellular immune response
  • Time Frame: Before first dose administration, on Day 21-28-35 and Month 3 and Month 6 after first dose administration.
  • Interferon-γ (IFN-γ) positive cell level (by ELISPOT)

Participating in This Clinical Trial

Inclusion Criteria

To be eligible for the study, each participant must satisfy all the following criteria: 1. Healthy participants between 18-45 years of age, 2. Sign an informed consent document, 3. Negative immunoglobulin G (IgG) and immunoglobulin M (IgM) antibody for COVID-19, 4. Negative quantitative polymerase chain reaction (qPCR) SARS-CoV-2 results of nasopharyngeal/sputum samples, 5. Able to comply with the study protocol during the study period, 6. Negative tests for Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), 7. Body temperature <37.2 C and no signs of active infection, 8. Body mass index 18-35 kg/m2, 9. Normal laboratory levels of whole blood count, alanine transaminase (ALT), aspartate transaminase (AST), total bilirubin, urea, creatinine, and fasting blood glucose, or abnormal finding detected in any laboratory parameter which is not greater than Grade 1 according to the investigator's evaluation, 10. Good general health (no known disease in the history and physical examination within 14 days prior to the enrolment), 11. Female and male participants who will be able to have appropriate contraception methods within 30 days prior to vaccine injection and within 6 months after vaccination, Exclusion Criteria:

Participants with any of the following criteria will be excluded: 1. History of seizure, encephalopathy, or psychosis, 2. History of allergic reactions to any known vaccine or to any component of the study vaccine, 3. Pregnant, breastfeeding, or positive pregnancy test or planning to conceive within 6 months, 4. History of SARS-CoV-2 infection, 5. Severe cardiovascular disorders (arrhythmia, conduction disorders, history of myocardial infarction, uncontrolled hypertension), 6. Severe chronic disorders (asthma, diabetes mellitus, thyroid disorders…etc), 7. Congenital or acquired angioedema, 8. Diagnosis of immunodeficiency, 9. Diagnosis of bleeding diathesis, 10. Use of immunosuppressive treatment, anti-allergic treatment, cytotoxic treatment, inhaler corticosteroids (allergic rhinitis or topical steroid ointments are excluded), 11. Those who received blood and blood product transfusions in the last 6 months, 12. Those on any vaccine program or experimental medication within 1 month prior to the study, 13. History of any vaccination against SARS-CoV-2 within 1 month prior to the study, 14. Use of active tuberculosis treatment, 15. History of addictive drug use, 16. History of alcohol abuse and/or history of alcohol intake more than 2 units per day or 10 units per week and/or positive breath alcohol test (one unit of alcohol equals to 250 mL beer, 125 mL wine or 25 mL whiskey), 17. According to the investigator's evaluation, those who have any condition (medical, psychological, social, etc.) that may impair the patient's compliance with the study will be excluded from the study.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 45 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

• Lead Sponsor
  • Osman ERGANIS, PhD, Prof
• Collaborator
  • The Scientific and Technological Research Council of Turkey
• Provider of Information About this Clinical Study
  • Sponsor-Investigator: Osman ERGANIS, PhD, Prof, PhD, Prof – The Scientific and Technological Research Council of Turkey
• Overall Official(s)
  • Oguz Akbas, MD, Study Director, MonitorCRO