First-in-human Study to Evaluate the Safety and Immunogenicity of Three Dose Levels of the OVX033 Coronavirus Vaccine Candidate in Healthy Volunteers

Coronavirus Clinical Trial

Official title:

A First-in-human Phase 1, Single Center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Immunogenicity of Three Dose Levels of the OVX033 Vaccine, After Intramuscular Administration in Healthy Subjects Aged 18-49 Years

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT06128382
• Other study ID #: OVX033-001
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: January 8, 2024
• Est. completion date: December 2024

Study information

• Verified date: June 2024
• Source: Osivax
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This first-in-human clinical trial is designed to evaluate the safety and immunogenicity of one administration of OVX033 coronavirus vaccine at different dose levels (100µg, 250µg and 500µg)

Description:

This trial is a first-in-human phase 1, single center, randomized, double-blind, placebo-controlled study in 48 adult subjects to evaluate the safety and immunogenicity of OVX033 sarbecovirus vaccine at different dose levels (100µg, 250µg and 500µg).

One single dose of OVX033 vaccine or of Placebo will be administered intramuscularly in healthy subjects aged 18-49 years.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 48
• Est. completion date: December 2024
• Est. primary completion date: July 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 49 Years

Eligibility

Inclusion Criteria:

1. Written informed consent.

2. Healthy male or female subjects, as determined by medical history and medical examination.

3. Aged 18 to 49 years.

4. Subjects who have been vaccinated (2 to 4 doses) with a licensed SARS-CoV-2 (COVID-19) vaccine. The last dose should be >6 months before administration of the investigational vaccine.

5. Reliable and willing to make themselves available for the duration of the study, willing and able to follow study procedures.

6. Willing to refrain from strenuous physical exercise during the week preceding any blood sampling, including between screening and vaccination visit (Visit 2).

Exclusion Criteria:

1. Subjects with a body mass index (BMI) <18 kg/m² or >30 kg/m² at screening.

2. Subjects weighing less than 50 kg.

3. Subjects with abnormal safety laboratory (hematology, biochemistry, coagulation and urinalysis) parameter at screening.

4. Subjects having previously received a non-licensed SARSCoV-2 vaccine or only one single dose of a licensed SARSCoV-2 vaccine.

5. Subjects having presented medically significant adverse event after having received a SARS-CoV-2 licensed vaccine.

6. Subjects currently treated with medications intended to prevent SARS-CoV-2 infection or disease (COVID-19) complications.

7. SARS-CoV-2 infection within the past 3 months prior to enrolment, RT-PCR-confirmed SARS-CoV-2 infection at screening or ongoing symptom of COVID-19.

8. Subjects having received another vaccination within 3 months prior to the day of study vaccination for live attenuated vaccines, or within 1 month prior to the day of study vaccination for inactivated vaccines.

9. Planning to receive other vaccines during the first 28 days following the study vaccine administration.

10. Female subjects: pregnant, breast-feeding or of childbearing potential without appropriate contraceptive methods in place for at least 2 months before enrolment, or with positive pregnancy test at screening or on the day of vaccination. Appropriate contraceptive methods are to be maintained until the end of the trial.

11. Subjects receiving treatment that can affect immune response such as systemic or high dose inhaled corticosteroids (>800µg/day beclomethasone or equivalent; occasional inhaled corticosteroids for asthma therapy are allowed), radiation treatment, cytotoxic drugs, or current or recent (within 3 months before study entry) chronic or prolonged (>10 days) use of systemic non-steroidal anti-inflammatory drugs, interferon, immunomodulators, allergy shots, as judged by the Investigator.

12. Any known or suspected immunodeficient conditions.

13. Past or current history of significant autoimmune diseases, as judged by the Investigator.

14. Known or suspected infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV), or hepatitis B virus (HBV) at screening.

15. Current history of medical illness such as diabetes, hypertension, heart, renal or hepatic diseases, as judged by the Investigator.

16. Hereditary or acquired hemorrhagic tendency or coagulation dysfunction (e.g., cytokine defects, coagulation disorders or platelet disorder), or history of serious bleeding, or history of massive bleeding after intramuscular injection, intravenous puncture or ecchymosis.

17. History of receiving blood, blood components or immunoglobulins within 3 months prior to the day of vaccination, or planned to receive such product during the whole study period.

18. Presence of an acute febrile illness on the day of planned vaccination or within 72 hours prior of it (oral temperature>38.0°C; temporary exclusion criterion).

19. Past or current history of any progressive or severe neurological disorder, seizure disorder or Guillain-Barré syndrome.

20. Behavioral or cognitive impairment, or psychiatric disease that, in the opinion of the Investigator, may interfere with the subject's ability to participate in the study.

21. Past (stopped less than 6 months before enrolment) or current smoking habit above 10 cigarettes per day.

22. Past (stopped less than 6 months before enrolment) or current history of alcohol consumption (more than 2 glasses per day, more than 10 glasses per week, or absence of any days within a week without consumption. A standard glass contains 10 g of alcohol corresponding to 10 cl of wine, 25 cl of beer at 5% or 3 cl of alcohol at 40% [Société Française d'Alcoologie, 2023]).

23. Past (stopped less than 6 months before enrolment) or current history of use of recreational drugs.

24. Prophylactic or therapeutic use of any anti(retro)virals by systemic route during the study. Topical application is allowed.

25. History of severe allergic reactions and/or anaphylaxis, or serious adverse reactions to vaccines or allergy to kanamycin.

26. Any contraindication to intramuscular administration, as judged by the Investigator.

27. Individuals with history of any illness that, in the opinion of the Investigator, might interfere with the results of the study, or pose additional risk to the subjects due to participation in the study, either directly or through any treatments administered for that illness.

28. Sponsor employees or Investigator site personnel directly affiliated with this study, and their immediate families. Immediate family is defined as a spouse (or assimilated), parent, child or sibling, whether biological or legally adopted.

29. Subjects receiving =10 mg/day of prednisone or equivalent for more than 3 months before study entry.

30. Health professionals and/or students for whom vaccination against SARS-CoV-2 is strongly recommended.

Related Conditions & MeSH terms

• Coronavirus
• Coronavirus Infections

Intervention

Biological:
• OVX033
One single administration intramuscularly on Day 1
• Saline solution
One single administration intramuscularly on Day 1

Locations

Country	Name	City	State
France	CIC Cochin Pasteur CIC 1417 Hôpital Cochin	Paris

Sponsors (2)

Lead Sponsor	Collaborator
Osivax	CIC 1417 Cochin Pasteur Hôpital Cochin Paris France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number and percentage of subjects reporting solicited local (Injection site redness, Injection site swelling, Injection site pain) and systemic (Fatigue, Headache, Arthralgia, Malaise, Myalgia, Fever) signs and symptoms		during 7 days after vaccine administration
Primary	Number and percentage of subjects reporting unsolicited adverse events		during 29 days after vaccine administration
Primary	Occurrence of adverse event of special interest		during the whole study duration, 180 days
Primary	Occurrence of serious adverse event		during the whole study duration, 180 days
Primary	Number and percentage of subjects with medically-attended adverse events (classified by type and reason)		during the whole study duration, 180 days
Primary	Number and percentage of subjects with deviations from normal values (judged clinically relevant or not by the Investigator) of safety laboratory tests		during 29 days after vaccine administration
Secondary	Cell-mediated immune response in terms of change of N-specific T-cell number in PBMCs, measured by IFN? ELISPOT (after in vitro stimulation)		at Days 8, 29, 90 and 180 versus pre-injection baseline (Day 1)
Secondary	N-specific CD4+ and CD8+T-cell percentages measured by flow cytometry (on PBMCs), identified as expressing markers (after in vitro stimulation), such as IL-2, TNFa and/or IFN?		at Day 1 (pre-injection baseline) and Days 8, 29, 90 and 180
Secondary	Geometric mean titers (GMTs) of anti-N IgG (ELISA, serum)		at Day 1 (pre-injection baseline), and Days 8, 29, 90 and 180
Secondary	Number and percentage of subjects with an increase (four-fold) in anti-N IgG titer		on Days 8, 29, 90 and 180, with respect to preinjection baseline (Day 1)
Secondary	Anti-OVX313 IgG (ELISA, serum) titers		at Days 29, 90 and 180 versus pre-injection baseline (Day 1)
Secondary	anti-hC4BP oligomerization domain IgG (ELISA, serum) titers [If positive result for anti-OVX313]		at Days 29, 90 and 180 versus pre-injection baseline (Day 1)
Secondary	Number and percentage of subjects with a RT-PCR-confirmed SARS-CoV-2 and/or influenza A or B infection		during the whole study duration, 180 days