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Phase 2 Completed N=668 Randomized Triple-blind Prevention

A Dose-Confirmation Study to Evaluate the Safety, Reactogenicity and Immunogenicity of Vaccine CVnCoV in Healthy Adults for COVID-19

Coronavirus · Covid19 · SARS-CoV-2 infection · Severe Acute Respiratory Syndrome
Source: ClinicalTrials.gov NCT04515147 ↗
Enrolled (actual)
668
Serious AEs
2.4%
Results posted
Sep 2023
Primary outcomePrimary: Number of Participants Who Experienced a Solicited Adverse Event (AE) Occurring on the Day of Vaccination and the Following 7 Days After Dose 1 and Dose 2 — 9; 5; 253; 220 Participants

Summary

This study aims to evaluate the safety and reactogenicity profile after 1 and 2 dose administrations of investigational SARS-CoV-2 mRNA vaccine (CVnCoV) at different dose levels and to evaluate the humoral immune response after 1 and 2 dose administrations of CVnCoV.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Who Experienced a Solicited Adverse Event (AE) Occurring on the Day of Vaccination and the Following 7 Days After Dose 1 and Dose 2
9; 5; 253; 220; 17; 26
PRIMARY
Intensity of Solicited AEs Per US Food and Drug Administration (FDA) Toxicity Grading Scale Occurring on the Day of Vaccination and the Following 7 Days After Dose 1 and Dose 2
9; 5; 191; 203; 16; 25
PRIMARY
Duration of Solicited AEs Occurring on the Day of Vaccination and the Following 7 Days After After Dose 1 and Dose 2
1.3; 1.2; 2.1; 1.8; 1.6; 2.0
PRIMARY
Number of Participants Who Experienced an Unsolicited AE Occurring on the Day of Vaccination and the Following 28 Days After Dose 1 and Dose 2
5; 6; 120; 105; 7; 5
PRIMARY
Intensity of Unsolicited AEs Per the Investigator's Assessment Occurring on the Day of Vaccination and the Following 28 Days After Dose 1 and Dose 2
3; 6; 94; 88; 6; 4
PRIMARY
Number of Participants Who Experienced a Serious Adverse Event (SAE) During the Trial
0; 1; 8; 6; 0; 1
PRIMARY
Number of Participants Who Experienced an Adverse Event of Special Interest (AESI) During the Trial
1; 3; 36; 23; 7; 3
PRIMARY
Percentage of Participants Seroconverting for SARS-CoV-2 Spike Protein Receptor-Binding Domain (RBD) Antibodies on Day 29 and Day 43
0; 10.0; 11.6; 7.8; 0; 4.3
PRIMARY
Geometric Mean Titers (GMTs) of SARS-CoV-2 Spike Protein RBD Antibodies on Day 29 and Day 43
50.000; 57.154; 67.221; 63.828; 56.724; 52.112
PRIMARY
Percentage of Participants Seroconverting for SARS-CoV-2 Neutralizing Antibodies on Day 29 and Day 43
0; 0; 8.3; 7.8; 0; 0
PRIMARY
GMTs of SARS-CoV-2 Neutralizing Antibodies on Day 29 and Day 43
5.000; 5.000; 5.912; 6.234; 5.000; 5.000
SECONDARY
Number of Participants Who Experienced a Solicited Adverse Event (AE) Occurring on the Day of Booster Vaccination and the Following 7 Days
15; 24; 12; 15; 24; 8
SECONDARY
Intensity of Solicited AEs Per FDA Toxicity Grading Scale Occurring on the Day of Booster Vaccination and the Following 7 Days
14; 18; 9; 1; 5; 3
SECONDARY
Duration of Solicited AEs Occurring on the Day of Booster Vaccination and the Following 7 Days
1.7; 2.0; 1.6; 2.8; 2.0; 2.0
SECONDARY
Number of Participants Who Experienced an Unsolicited AE Occurring on the Day of Booster Vaccination and the Following 28 Days
7; 6; 2; 1; 4; 2
SECONDARY
Intensity of Unsolicited AEs Per the Investigator's Assessment Occurring on the Day of Booster Vaccination and the Following 28 Days
6; 5; 2; 1; 0; 0
SECONDARY
Percentage of Participants Seroconverting for SARS-CoV-2 Spike Protein RBD Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393
82.1; 100; 100; 90.5; 69.2; 100
SECONDARY
GMTs of SARS-CoV-2 Spike Protein RBD Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393
516.198; 2889.963; 1449.055; 445.661; 153.160; 10094.652
SECONDARY
Percentage of Participants Seroconverting for SARS-CoV-2 Neutralizing Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393
75.0; 96.0; 57.1; 28.6; 7.7; 100
SECONDARY
GMTs of SARS-CoV-2 Neutralizing Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393
25.937; 74.642; 16.957; 7.308; 5.867; 141.724

Eligibility Criteria

Inclusion Criteria

  • Healthy male and female participants ≥18 years of age. A healthy participant is defined as an individual who is in good general health, according to the Investigator's assessment. Chronic health conditions are acceptable if the condition is considered well controlled with treatment according to the discretion of the Investigator.
  • Expected to be compliant with protocol procedures and available for clinical follow-up through the last planned visit.
  • Participants are able to understand and willing to provide informed consent.
  • Physical examination without clinically significant findings according to the Investigator's assessment.
  • Body mass index (BMI) ≥18.0 and ≤32.0 kg/m^2.
  • Female participants of childbearing potential: at the time of enrollment, negative human chorionic gonadotropin (hCG) pregnancy test (serum) for female participants presumed to be of childbearing potential on the day of enrollment. On Day 1 (pre-vaccination): negative urine pregnancy test (required if serum pregnancy test was performed more than 3 days before).
  • Female participants of childbearing potential must use highly effective methods of birth control from 2 weeks before the first administration of the trial vaccine until 3 months following the last administration. The following methods of birth control are considered highly effective when used consistently and correctly:
  • Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal or transdermal);
  • Progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable or implantable);
  • Intrauterine devices;
  • Intrauterine hormone-releasing systems;
  • Bilateral tubal occlusion;
  • Vasectomized partner;
  • Sexual abstinence (periodic abstinence [e.g., calendar, ovulation, symptothermal and post-ovulation methods] and withdrawal are not acceptable).
  • Male participants should be instructed not to get their partners pregnant until 3 months after the last administration.

Exclusion Criteria

  • Use of any investigational or non-registered product (vaccine or drug) other than the trial vaccine within 28 days preceding the administration of the trial vaccine, or planned use during the trial period.
  • Receipt of any other vaccines within 28 days prior to enrollment in this trial or planned receipt of any vaccine within 28 days of trial vaccine administration (primary dose or booster dose).
  • Receipt of any investigational or licensed/authorized SARS-CoV-2 or other coronavirus vaccine prior to the administration of the trial vaccine.
  • Any treatment with immunosuppressants or other immune-modifying drugs (including, but not limited to, corticosteroids, biologicals, and methotrexate) within 6 months prior to the administration of the trial vaccine or planned use during the trial, with the exception of topically-applied, inhaled, or intranasal steroids.
  • Use of hormonal therapy for gender reassignment.
  • Any medically diagnosed or suspected immunosuppressive or immunodeficient condition based on medical history and physical examination, including known human immunodeficiency virus infection, hepatitis B virus infection, and hepatitis C virus infection.
  • History of immune-mediated or autoimmune disease.
  • History of angioedema (known C1 inhibitor deficiency).
  • History of anaphylaxis or allergy to any component of CVnCoV or aminoglycoside antibiotics.
  • History of or current alcohol and/or drug abuse.
  • Participants who are active smokers, were active smokers within the last year (including any vaping in the last year), or have a total smoking history ≥10 pack years. A pack year is calculated by multiplying the number of packs of cigarettes smoked per day by the number of years the person has smoked.
  • History of virologically-confirmed Severe Acute Respiratory Syndrome (SARS), Middle East Respiratory Syndrome (MERS), or COVID-19 disease or known exposure (without any personal protec
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04515147). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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