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| Name | Class |
|---|---|
| German Federal Ministry of Education and Research | OTHER_GOV |
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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.
This clinical trial information was submitted voluntarily under the applicable law and, therefore, certain submission deadlines may not apply. (That is, clinical trial information for this applicable clinical trial was submitted under section 402(j)(4)(A) of the Public Health Service Act and 42 CFR 11.60 and is not subject to the deadlines established by sections 402(j)(2) and (3) of the Public Health Service Act or 42 CFR 11.24 and 11.44.).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Part 1, Group 1: CVnCoV 6 μg | Experimental | Participants will be vaccinated with CVnCoV on Day 1 and Day 29. Participants in this group will be aged between 18 and 60 years old. |
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| Part 1, Group 2: CVnCoV 6 μg | Experimental | Participants will be vaccinated with CVnCoV on Day 1 and Day 29. Participants in this group will be aged over 60 years old. |
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| Part 1, Group 3: CVnCoV 12 μg | Experimental | Participants will be vaccinated with CVnCoV on Day 1 and Day 29. Participants in this group will be between the ages of 18 to 60 years old. CVnCoV will be administered again as a booster vaccination on Day 180 in a sub-group of participants. |
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| Part 1, Group 4: CVnCoV 12 μg | Experimental | Participants will be vaccinated with CVnCoV on Day 1 and Day 29. Participants in this group will be aged over 60 years old. CVnCoV will be administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants. |
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| Part 1, Group 5: Hepatitis A vaccine | Active Comparator | Participants will be vaccinated with a hepatitis A vaccine on Day 1 and Day 29. Participants in this group will be aged between 18 and 60 years old. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CVnCoV 6 μg | Biological | Participants will receive an intramuscular injection by needle in the deltoid area. |
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| Measure | Description | Time Frame |
|---|---|---|
| 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 | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). By definition, all solicited local AEs occurring from the time of first vaccination were considered related to trial vaccination. For solicited systemic AEs, the Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Up to 7 days after Dose 1 (Days 1 to 8) and Dose 2 (Days 29 to 36) |
| 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 | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Intensity of solicited local AEs and solicited systemic AEs were graded per the FDA Toxicity Grading Scale at Grades 1-3, where higher grades indicate a worse outcome. | Up to 7 days after Dose 1 (Days 1 to 8) and Dose 2 (Days 29 to 36) |
| Duration of Solicited AEs Occurring on the Day of Vaccination and the Following 7 Days After After Dose 1 and Dose 2 | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Duration is calculated as consecutive days with a respective solicited AE regardless of the grade of the AE. AEs ongoing after day 8 are included. | Up to 7 days after Dose 1 (Days 1 to 8) and Dose 2 (Days 29 to 36) |
| 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 |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants Who Experienced a Solicited Adverse Event (AE) Occurring on the Day of Booster Vaccination and the Following 7 Days | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). By definition, all solicited local AEs occurring from the time of first vaccination were considered related to trial vaccination. For solicited systemic AEs, the Investigator assessed the relationship between trial vaccine and each occurrence of each AE. |
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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:
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 protective equipment) to an individual with confirmed COVID-19 disease or SARS-CoV-2 infection within the past 2 weeks.
Administration of immunoglobulins and/or any blood products within the 3 months preceding the administration of any dose of the trial vaccine.
Presence or evidence of significant uncontrolled acute or chronic medical or psychiatric illness. Significant medical or psychiatric illnesses include but are not limited to:
Foreseeable non-compliance with protocol, as judged by the Investigator.
For female participants: pregnancy or lactation.
Participants with impaired coagulation or any bleeding disorder in whom an intramuscular injection or a blood draw is contraindicated. This includes participants on treatment with anticoagulants (e.g., vitamin K antagonists, novel oral anticoagulants, and heparin). Use of platelet aggregation inhibitors is not exclusionary.
Participants employed by the Sponsor, Investigator, or trial site, or relatives of research staff working on this trial.
Participants considered at the Investigator's discretion to be at increased risk of exposure to COVID-19 disease.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centro de vacunación internacional - CEVAXIN Panama Clinic | Panama City | 0831 | Panama | |||
| Instituto de Investigación Nutricional |
Of the 1035 participants who were screened, 668 participants were enrolled and received trial vaccine.
This trial was performed in Peru and Panama between 21 September 2020 and 21 February 2022.
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| ID | Title | Description |
|---|---|---|
| FG000 | CVnCoV 6 μg: Aged 18-60 Years | Participants in Part 1 were vaccinated with CVnCoV 6 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| FG001 | CVnCoV 6 μg: Aged >60 Years |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Dec 3, 2021 | Oct 3, 2022 |
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| Part 1, Group 6: Pneumococcal vaccine | Active Comparator | Participants will be vaccinated with a pneumococcal vaccine on Day 1 and Day 29. Participants in this group will be aged over 60 years old. |
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| Part 2, Group 1: CVnCoV 12 µg | Experimental | Participants will be vaccinated with CVnCoV 12 µg on Day 1 and Day 29. Participants in this group will be aged between 18 and 60 years old. |
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| Part 2, Group 2: Hepatitis A vaccine | Active Comparator | Participants will be vaccinated with a hepatitis A vaccine on Day 1 and Day 29. Participants in this group will be aged between 18 and 60 years old. |
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| Part 2, Group 3: CVnCoV 12 µg | Experimental | Participants will be vaccinated with CVnCoV 12 µg on Day 1 and Day 29. Participants in this group will be aged over 60 years old. |
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| Part 2, Group 4: Pneumococcal vaccine | Active Comparator | Participants will be vaccinated with a pneumococcal vaccine on Day 1 and Day 29. Participants in this group will be aged over 60 years old. |
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| CVnCoV 12 μg | Biological | Participants will receive an intramuscular injection by needle in the deltoid area. |
|
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| Hepatitis A vaccine | Biological | Participants will receive an intramuscular injection by needle in the deltoid area. |
|
| Pneumococcal vaccine | Biological | Participants will receive an intramuscular injection by needle in the deltoid area. |
|
| CVnCoV 12μg | Biological | Participants will receive an intramuscular injection by needle in the deltoid area. |
|
|
Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. |
| Up to 28 days after Dose 1 (Days 1 to 29) and Dose 2 (Days 29 to 57) |
| 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 | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator made an assessment of intensity for each AE reported during the trial and assigned it to one of the following categories:
| Up to 28 days after Dose 1 (Days 1 to 29) and Dose 2 (Days 29 to 57) |
| Number of Participants Who Experienced a Serious Adverse Event (SAE) During the Trial | An SAE was defined as any untoward medical occurrence that, at any dose:
The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Up to Day 393 |
| Number of Participants Who Experienced an Adverse Event of Special Interest (AESI) During the Trial | AESIs included:
Participants who became unblinded and/or received a licensed/authorized vaccine were censored at the day after unblinding or at the day after receiving the licensed/authorized vaccine, whichever was earlier. The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Up to Day 393 |
| Percentage of Participants Seroconverting for SARS-CoV-2 Spike Protein Receptor-Binding Domain (RBD) Antibodies on Day 29 and Day 43 | As measured by enzyme-linked immunosorbent assay (ELISA). In participants not exposed to SARS-CoV-2 before the trial seroconversion was defined as any increase in titer in antibodies against SARS-CoV-2 RBD versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | Baseline, Day 29 and Day 43 |
| Geometric Mean Titers (GMTs) of SARS-CoV-2 Spike Protein RBD Antibodies on Day 29 and Day 43 | As measured by ELISA. The SARS-CoV-2 spike RBD protein-specific antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | Day 29 and Day 43 |
| Percentage of Participants Seroconverting for SARS-CoV-2 Neutralizing Antibodies on Day 29 and Day 43 | As measured by an activity assay. In participants not exposed to SARS-CoV-2 before the trial, seroconversion was defined as any increase in titer in SARS-CoV-2 neutralizing antibodies versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | Baseline, Day 29 and Day 43 |
| GMTs of SARS-CoV-2 Neutralizing Antibodies on Day 29 and Day 43 | The SARS-CoV-2 neutralizing antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | Day 29 and Day 43 |
| Up to 7 days after booster vaccination (Days 57 to 64 and Days 180 to 187) |
| Intensity of Solicited AEs Per FDA Toxicity Grading Scale Occurring on the Day of Booster Vaccination and the Following 7 Days | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Intensity of solicited local AEs and solicited systemic AEs were graded per the FDA Toxicity Grading Scale at Grades 1-3, where higher grades indicate a worse outcome. | Up to 7 days after booster vaccination (Days 57 to 64 and Days 180 to 187) |
| Duration of Solicited AEs Occurring on the Day of Booster Vaccination and the Following 7 Days | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Duration is calculated as consecutive days with a respective solicited AE regardless of the grade of the adverse event. | Up to 7 days after booster vaccination (Days 57 to 64 and Days 180 to 187) |
| Number of Participants Who Experienced an Unsolicited AE Occurring on the Day of Booster Vaccination and the Following 28 Days | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Up to 28 days after booster vaccination (Days 57 to 85 and Days 180 to 208) |
| Intensity of Unsolicited AEs Per the Investigator's Assessment Occurring on the Day of Booster Vaccination and the Following 28 Days | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator made an assessment of intensity for each AE reported during the trial and assigned it to one of the following categories:
| Up to 28 days after booster vaccination (Days 57 to 85 and Days 180 to 208) |
| Percentage of Participants Seroconverting for SARS-CoV-2 Spike Protein RBD Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by ELISA. In participants not exposed to SARS-CoV-2 before the trial seroconversion was defined as any increase in titer in antibodies against SARS-CoV-2 RBD versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | For participants who received the booster vaccination on Day 57: Baseline, Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Baseline, Day 180, Day 208 and Day 393 |
| GMTs of SARS-CoV-2 Spike Protein RBD Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by ELISA. The SARS-CoV-2 spike RBD protein-specific antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | For participants who received the booster vaccination on Day 57: Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Day 180, Day 208 and Day 393 |
| Percentage of Participants Seroconverting for SARS-CoV-2 Neutralizing Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by an activity assay. In participants not exposed to SARS-CoV-2 before the trial, seroconversion was defined as any increase in titer in SARS-CoV-2 neutralizing antibodies versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | For participants who received the booster vaccination on Day 57: Baseline, Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Baseline, Day 180, Day 208 and Day 393 |
| GMTs of SARS-CoV-2 Neutralizing Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by an activity assay. The SARS-CoV-2 neutralizing antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | For participants who received the booster vaccination on Day 57: Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Day 180, Day 208 and Day 393 |
| Lima |
| Lima - 12 |
| Peru |
Participants in Part 1 were vaccinated with CVnCoV 6 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
| FG002 | CVnCoV 12 μg: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| FG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| FG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| FG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
| COMPLETED |
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| NOT COMPLETED |
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Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available.
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| ID | Title | Description |
|---|---|---|
| BG000 | CVnCoV 6 μg: Aged 18-60 Years | Participants in Part 1 were vaccinated with CVnCoV 6 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| BG001 | CVnCoV 6 μg: Aged >60 Years | Participants in Part 1 were vaccinated with CVnCoV 6 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
| BG002 | CVnCoV 12 μg: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| BG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| BG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| BG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
| BG006 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Ethnicity (NIH/OMB) | Count of Participants | Participants |
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| Race/Ethnicity, Customized | Count of Participants | Participants |
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| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). By definition, all solicited local AEs occurring from the time of first vaccination were considered related to trial vaccination. For solicited systemic AEs, the Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available. Only participants with evaluable samples at each visit are included. | Posted | Count of Participants | Participants | Up to 7 days after Dose 1 (Days 1 to 8) and Dose 2 (Days 29 to 36) |
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| 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 | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Intensity of solicited local AEs and solicited systemic AEs were graded per the FDA Toxicity Grading Scale at Grades 1-3, where higher grades indicate a worse outcome. | The Safety Analysis Set including only participants who experienced solicited local and systemic AEs. Only participants with evaluable samples at each visit are included. | Posted | Count of Participants | Participants | Up to 7 days after Dose 1 (Days 1 to 8) and Dose 2 (Days 29 to 36) |
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| Primary | Duration of Solicited AEs Occurring on the Day of Vaccination and the Following 7 Days After After Dose 1 and Dose 2 | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Duration is calculated as consecutive days with a respective solicited AE regardless of the grade of the AE. AEs ongoing after day 8 are included. | The Safety Analysis Set including only participants who experienced solicited local and systemic AEs. Only participants with evaluable samples at each visit are included. | Posted | Mean | Standard Deviation | days | Up to 7 days after Dose 1 (Days 1 to 8) and Dose 2 (Days 29 to 36) |
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| 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 | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available. Only participants with evaluable samples at each visit are included. | Posted | Count of Participants | Participants | Up to 28 days after Dose 1 (Days 1 to 29) and Dose 2 (Days 29 to 57) |
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| 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 | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator made an assessment of intensity for each AE reported during the trial and assigned it to one of the following categories:
| The Safety Analysis Set including only participants who experienced unsolicited AEs. Only participants with evaluable samples at each visit are included. | Posted | Count of Participants | Participants | Up to 28 days after Dose 1 (Days 1 to 29) and Dose 2 (Days 29 to 57) |
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| Primary | Number of Participants Who Experienced a Serious Adverse Event (SAE) During the Trial | An SAE was defined as any untoward medical occurrence that, at any dose:
The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available. Only participants with evaluable samples at each visit are included. | Posted | Count of Participants | Participants | Up to Day 393 |
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| Primary | Number of Participants Who Experienced an Adverse Event of Special Interest (AESI) During the Trial | AESIs included:
Participants who became unblinded and/or received a licensed/authorized vaccine were censored at the day after unblinding or at the day after receiving the licensed/authorized vaccine, whichever was earlier. The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available. Only participants with evaluable samples at each visit are included. | Posted | Count of Participants | Participants | Up to Day 393 |
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| Primary | Percentage of Participants Seroconverting for SARS-CoV-2 Spike Protein Receptor-Binding Domain (RBD) Antibodies on Day 29 and Day 43 | As measured by enzyme-linked immunosorbent assay (ELISA). In participants not exposed to SARS-CoV-2 before the trial seroconversion was defined as any increase in titer in antibodies against SARS-CoV-2 RBD versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1 and Dose 2 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Number | 95% Confidence Interval | percentage of participants | Baseline, Day 29 and Day 43 |
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| Primary | Geometric Mean Titers (GMTs) of SARS-CoV-2 Spike Protein RBD Antibodies on Day 29 and Day 43 | As measured by ELISA. The SARS-CoV-2 spike RBD protein-specific antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1 and Dose 2 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Geometric Mean | Standard Deviation | titers | Day 29 and Day 43 |
| |||||||||||||||||||||||||||||||||||||
| Primary | Percentage of Participants Seroconverting for SARS-CoV-2 Neutralizing Antibodies on Day 29 and Day 43 | As measured by an activity assay. In participants not exposed to SARS-CoV-2 before the trial, seroconversion was defined as any increase in titer in SARS-CoV-2 neutralizing antibodies versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1 and Dose 2 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Number | 95% Confidence Interval | percentage of participants | Baseline, Day 29 and Day 43 |
| |||||||||||||||||||||||||||||||||||||
| Primary | GMTs of SARS-CoV-2 Neutralizing Antibodies on Day 29 and Day 43 | The SARS-CoV-2 neutralizing antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1 and Dose 2 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Geometric Mean | Standard Deviation | titers | Day 29 and Day 43 |
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| Secondary | Number of Participants Who Experienced a Solicited Adverse Event (AE) Occurring on the Day of Booster Vaccination and the Following 7 Days | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). By definition, all solicited local AEs occurring from the time of first vaccination were considered related to trial vaccination. For solicited systemic AEs, the Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available. Only participants who received a booster vaccination on Day 57 or Day 180 and had evaluable samples at each visit were included. | Posted | Count of Participants | Participants | Up to 7 days after booster vaccination (Days 57 to 64 and Days 180 to 187) |
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| Secondary | Intensity of Solicited AEs Per FDA Toxicity Grading Scale Occurring on the Day of Booster Vaccination and the Following 7 Days | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Intensity of solicited local AEs and solicited systemic AEs were graded per the FDA Toxicity Grading Scale at Grades 1-3, where higher grades indicate a worse outcome. | The Safety Analysis Set including only participants who experienced solicited local and systemic AEs. Only participants who received a booster vaccination on Day 57 or Day 180 and had evaluable samples at each visit were included. | Posted | Count of Participants | Participants | Up to 7 days after booster vaccination (Days 57 to 64 and Days 180 to 187) |
| ||||||||||||||||||||||||||||||||||||||
| Secondary | Duration of Solicited AEs Occurring on the Day of Booster Vaccination and the Following 7 Days | Solicited local AEs (injection site pain, redness, swelling, and itching) and solicited systemic AEs (fever, headache, fatigue, chills, myalgia, arthralgia, nausea/vomiting, and diarrhea) were recorded on the day of vaccination and the following 7 days using a diary (electronic or paper). Duration is calculated as consecutive days with a respective solicited AE regardless of the grade of the adverse event. | The Safety Analysis Set including only participants who experienced solicited local and systemic AEs. Only participants who received a booster vaccination on Day 57 or Day 180 and had evaluable samples at each visit were included. | Posted | Mean | Standard Deviation | days | Up to 7 days after booster vaccination (Days 57 to 64 and Days 180 to 187) |
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| Secondary | Number of Participants Who Experienced an Unsolicited AE Occurring on the Day of Booster Vaccination and the Following 28 Days | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator assessed the relationship between trial vaccine and each occurrence of each AE. | Safety Analysis Set: All participants who received at least 1 dose of trial vaccine and for whom any post-vaccination safety data are available. Only participants who received a booster vaccination on Day 57 or Day 180 and had evaluable samples at each visit were included. | Posted | Count of Participants | Participants | Up to 28 days after booster vaccination (Days 57 to 85 and Days 180 to 208) |
| ||||||||||||||||||||||||||||||||||||||
| Secondary | Intensity of Unsolicited AEs Per the Investigator's Assessment Occurring on the Day of Booster Vaccination and the Following 28 Days | Diaries were used for collection of unsolicited AEs on each vaccination day and the following 28 days. In addition, participants received a prompt (by e.g., a phone call or text message) to verify whether the participants had any health concerns since the last visit. The Investigator made an assessment of intensity for each AE reported during the trial and assigned it to one of the following categories:
| The Safety Analysis Set including only participants who experienced unsolicited AEs. Only participants who received a booster vaccination on Day 57 or Day 180 and had evaluable samples at each visit were included. | Posted | Count of Participants | Participants | Up to 28 days after booster vaccination (Days 57 to 85 and Days 180 to 208) |
| ||||||||||||||||||||||||||||||||||||||
| 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 | As measured by ELISA. In participants not exposed to SARS-CoV-2 before the trial seroconversion was defined as any increase in titer in antibodies against SARS-CoV-2 RBD versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1, Dose 2 and a booster dose on Day 57 or Day 180 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Number | 95% Confidence Interval | percentage of participants | For participants who received the booster vaccination on Day 57: Baseline, Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Baseline, Day 180, Day 208 and Day 393 |
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| Secondary | GMTs of SARS-CoV-2 Spike Protein RBD Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by ELISA. The SARS-CoV-2 spike RBD protein-specific antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1, Dose 2 and a booster dose on Day 57 or Day 180 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Geometric Mean | Standard Deviation | titers | For participants who received the booster vaccination on Day 57: Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Day 180, Day 208 and Day 393 |
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| Secondary | Percentage of Participants Seroconverting for SARS-CoV-2 Neutralizing Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by an activity assay. In participants not exposed to SARS-CoV-2 before the trial, seroconversion was defined as any increase in titer in SARS-CoV-2 neutralizing antibodies versus baseline. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1, Dose 2 and a booster dose on Day 57 or Day 180 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Number | 95% Confidence Interval | percentage of participants | For participants who received the booster vaccination on Day 57: Baseline, Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Baseline, Day 180, Day 208 and Day 393 |
| |||||||||||||||||||||||||||||||||||||
| Secondary | GMTs of SARS-CoV-2 Neutralizing Antibodies on Day 57, Day 85, Day 180, Day 208 and Day 393 | As measured by an activity assay. The SARS-CoV-2 neutralizing antibodies are expressed as GMT (geometric mean of reciprocal duplicate dilutions). Concentration/titers marked as below the lower limit of quantification (LLOQ) were arbitrary replaced by half of the LLOQ for GMT computations purpose. Participants who received a licensed/authorized vaccine were censored at the day after receiving the licensed/ authorized vaccine. | The Immunogenicity Set including only participants who received Dose 1, Dose 2 and a booster dose on Day 57 or Day 180 with no protocol deviations with impact to immunogenicity, who did not get exposed to SARS-CoV-2 before the trial, or during the trial before the applicable sample was collected and had a blood sample collected at Day 43. | Posted | Geometric Mean | Standard Deviation | titers | For participants who received the booster vaccination on Day 57: Day 57, Day 85 and Day 180. For participants who received the booster vaccination on Day 180: Day 180, Day 208 and Day 393 |
|
Day 1 to Day 393
Adverse events were collected based on intervention type and were not collected separately for the active control arm.
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | CVnCoV 6 μg | Participants in Part 1 were vaccinated with CVnCoV 6 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. | 0 | 23 | 1 | 23 | 21 | 23 |
| EG001 | CVnCoV 12 μg | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. | 3 | 584 | 14 | 584 | 567 | 584 |
| EG002 | Active Control | Participants in Part 1 and Part 2 were vaccinated with an active control (hepatitis A vaccine if aged 18-60 years old or pneumococcal vaccine if aged over 60 years old) as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. | 1 | 61 | 1 | 61 | 59 | 61 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Appendicitis | Infections and infestations | 24.0 | Systematic Assessment |
| |
| COVID-19 | Infections and infestations | 24.0 | Systematic Assessment |
| |
| COVID-19 pneumonia | Infections and infestations | 24.0 | Systematic Assessment |
| |
| Extraocular muscle paresis | Eye disorders | 24.0 | Systematic Assessment |
| |
| Retinal vein occlusion | Eye disorders | 24.0 | Systematic Assessment |
| |
| Cholecystitis acute | Hepatobiliary disorders | 24.0 | Systematic Assessment |
| |
| Clavicle fracture | Injury, poisoning and procedural complications | 24.0 | Systematic Assessment |
| |
| Multiple injuries | Injury, poisoning and procedural complications | 24.0 | Systematic Assessment |
| |
| Wrist fracture | Injury, poisoning and procedural complications | 24.0 | Systematic Assessment |
| |
| Ovarian cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | 24.0 | Systematic Assessment |
| |
| Rectal adenocarcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | 24.0 | Systematic Assessment |
| |
| Pancreatitis acute | Gastrointestinal disorders | 24.0 | Systematic Assessment |
| |
| Ischaemic stroke | Nervous system disorders | 24.0 | Systematic Assessment |
| |
| Urticaria | Skin and subcutaneous tissue disorders | 24.0 | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Injection site pain | General disorders | 24.0 | Systematic Assessment |
| |
| Fatigue | General disorders | 24.0 | Systematic Assessment |
| |
| Chills | General disorders | 24.0 | Systematic Assessment |
| |
| Pyrexia | General disorders | 24.0 | Systematic Assessment |
| |
| Swelling | General disorders | 24.0 | Systematic Assessment |
| |
| Discomfort | General disorders | 24.0 | Systematic Assessment |
| |
| Injection site swelling | General disorders | 24.0 | Systematic Assessment |
| |
| Headache | Nervous system disorders | 24.0 | Systematic Assessment |
| |
| Myalgia | Musculoskeletal and connective tissue disorders | 24.0 | Systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | 24.0 | Systematic Assessment |
| |
| Back pain | Musculoskeletal and connective tissue disorders | 24.0 | Systematic Assessment |
| |
| Nasopharyngitis | Infections and infestations | 24.0 | Systematic Assessment |
| |
| COVID-19 | Infections and infestations | 24.0 | Systematic Assessment |
| |
| Upper respiratory tract infection | Infections and infestations | 24.0 | Systematic Assessment |
| |
| Gastroenteritis | Infections and infestations | 24.0 | Systematic Assessment |
| |
| Diarrhoea | Gastrointestinal disorders | 24.0 | Systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | 24.0 | Systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | 24.0 | Systematic Assessment |
| |
| Pruritus | Skin and subcutaneous tissue disorders | 24.0 | Systematic Assessment |
| |
| Erythema | Skin and subcutaneous tissue disorders | 24.0 | Systematic Assessment |
| |
| Oropharyngeal pain | Respiratory, thoracic and mediastinal disorders | 24.0 | Systematic Assessment |
| |
| Rhinitis allergic | Respiratory, thoracic and mediastinal disorders | 24.0 | Systematic Assessment |
| |
| Nasal congestion | Respiratory, thoracic and mediastinal disorders | 24.0 | Systematic Assessment |
| |
| Muscle rupture | Injury, poisoning and procedural complications | 24.0 | Systematic Assessment |
| |
| Anaemia | Blood and lymphatic system disorders | 24.0 | Systematic Assessment |
| |
| Lymphopenia | Blood and lymphatic system disorders | 24.0 | Systematic Assessment |
|
Not provided
Not provided
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Clinical Trial Information | CureVac AG | 0049 6976805870 | clinicaltrials@curevac.com |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Feb 18, 2022 | Oct 3, 2022 | SAP_001.pdf |
| ID | Term |
|---|---|
| D018352 | Coronavirus Infections |
| D000086382 | COVID-19 |
| D045169 | Severe Acute Respiratory Syndrome |
| ID | Term |
|---|---|
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D007239 | Infections |
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| C000722934 | CVnCoV COVID-19 vaccine |
| D022362 | Hepatitis A Vaccines |
| D022242 | Pneumococcal Vaccines |
| ID | Term |
|---|---|
| D014761 | Viral Hepatitis Vaccines |
| D014765 | Viral Vaccines |
| D014612 | Vaccines |
| D001688 | Biological Products |
| D045424 | Complex Mixtures |
| D022541 | Streptococcal Vaccines |
| D001428 | Bacterial Vaccines |
Not provided
Not provided
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Black or African American |
|
| Asian |
|
| Other |
|
|
| Dose 1: Any solicited systemic AEs |
|
|
| Dose 1: Any related solicited systemic AEs |
|
|
| Dose 2: Any solicited local AEs |
|
|
| Dose 2: Any solicited systemic AEs |
|
|
| Dose 2: Any related solicited systemic AEs |
|
|
| OG002 | CVnCoV 12 μg: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Active Control - Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Active Control - Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| OG002 | CVnCoV 12 μg: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| OG002 |
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| OG002 |
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
|
|
| CVnCoV 12 μg: Aged 18-60 Years |
Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were between the ages of 18 to 60 years old. CVnCoV was administered again as a booster vaccination on Day 180 in a sub-group of participants in Part 1. |
| OG003 | CVnCoV 12 μg: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. CVnCoV was administered again as a booster vaccination on Day 57 or Day 180 in a sub-group of participants in Part 1. |
| OG004 | Active Control - Hepatitis A Vaccine: Aged 18-60 Years | Participants in Part 1 and Part 2 were vaccinated with a hepatitis A vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged between 18 and 60 years old. |
| OG005 | Active Control - Pneumococcal Vaccine: Aged >60 Years | Participants in Part 1 and Part 2 were vaccinated with a pneumococcal vaccine as an intramuscular injection by needle in the deltoid area on Day 1 and Day 29. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 and Part 2 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 and Part 2 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 and Part 2 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 and Part 2 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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Participants in Part 1 and Part 2 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were between the ages of 18 to 60 years old. |
| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 and Part 2 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| OG002 | CVnCoV 12 μg: Aged >60 Years - Day 180 Booster | Participants in Part 1 were administered a booster vaccination with CVnCoV 12 μg as an intramuscular injection by needle in the deltoid area on Day 180. Participants in this group were aged over 60 years old. |
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| Grade 2 |
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| Grade 3 |
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| Moderate |
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| Severe |
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| Grade 2 |
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| Grade 3 |
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