Safety, Reactogenicity, and Immunogenicity Trial of CV2CoV mRNA Vaccine Against SARS-CoV-2 in Seropositive Adult Participants
- Conditions
- COVID-19SARS-CoV-2
- Interventions
- Biological: CV2CoV (2 µg)Biological: CV2CoV (8 µg)Biological: CV2CoV (20 µg)Biological: CV2CoV (4 µg)Biological: CV2CoV (12 µg)Biological: CV2CoV (16 µg)
- Registration Number
- NCT05260437
- Lead Sponsor
- GlaxoSmithKline
- Brief Summary
Prevention of COVID-19 caused by SARS-CoV-2.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 99
- Must provide documented informed consent prior to any study procedures being performed.
- Is capable of understanding and agrees to comply with planned study procedures and to be available for all study visits, including being willing and able to use electronic devices during the study.
- Has received at least 2 doses of Pfizer-BioNTech (Comirnaty) or Moderna (Spikevax) mRNA COVID-19 vaccine with the last dose of vaccine received at least 6 months prior to Screening and has provided documentation of receiving the vaccination series.
- Negative for SARS-CoV-2 infection by RT-PCR test at Screening.
- Is a male or nonpregnant female 18 to <65 years of age (younger adult group) or ≥65 years of age (older adult group) at Screening.
- Has a body mass index of 18 to 34.9 kg/m^2, inclusive, at Screening.
- If the participant is a woman of child bearing potential the participant agrees to practice true abstinence or use at least 1 highly effective form of contraception for at least 30 days prior to study vaccination up to 3 months after study vaccination.
- Agrees to refrain from blood or plasma donation from Screening and throughout the end of the study.
- Is healthy or medically stable as determined by medical history, clinical laboratory tests, vital sign measurements, and physical examination findings, as determined by investigator judgment.
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Participant is female and has a positive serum pregnancy test result at Screening or plans to become pregnant during the study.
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Participant is female and is breastfeeding or plans to breastfeed from study vaccination to 3 months after study vaccination.
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Has any clinically significant abnormal biochemistry or hematology finding (defined as ≥Grade 1) at Screening.
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Has any medical disease or condition that, in the opinion of the investigator, precludes study participation. This includes any acute, subacute, intermittent, or chronic medical disease or condition that would place the participant at an unacceptable risk of injury, render the participant unable to meet the requirements of the protocol, or may interfere with the evaluation of responses or the participant's successful completion of the trial.
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Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease or immunosuppressive/cytotoxic therapy.
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History of myocarditis, pericarditis, or idiopathic cardiomyopathy, or presence of any medical condition that increases risk of myocarditis or pericarditis, including cocaine abuse, cardiomyopathy, endomyocardial fibrosis, hypereosinophilic syndrome, hypersensitivity myocarditis, eosinophilic granulomatosis with polyangiitis, persistent myocardial viral infection (eg, due to enterovirus or adenovirus), and celiac disease.
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Has an acute febrile illness with a temperature ≥38.0°C or ≥100.4°F observed by the participant or at the study site within 72 hours prior to study vaccination. Participants with suspected COVID-19 symptoms should be excluded and referred for medical care.
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Has a prior confirmed diagnosis of chronic hepatitis B, hepatitis C, or HIV 1/2 infection or evidence of active infection at Screening.
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Has participated or plans to participate in another investigational study involving any investigational drug or device within 60 days or 5 half-lives, whichever is longer, before study vaccination and throughout the end of the study.
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Has previously participated in an investigational vaccine study with investigational vaccine administered within 6 months of study vaccination OR has received the last dose of >1 COVID-19 vaccine series (investigational and/or authorized) in the last 12 months.
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Has received or plans to receive any licensed vaccine within 4 weeks before or after study vaccination. Inactivated vaccines for influenza are permitted during the study if they are administered at least 14 days before or after study vaccination.
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Is planning to receive a COVID-19 booster vaccination for the duration of the study (for adults who are not covered by local recommendations to receive booster per current standard of care) or is planning to receive a COVID-19 booster vaccination on or before Day 29 of the study (for adults covered by local recommendations to receive booster).
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Has received or plans to receive immunoglobulins or any blood or blood products within 90 days before study vaccination and throughout the study.
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Has a history of hypersensitivity or severe allergic reaction, including anaphylaxis, generalized urticaria, angioedema, and other significant reactions to any previous vaccine or any component of the IP.
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Has a history of hypersensitivity or severe allergic reaction (including anaphylaxis, generalized urticaria, angioedema, and other significant reactions) to beta lactam antibiotics.
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Reports chronic use (more than 14 continuous days) of any medication that may be associated with changes in immune function including, but not limited to, systemic corticosteroids exceeding 10 mg/day of prednisone equivalent, allergy injections, immunoglobulins, interferons, immunomodulators, cytotoxic drugs, or other similar or toxic drugs within 6 months of study vaccination.
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Has a bleeding disorder or prior history of significant bleeding or bruising after IM injections or venipuncture.
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Has a history of alcohol abuse or other recreational drug use (excluding cannabis) within 6 months before study vaccination.
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Has any abnormal skin condition or permanent body art that would interfere with the ability to observe local reactions at the study vaccination injection site.
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Has had known close contact with anyone who had a confirmed SARS-CoV-2 infection within 14 days before study vaccination.
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Participant is an employee or family member of the investigator or study site personnel.
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Has any self-reported or medically-documented significant medical or psychiatric condition. Significant medical conditions include, but are not limited to, the following:
- Moderate or severe respiratory disease
- Uncontrolled hypertension, defined as an average systolic blood pressure ≥140 mmHg for participants ≤60 years old, and ≥150 mmHg for participants >60 years old, or a diastolic blood pressure ≥90 mmHg for any age
- Significant cardiovascular disease or history of myocarditis or pericarditis
- Neurological or neurodevelopmental conditions
- Ongoing malignancy or recent diagnosis of malignancy in the last 5 years (excluding basal cell and squamous cell carcinoma of the skin)
- Tuberculosis or nontuberculosis mycobacterial infection
- Autoimmune disease, including hypothyroidism without a defined nonautoimmune cause
- Immunodeficiency of any cause, including from solid organ transplant, blood or bone marrow transplant, use of corticosteroids, or use of other immune weakening medicines
- Type 1 or 2 diabetes mellitus regardless of disease control
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Has any of the following self-reported or medically-documented risk factors for severe COVID-19:
- Cancer
- Chronic kidney disease
- Sickle cell disease
- Cerebrovascular disease
- Cystic fibrosis
- Chronic liver disease
- Pulmonary fibrosis
- Thalassemia
- Smoking or other inhaled substance use, including tobacco, cannabis, or nicotine vapors, with an average of ≥5 cigarettes a day or equivalent (currently or within 1 year of Screening).
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Has a history of documented SARS-CoV-2 infection or COVID-19 within 6 months before Screening.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description CV2CoV Dose Cohort 1 (Group 1a 2μg) CV2CoV (2 µg) Participants received 2 μg CV2CoV intramuscularly. CV2CoV Dose Cohort 2 (8 μg) CV2CoV (8 µg) Participants received 8 μg CV2CoV intramuscularly. CV2CoV Dose Cohort 5 (20 μg) CV2CoV (20 µg) Participants were scheduled to receive 20 μg CV2CoV Intramuscularly, but there were no participants enrolled in this group, and hence, there was no vaccine administered in this study group. CV2CoV Dose Cohort 1 (Group 1b 4μg) CV2CoV (4 µg) Participants received 4 μg CV2CoV intramuscularly. CV2CoV Dose Cohort 3 (12 μg) CV2CoV (12 µg) Participants received 12 μg CV2CoV intramuscularly. CV2CoV Dose Cohort 4 (16 μg) CV2CoV (16 µg) Participants received 16 μg CV2CoV intramuscularly.
- Primary Outcome Measures
Name Time Method Number of Participants With Solicited Local Adverse Events (AEs) up to 7 Days After Study Vaccination From Day 1 to Day 7 (including Day 7) Assessed solicited local reactions were injection site pain, redness, swelling, and lymphadenopathy.
Number of Participants With Each Solicited Systemic AEs up to 7 Days After Study Vaccination From Day 1 to Day 7 (including Day 7) Assessed solicited systemic reactions were fever, headache, fatigue, myalgia, arthralgia, and chills.
Number of Participants With Unsolicited AEs up to 28 Days After Study Vaccination, Including Clinically Relevant Abnormal Clinical Safety Laboratory Findings From Day 1 to Day 28 (including Day 28) An unsolicited AE is defined as any AE that is volunteered from the participant and occurs within 28 days after vaccination.
Number of Participants With Medically Attended Adverse Events (MAAEs) From Study Vaccination Through the End of the Study From Day 1 up to Day 180 (including Day 180) An MAAE is defined as an AE that results in a visit to a medical professional. Medically attended visits are defined as a telemedicine visit, physician's office visit, urgent care visit, emergency room visit, hospitalization, or death.
Number of Participants With Adverse Events of Special Interest (AESIs) From Study Vaccination Through the End of the Study From Day 1 up to Day 180 (including Day 180) An AESI (serious or nonserious) is defined as an AE or SAE of scientific and medical concern specific to the sponsor's product or program, for which ongoing monitoring and rapid communication by the investigator to the sponsor could be appropriate.
Number of Participants With Serious Adverse Events (SAEs) From Study Vaccination Through the End of the Study From Day 1 up to Day 180 (including Day 180) An SAE is defined as any event that: • Results in death • Is immediately life-threatening • Requires inpatient hospitalization or prolongation of existing hospitalization • Results in persistent or significant disability/incapacity • Is a congenital anomaly/birth defect • Is a spontaneous miscarriage Important medical events that may not result in death, be life-threatening, or require hospitalization may be considered SAEs when, based upon appropriate medical judgment, they may jeopardize the participant or may require medical or surgical intervention to prevent one of the outcomes listed in this definition. Examples of such medical events include allergic bronchospasm requiring intensive treatment in an emergency room or at home, blood dyscrasias or convulsions that do not result in inpatient hospitalization, or the development of drug dependency or drug abuse.
- Secondary Outcome Measures
Name Time Method GMI From Baseline of Binding IgG Against SARS CoV-2 S Protein and RBD At Day 8, Day 15, Day 29, Day 85, and Day 180 Geometric Mean Titers (GMTs) of Neutralizing Antibody Titers Against Pseudovirus Bearing Spike Protein From SARS CoV 2 Wild Type (WT) At Day 1, Day 8, Day 15, Day 29, Day 85, and Day 180 GMTs of Binding Immunoglobulin G (IgG) Against SARS CoV-2 S Protein and Receptor-Binding Domain (RBD) At Day 8, Day 15, Day 29, Day 85 and Day 180 Percentage of Participants With Seroresponse (>= 4 Fold Rise From Baseline) at Day 29 After the Booster Dose At Day 29 (29 days post booster dose) Percentage of participants with seroresponse against antigen SARS-CoV-2 WT, Beta, Omicron BA.1, Omicron BA.2, Delta assessed were reported. Seroresponse was defined as greater than equal to (\>=) 4-fold increase from Day 1 (Baseline) to the Day 29. The fold rise was calculated as the ratio of the post-vaccination Neutralizing Antibody Titers to the pre-vaccination Neutralizing Antibody Titers.
Geometric Mean Increase (GMI) From Baseline of Neutralizing Antibody Titers Against Pseudovirus Bearing Spike Protein From SARS CoV 2 WT at Each Collection Time Point At Day 8, Day 15, Day 29, Day 85, and Day 180
Trial Locations
- Locations (12)
GSK Investigational Site
🇺🇸West Jordan, Utah, United States
Accel Research Sites
🇺🇸Lakeland, Florida, United States
MD Clinical - Velocity
🇺🇸Hallandale Beach, Florida, United States
Suncoast Research Group LLC - ERN-PPDS
🇺🇸Miami, Florida, United States
Affinity Health Corp
🇺🇸Oak Brook, Illinois, United States
Lynn Institute of Norman - ERN - PPDS
🇺🇸Norman, Oklahoma, United States
Velocity Clinical Research - Cleveland
🇺🇸Cleveland, Ohio, United States
DM Clinical - Cyfair Clinical Research Center
🇺🇸Tomball, Texas, United States
Research Your Health - Elite
🇺🇸Plano, Texas, United States
Velocity Clinical Research - Salt Lake City - Jordan Valley-ERN-PPDS
🇺🇸West Jordan, Utah, United States
Lynn Health Science Institute
🇺🇸Oklahoma City, Oklahoma, United States
Lynn Institute of Denver - ERN
🇺🇸Aurora, Colorado, United States