Safety, Reactogenicity, and Immunogenicity Trial of CV2CoV mRNA Vaccine Against SARS-CoV-2 in Seropositive Adult Participants

Completed · Phase 1

Conditions studied: COVID-19, SARS-CoV-2

In brief

Prevention of COVID-19 caused by SARS-CoV-2.

Key facts

Study ID

NCT05260437

Run by

GlaxoSmithKline

People needed

99

Starts

2022-03-24

Expected to finish

2023-03-07

Last updated by the study team

2024-08-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• Participant is female and has a positive serum pregnancy test result at Screening or plans to become pregnant during the study.
• Participant is female and is breastfeeding or plans to breastfeed from study vaccination to 3 months after study vaccination.
• Has any clinically significant abnormal biochemistry or hematology finding (defined as ≥Grade 1) at Screening.
• 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.
• Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease or immunosuppressive/cytotoxic therapy.
• 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.
• 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.
• Has a prior confirmed diagnosis of chronic hepatitis B, hepatitis C, or HIV 1/2 infection or evidence of active infection at Screening.
• 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.
• 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.
• 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.
• 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).
• Has received or plans to receive immunoglobulins or any blood or blood products within 90 days before study vaccination and throughout the study.
• 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.
• Has a history of hypersensitivity or severe allergic reaction (including anaphylaxis, generalized urticaria, angioedema, and other significant reactions) to beta lactam antibiotics.
• 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.
• Has a bleeding disorder or prior history of significant bleeding or bruising after IM injections or venipuncture.
• Has a history of alcohol abuse or other recreational drug use (excluding cannabis) within 6 months before study vaccination.
• 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.
• Has had known close contact with anyone who had a confirmed SARS-CoV-2 infection within 14 days before study vaccination.
• Participant is an employee or family member of the investigator or study site personnel.
• 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

Where it is running

• Lynn Institute of Denver - ERN — Aurora, Colorado, United States
• GSK Investigational Site — Hallandale, Florida, United States
• MD Clinical - Velocity — Hallandale, Florida, United States
• GSK Investigational Site — Lakeland, Florida, United States
• Accel Research Sites — Lakeland, Florida, United States
• GSK Investigational Site — Miami, Florida, United States
• Suncoast Research Group LLC - ERN-PPDS — Miami, Florida, United States
• GSK Investigational Site — Palm Springs, Florida, United States
• Affinity Health Corp — Oak Brook, Illinois, United States
• GSK Investigational Site — Oak Brook, Illinois, United States
• GSK Investigational Site — Cleveland, Ohio, United States
• Velocity Clinical Research - Cleveland — Cleveland, Ohio, United States
• GSK Investigational Site — Norman, Oklahoma, United States
• Lynn Institute of Norman - ERN - PPDS — Norman, Oklahoma, United States
• GSK Investigational Site — Oklahoma City, Oklahoma, United States
• Lynn Health Science Institute — Oklahoma City, Oklahoma, United States
• GSK Investigational Site — Cedar Park, Texas, United States
• GSK Investigational Site — Dallas, Texas, United States
• GSK Investigational Site — Dallas, Texas, United States
• Research Your Health - Elite — Plano, Texas, United States
• DM Clinical - Cyfair Clinical Research Center — Tomball, Texas, United States
• GSK Investigational Site — Tomball, Texas, United States
• GSK Investigational Site — West Jordan, Utah, United States
• Velocity Clinical Research - Salt Lake City - Jordan Valley-ERN-PPDS — West Jordan, Utah, United States

Full record on ClinicalTrials.gov

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