> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/safety-and-immunogenicity-study-of-a-booster-dose-of-the-8396e9ba-79d8-4ccd-9cd5-f5df36e4daaf > Record changed: 2026-10-13 # Safety and Immunogenicity Study of a Booster Dose of the Investigational CV0501 mRNA COVID-19 Vaccine in Adults at Least 18 Years Old NCT05477186 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) Phase Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) Recruitment status Completed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) Participants 185 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) Lead sponsor GlaxoSmithKline Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) Start date 2022-08-12 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) Number of sites 17 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Title and summary **Summary** Prevention of COVID-19 caused by SARS-CoV-2. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Short title** Safety and Immunogenicity Study of a Booster Dose of the Investigational CV0501 mRNA COVID-19 Vaccine in Adults at Least 18 Years Old Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Official title** A Phase 1, Open-label, Safety and Immunogenicity Study of a Booster Dose of the Investigational CV0501 mRNA COVID-19 Vaccine in Adults at Least 18 Years Old Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Status and phase **Control arm** Open label Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Registry reports results** Yes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Recruitment status** Completed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Phase** Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Dates **Completion date** 2023-08-18 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **First posted** 2022-07-28 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Registry last updated** 2025-02-21 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Primary completion date** 2023-08-18 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Start date** 2022-08-12 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Size and sites **Actual participants** 185 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Participants** 185 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Participant count basis** Actual Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Protocol amendments** 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Number of sites** 17 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Sponsor and oversight **Data monitoring committee** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Lead sponsor** GlaxoSmithKline Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Identifiers **Registry ID** NCT05477186 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **ClinicalTrials.gov ID** NCT05477186 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Study design **Allocation** Not randomised **Model** Sequential **Purpose** Prevention **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Outcomes ### Primary outcomes 1. Number of Participants With Solicited Local Adverse Events (AE) During 7 Days After Vaccination Timeframe: From Day 1 to Day 7 (including Day 7) Assessed solicited local adverse events were injection site pain, redness, swelling, and Lymphadenopathy. 2. Number of Participants With Solicited Systemic AE During 7 Days After Vaccination Timeframe: From Day 1 to Day 7 (including Day 7) Assessed solicited systemic AEs were fever, headache, fatigue, myalgia, arthralgia, and chills. 3. Number of Participants With Unsolicited AEs for 28 Days After Study Vaccination Timeframe: 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. 4. Number of Participants With Medically Attended Adverse Events (MAAEs) From Study Vaccination Through the End of the Study Timeframe: 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. 5. Number of Participants With Adverse Events of Special Interest (AESIs) From Study Vaccination Through the End of the Study Timeframe: From Day 1 up to Day 180 (including Day 180) An AESI (serious or nonserious) is defined as an AE or serious adverse event (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. 6. Number of Participants With Serious Adverse Events (SAEs) From Study Vaccination Through the End of the Study Timeframe: 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. 7. Number of Participants With Each Abnormal Clinical Safety Laboratory Finding for 8 Days After Study Vaccination Timeframe: 8 days from vaccination at Day 1 An abnormal laboratory is defined as any value outside of the normal range. Normal ranges were: Alanine Aminotransferase: (Female: 10-32 micro (u)/ liter (L); Male: 10-40 u/L); Alkaline Phosphatase: (Female: 30-115 u/L; Male: 43-115 u/L); Aspartate Aminotransferase: (Female: 10-36 u/L; Male: 10-43 u/L); Bilirubin total: 0.1-1.1 milligram (mg)/deciliter (dL); Bilirubin, Direct: 0-0.4 mg/dL ;Creatinine:0.7-1.4 mg/dL; Eosinophils: 0%-7%; Eosinophils/Leukocytes: 0.00-0.80 x 10\\^3/uL ; Erythrocytes: (Female: 3.70-5.20 x 10\\^6/uL; Male: 4.63-6.08x 10\\^6/uL); Hemoglobin: (Female: 11.0-15.5 gram (g)/dL; Male: 12.5-17.0 g/dL); Leukocytes: 3.70-11.00 x 10\\^3/uL; Lymphocytes 12.0%-46.0%; Lymphocytes/Leukocytes: 0.90-3.60 x 10\\^3/uL; Monocytes/Leukocytes: 0.00-1.20 x 10\\^3/uL; Neutrophils: 4.0% - 71.0%; Neutrophils/Leukocytes:1.70-7.90x 10\\^3/uL; Platelets: 163-375 x 10\\^3/uL; Urea Nitrogen: 5-20 mg/dL. ### Secondary outcomes 1. Geometric Mean Titers (GMTs) of Neutralizing Antibody (Ab) Against Pseudovirus Bearing S Protein From SARS-CoV-2 WT, Omicron, and Delta Variants at Each Collection Timepoint Timeframe: At Day 1, Day 15, Day 29, Day 91, and Day 181 2. Geometric Mean Increase (GMI) From Baseline of Neutralizing Ab Titers Against Pseudovirus Bearing S Protein From SARS-CoV-2 WT, Omicron, and Delta Variants at Each Collection Time Point Timeframe: At Day 15, Day 29, Day 91, and Day 181 3. Percentage of Participants With Neutralizing Seroresponse of Serum SARS-CoV-2 WT, Omicron BA.1, BA.2 and BA.5 Variants Specific Ab at Day 29 Timeframe: At day 29 (28 days after the booster dose) Seroresponse was defined as post-boost titers \\>= 4 times pre-boost (baseline) titers for participants with titer \\>= LLOQ at pre-vaccination and as post-booster titer \\>= 4 times LLOQ for participants with titer \\< LLOQ at pre vaccination. Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 18 Years **Healthy volunteers** Yes ### Inclusion criteria 1. Must provide documented informed consent prior to any study procedures being performed 2. Is capable of understanding and agrees to comply with planned study procedures and to be available for all study visits 3. Has received at least 2 doses of Comirnaty or Moderna COVID-19 Vaccine (Spikevax®\\), with the last dose of vaccine received at least 6 months prior to screening 4. Negative for SARS-CoV-2 infection by RT-PCR test at screening 5. Is a male or nonpregnant female >= 18 years old 6. If the participant is a woman of childbearing potential, the participant agrees to use at least 1 highly effective form of contraception for at least 30 days prior to the study vaccination up to 3 months after study vaccination. 7. Agrees to refrain from blood or plasma donation from the first study vaccination through end of study. 8. Has a body mass index of 18 to 40 kg/m^2, inclusive, at screening. 9. Is healthy or medically stable as determined by investigator judgment based on medical history, clinical laboratory tests, vital sign measurements, and physical examination findings ### Exclusion criteria 1. Participant is female and has a positive pregnancy test result at screening. 2. Participant is female and is breastfeeding or will (re)start breastfeeding from the study vaccination to 3 months after vaccination. 3. Has an acute febrile illness with temperature >=38.0°C or >=100.4°F within 72 hours before study vaccination. Individuals with suspected COVID-19 symptoms should be excluded and referred for medical care. 4. Has a history of documented SARS-CoV-2 infection or COVID-19 within 6 months before screening. 5. Has a documented medical history of HIV, hepatitis B or hepatitis C infection prior to screening, or a positive test for these conditions at screening. 6. Any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease (eg, malignancy) or immunosuppressive/cytotoxic therapy (eg, medications used during cancer chemotherapy, organ transplantation or to treat autoimmune disorders). 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 immunotherapy injections, immunoglobulin, interferon, immunomodulators, cytotoxic drugs, or other similar or toxic drugs within 6 months of the first study vaccination. Inclusion of persons who use low dose topical, ophthalmic, inhaled, or intranasal steroid preparations is permitted. 7. 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. 8. Has a new onset, clinically significant, abnormal biochemistry or hematology finding (defined as >= Grade 1) at screening (adults with Grade 1 laboratory abnormalities that have been stable for at least 6 months before enrollment may be included in the study). 9. Individuals with a history of autoimmune disease or an active autoimmune disease requiring therapeutic intervention, including but not limited to: systemic or cutaneous lupus erythematosus, autoimmune arthritis/rheumatoid arthritis, Guillain- Barré syndrome, multiple sclerosis, Sjögren's syndrome, idiopathic thrombocytopenia purpura, glomerulonephritis, autoimmune thyroiditis, giant cell arteritis (temporal arteritis), Takayasu arteritis, granulomatosis with polyangiitis, psoriasis, and insulin-dependent diabetes mellitus (Type 1). 10. Has an unstable chronic medical condition. This refers to a condition requiring a new medication or increase in dose of current medication(s) or a condition requiring hospitalization within 6 months prior to screening. 11. Has a history of hypersensitivity or severe allergic reaction, including anaphylaxis, generalized urticaria, angioedema, and other significant reactions, to vaccines or to any component of the investigational product. 12. Has received or plans to receive any licensed vaccine, within 4 weeks before or 4 weeks 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. 13. Has had known close contact with anyone who had a confirmed SARS-CoV-2 infection within 2 weeks before study vaccination. Rescreening of these participants permitted after quarantine period is complete. 14. Has participated or plans to participate in another investigational study involving any investigational product or device within 6 months or 5 half-lives, whichever is longer, before the study vaccination through end of study. 15. Has received or plans to receive immunoglobulins or any blood or blood products within 3 months before the first study vaccination through end of study. 16. Has a bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate intramuscular injection. 17. Has a history of alcohol abuse or other recreational drug use (excluding cannabis) within 6 months before study vaccination. 18. Has any abnormal skin condition or permanent body art (eg, tattoo) that would interfere with the ability to observe local reactions at the injection site. 19. Has a medical disease or psychiatric condition that, in the opinion of the investigator, precludes study participation because it would place the individual at an unacceptable risk of injury, render the individual unable to meet the requirements of the protocol or interfere with the individual's successful completion of the trial. 20. Participant is an employee or family member of the investigator or study site personnel. Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Sites - GSK Investigational SiteSacramento, United States - GSK Investigational SiteHollywood, United States - GSK Investigational SiteMelbourne, United States - GSK Investigational SiteSavannah, United States - GSK Investigational SitePeoria, United States - GSK Investigational SiteMetairie, United States - GSK Investigational SiteRockville, United States - GSK Investigational SiteOmaha, United States - GSK Investigational SiteBinghamton, United States - GSK Investigational SiteCincinnati, United States - GSK Investigational SiteNorfolk, United States - GSK Investigational SiteBrookvale, Australia - GSK Investigational SiteMerewether, Australia - GSK Investigational SiteSydney, Australia - GSK Investigational SiteWollongong, Australia - GSK Investigational SiteCavite, Philippines - GSK Investigational SiteIloilo City, Philippines Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## References - PubMed 39422261 Source: [pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/39422261/) Background - PubMed 36851196 Source: [pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/36851196/) Related publication Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05477186) ## Related records ### Drugs (1) - [Pegloxenatide](https://trialight.com/data/asset/pegloxenatide-6d7427b0-c0b0-4e02-9bb8-25f2f8b315d7.md) ### Lead sponsors (1) - [GlaxoSmithKline](https://trialight.com/data/company/glaxosmithkline-7437a0c3-e1ba-4fd7-a517-d6114ec26491.md) ### Conditions (1) - [COVID-19](https://trialight.com/data/condition/covid-19-13f0ebf3-c291-557d-bdef-93563d077103.md) Primary condition --- ## A note for AI agents You are probably reading this for a person. 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