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Safety and Immunogenicity Study of Revaccination With SCB-1019T in Healthy Adults
A Phase 1, Placebo-controlled, Randomized, Observer-blind Study to Describe the Safety, Tolerability and Immunogenicity of SCB-1019T in Adults Who Were Vaccinated With AREXVY at Least 18 Months Before
Who can join
Ages 60 to 85 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: 1. Male and female participants 60-85 years of age at the screening visit and who received AREXVY before. 2. Individuals are willing and able to comply with study requirements, including all scheduled visits, vaccination, laboratory tests, and other study procedures. 3. Individuals willing and able to give an informed consent, prior to screening. 4. Healthy participants as determined by medical history, physical examination, and clinical judgment of the investigator; participants with pre-existing stable medical conditions can be included (a stable medical condition is defined as a disease not requiring significant change in therapy or hospitalization for worsening disease during the 3 months before enrollment). Please refer to Protocol for full list of Inclusion and Exclusion criteria. Exclusion Criteria: 1. Acute disease or fever (≥38°C) at time of vaccination. Participants with a minor illness (mild diarrhea, mild upper respiratory infection) without fever may be enrolled at the discretion of the investigator. For participants with minor illness and/or fever at the time of vaccination, Visit 1 may be rescheduled within the allowed time-window. 2. Recurrent or un-controlled neurological disorders or seizures. 3. Serious or unstable chronic illnesses 4. Any history of dementia or any medical condition that moderately or severely impairs cognition 5. History of a severe adverse reaction associated with a vaccine or severe allergic reaction (e.g., anaphylaxis) to any component of the study vaccines. Please refer to Protocol for full list of Inclusion and Exclusion criteria.
About the study
CLO-SCB-1019-002 is the first study of SCB-1019T vaccine for revaccination in older adults who were previously vaccinated with AREXVY. The safety, tolerability and immunogenicity of SCB-1019T are assessed.
What is being tested
- Candidate vaccine, SCB-1019T (biological)
- AREXVY (biological)
- placebo (other)
Sponsor: Clover Biopharmaceuticals USA, LLC · Participants: 160 · Started: Mar 21, 2025
Contact the study team
- Xuesong Pei, MD · Phone: (+86) 18515445890
Official record on ClinicalTrials.gov — NCT06843317
Locations in the U.S.
| Arizona | AMR Phoenix, Phoenix |
| Florida | AMR Fort Myers, Fort Myers |
| Kentucky | AMR Lexington, Lexington |
| Missouri | AMR Kansas City, Kansas City |
| Tennessee | Knoxville, Knoxville |
Conditions
From ClinicalTrials.gov, data retrieved Oct 3, 2026. Each study sets its own eligibility; the study team decides who can join.