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NCT Number: NCT06843317

Safety and Immunogenicity Study of Revaccination With SCB-1019T in Healthy Adults

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.

Recruiting

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Key information

Age range

60 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

AMR Phoenix, Phoenix, Arizona, United States

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About this study

The study design will compare heterologous revaccination with SCB-1019T, homologous revaccination with AREXVY, or placebo in adults who were previously vaccinated with AREXVY. The sample size for this study is not based on formal statistical hypothesis testing but is acceptable for safety and immunogenicity evaluation in a phase 1 study. The study will be overseen by a safety monitoring committee.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female participants 60-85 years of age at the screening visit and who received AREXVY before.
  • Individuals are willing and able to comply with study requirements, including all scheduled visits, vaccination, laboratory tests, and other study procedures.
  • Individuals willing and able to give an informed consent, prior to screening.
  • 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

  • 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.
  • Recurrent or un-controlled neurological disorders or seizures.
  • Serious or unstable chronic illnesses
  • Any history of dementia or any medical condition that moderately or severely impairs cognition
  • 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.

Treatment and study plan

candidate vaccine, SCB-1019T

Biological

SCB-1019T is a novel bivalent recombinant RSV vaccine (CHO Cell) designed to broadly neutralize the two dominant circulating strains of the virus. The SCB-1019T vaccine consists of the PreF protein subunits from the two dominant circulating strains, strain A and strain B, fused to Trimer-Tag™.

AREXVY

Biological

positive comparator

Placebo

Other

Placebo Comparator

Primary outcomes

  1. To evaluate the safety and reactogenicity of revaccination with SCB-1019T vaccine

    Time frame: Within 7 days after vaccination

    Proportion of participants with local and systemic solicited AEs

  2. To evaluate the safety and reactogenicity of revaccination with SCB-1019T vaccine

    Time frame: Within 28 days after vaccination

    Proportion of participants with unsolicited AEs

  3. To evaluate the safety and reactogenicity of revaccination with SCB-1019T vaccine

    Time frame: Throughout the study period, from enrollment to 6 months follow up

    Proportion of participants with SAEs, AESIs, MAAEs, AEs leading to early termination from the study

Study contacts

Contact information is provided by the study sponsor or research team.

Xuesong Pei, MD

CONTACT

[email protected]

(+86) 18515445890

Sponsors and collaborators

Lead sponsor

Clover Biopharmaceuticals USA, LLC

Industry

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 24, 2025
Registry last updated
May 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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