A Study of Safety and Immune Response to Different Doses of a Cytomegalovirus Vaccine in Healthy Adults

Completed · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Cytomegalovirus Infections

In brief

The purpose of this study is to assess the safety, reactogenicity and immune response of the candidate CMV recombinant protein subunit (CMVsu) vaccine consisting of a combination of glycoproteins B (gB) and pentamer antigens adjuvanted, regardless of baseline CMV sero-status. This FTiH study is conducted in healthy adults 18 to 50 years of age, in which the 4 dose levels of the vaccine are administered in a step-wise dose escalation manner, based upon safety adjudication.

Key facts

Study ID

NCT05089630

Run by

GlaxoSmithKline

People needed

333

Starts

2021-10-14

Expected to finish

2025-04-02

Last updated by the study team

2026-07-17

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Participants who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
• Written informed consent obtained from the participant prior to performance of any study specific procedure.
• A healthy adult (woman or man), 18 to 50 years of age at the time of the first study intervention administration.
• Healthy participants as established by medical history and clinical examination before entering the study.
• Participants who are women of non-childbearing potential may be enrolled in the study.
• Participants who are women of child-bearing potential may be enrolled in the study, if the participant:
• has practiced adequate contraception for 30 days prior to study intervention administration, and
• has a negative pregnancy test on the day of study intervention administration and
• has agreed to continue adequate contraception during the entire treatment period and for 3 months after completion of the study intervention administration series.
• Participants who agree to take appropriate infection control measures to prevent becoming infected with SARS-CoV2 during the study.
• Participants who initially fail screening due to COVID-19 infection may be re-screened and included in the study, within the screening window period.
• Participants with signs/symptoms suggestive of active COVID-19 (i.e., fever, cough, etc.) should be isolated for the time period recommended by CDC since the signs/symptoms started, and symptoms have resolved.
• Participants with known COVID-19 positive contacts should be quarantined for the time period since exposure recommended by CDC since the exposure and the participant remains symptom free or COVID test negative.
• Participants who are diagnosed with COVID-19 may receive their subsequent CMVsu vaccination dose provided they have no fever, and their condition is considered stable by the investigator (e.g., there may be mild lingering cough, but no shortness of breath or difficulty breathing) within the original schedule.
• Participants who initially fail screening due to other active infections may be re screened within the screening window period and included in the study, if they no longer have signs or symptoms of active infection in the judgment of the site investigator.
• If a participant has equivocal results on CMV serodiagnostic screening test, they are permitted to be re-screened if within the 60-day screening window. Flexibility in safety blood evaluations will be permitted within the Schedule of activities time intervals.

You may not qualify if…

• Medical conditions
• Known documented medical history of or viral hepatitis B or C infection.
• History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s).
• Any confirmed or suspected immunosuppressive or immunodeficient condition.
• Family history of congenital or hereditary immunodeficiency.
• History of or current autoimmune disease.
• Lymphoproliferative disorder or malignancy within previous 5 years (excluding effectively treated non-melanotic skin cancer).
• Hypersensitivity to latex.
• Major congenital defects
• Acute or chronic clinically significant pulmonary, cardiovascular, hepatic or renal functional abnormality.
• Recurrent history or uncontrolled neurological disorders.
• Any hematological or biochemical abnormality.
• Any acute or chronic, clinically significant disease or pulmonary, cardiovascular, hepatic, or renal functional abnormalities.
• Any medical condition that in the judgment of the investigator would make intramuscular injection unsafe.
• Participants with symptoms suggestive of active COVID-19 infection are excluded.
• Participants with known COVID-19 positive contacts within the past 14 days should be excluded for at least 14 days since the exposure and the participant remains symptom free.
• Any other clinical condition that, might pose additional risk to the participant due to participation in the study.
• Prior/Concomitant therapy
• Any history of or planned receipt of a CMV vaccine other than the study intervention at any time point.
• Use of other investigational/non-registered product during the period beginning 30 days before the first dose, or their planned use during the study period.
• Planned administration of any vaccine not foreseen by the study protocol 30 days before and 30 days after each study vaccination administration any licensed influenza vaccine administered > 15 days before/ after vaccination.
• In case of extraordinary emergency mass vaccination for an unforeseen public health threat the time period can be reduced if necessary, for that mass vaccination vaccine, which may be under emergency use authorization.
• COVID-19 vaccines should be given at least 30 days before or after administration of a GSK study vaccine. This interval can be reduced to > 14 days, if emergency vaccination is recommended by public health authorities.
• Candidate COVID-19 vaccines are not allowed.
• Chronic administration of immunosuppressants or other immune-modifying drugs within 3 months prior to the vaccine dose. Inhaled and topical steroids are allowed.

Where it is running

• GSK Investigational Site — Anaheim, California, United States
• GSK Investigational Site — Long Beach, California, United States
• GSK Investigational Site — Los Angeles, California, United States
• GSK Investigational Site — Hallandale, Florida, United States
• GSK Investigational Site — Miami, Florida, United States
• GSK Investigational Site — Lexington, Kentucky, United States
• GSK Investigational Site — Dearborn, Michigan, United States
• GSK Investigational Site — Springfield, Missouri, United States
• GSK Investigational Site — Lincoln, Nebraska, United States
• GSK Investigational Site — Omaha, Nebraska, United States
• GSK Investigational Site — Las Vegas, Nevada, United States
• GSK Investigational Site — Newark, New Jersey, United States
• GSK Investigational Site — Secaucus, New Jersey, United States
• GSK Investigational Site — New York, New York, United States
• GSK Investigational Site — Austin, Texas, United States
• GSK Investigational Site — Cedar Park, Texas, United States
• GSK Investigational Site — Galveston, Texas, United States
• GSK Investigational Site — Puyallup, Washington, United States

Full record on ClinicalTrials.gov

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