Immunogenicity and Safety of V503 in Chinese Males 9 Through 19 Years Old (V503-053)
- Summary
- This study is designed to demonstrate non-inferior immunogenicity of 3 doses of the 9-Valent Human Papillomavirus (9vHPV) vaccine (GARDASIL™9, V503) in Chinese males 9 through 19 years of age, and 2 doses of the 9vHPV vaccine in Chinese males 9 through 14 years of age, compared to the 3 dose regimen in Chinese males 20 through 26 years of age (from Merck Protocol V503-052). The primary hypothesis is that each of the 3-dose regimen in Chinese males aged 9 through 19 years and 2-dose regimens in Chinese males aged 9 through 14 years induces non-inferior competitive Luminex immunoassay (cLIA) geometric mean titers (GMTs) at one month post last dose compared to the 3-dose regimen in Chinese adult males aged 20 through 26 years. A noninferiority margin of 0.67 in the GMT ratio (9 through 19 years of age or 9 through 14 years of age vs 20 through 26 years of age) is used for each HPV type.
- Short title
- Immunogenicity and Safety of V503 in Chinese Males 9 Through 19 Years Old (V503-053)
- Official title
- A Phase 3 Open-Label Immunogenicity and Safety Study of 2-Dose Regimens of V503, a 9-Valent Human Papillomavirus (HPV) Vaccine in Chinese Males 9 Through 14 Years Old and 3-Dose Regimen of V503 in Chinese Males 9 Through 19 Years Old
- Control arm
- Open label
- Registry reports results
- Listing at source
- Listed
- Recruitment status
- Active, not recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Completion date
- 2029-02-19
- First posted
- 2022-04-06
- Registry last updated
- 2023-01-19
- Primary completion date
- 2029-02-19
- Start date
- 2022-05-07
- Participants
- 1,590
- Participant count basis
- Estimated
- Planned participants
- 1,590
- Protocol amendments
- Number of sites
- Data monitoring committee
- Registry sponsor category
- Industry
- Lead sponsor
- Merck Sharp & Dohme LLC
- Source registry
- ClinicalTrials.gov
- Registry ID
- NCT05314023
- ClinicalTrials.gov ID
- NCT05314023
- Registry record
- Open registry record
- Allocation
- Not randomised
- Model
- Parallel groups
- Purpose
- Prevention
- Masking
- No masking
Competitive Luminex immunoassay (cLIA) GMTs to 9 vaccine types of 9vHPV vaccine at one month post last dose
Timeframe: Up to Month 13
cLIA GMT to each of 9 vaccine types of 9vHPV vaccine at one month post last dose. The GMT for each HPV type will be reported in mMU/mL.
cLIA GMTs to 9 vaccine types of 9vHPV vaccine up to 60 months post last dose
Timeframe: Up to 72 months
cLIA GMT to each of 9 vaccine types of 9vHPV vaccine at up to 60 months post last dose. The GMT for each HPV type will be reported in mMU/mL.
cLIA seropositivity percentages to 9 vaccine types of 9vHPV vaccine
Timeframe: Up to 72 months
cLIA seropositivity to each of 9 vaccine types of 9vHPV vaccine. The percentage of participants who are seropositive for each HPV type will be summarized.
cLIA seroconversion percentages to 9 vaccine types of 9vHPV vaccine
Timeframe: Up to Month 13
cLIA seroconversion to each of 9 vaccine types of 9vHPV vaccine. The percentage of participants who are seropositive for each HPV type will be summarized.
Immunoglobulin G Luminex immunoassay (IgG LIA) GMTs to 9 vaccine types of 9vHPV vaccine at one month post last dose
Timeframe: Up to Month 13
IgG LIA GMT to each of 9 vaccine types of 9vHPV vaccine at one month post last dose. The GMT for each HPV type will be reported in mMU/mL.
IgG LIA seroconversion percentages to 9 vaccine types of 9vHPV vaccine
Timeframe: Up to Month 13
IgG LIA seroconversion to each of 9 vaccine types of 9vHPV vaccine. The percentage of participants who are seropositive for each HPV type will be summarized.
Percentage of participants experiencing solicited injection-site adverse events (AEs),
Timeframe: Day 1 through Day 8 following any study vaccination
An AE is any untoward medical occurrence in a participant which does not necessarily have a causal relationship with study vaccine. An AE can therefore be any unfavorable and unintended sign, symptom, or disease temporally associated with the use of study vaccine or a protocol-specified procedure, whether or not considered related to the study vaccine or protocol-specified procedure. Solicited injection-site AEs such as erythema, swelling, pain, and induration at the injection site will be recorded.
Percentage of participants experiencing solicited systemic AEs
Timeframe: Day 1 through Day 8 following any study vaccination
An AE is any untoward medical occurrence in a participant which does not necessarily have a causal relationship with study vaccine. An AE can therefore be any unfavorable and unintended sign, symptom, or disease temporally associated with the use of study vaccine or a protocol-specified procedure, whether or not considered related to the study vaccine or protocol-specified procedure. Systemic AEs are those not categorized as injection-site AEs.
Percentage of participants experiencing serious AEs (SAEs)
Timeframe: Up to 72 months
A SAE is an AE that results in death, is life threatening, results in a persistent or significant disability or incapacity, results in or prolongs an existing hospitalization, is a congenital anomaly or birth defect, or is another important medical event.
IgG LIA GMTs to 9 vaccine types of 9vHPV vaccine up to 60 months post last dose
Timeframe: Up to 72 months
IgG LIA GMT to each of 9 vaccine types of 9vHPV vaccine up to 60 months post last dose. The GMT for each HPV type will be reported in mMU/mL.
IgG LIA seropositivity percentages to 9 vaccine types of 9vHPV vaccine
Timeframe: Up to 72 months
IgG LIA seropositivity to each of 9 vaccine types of 9vHPV vaccine. The percentage of participants who are seropositive for each HPV type will be summarized.
- Sex
- Male
- Age groups
- Children, Adults
- Minimum age
- 9 Years
- Maximum age
- 19 Years
- Healthy volunteers
- Yes
- Is a healthy Chinese male.
- Has not had sexual debut at the time of enrollment, and does not plan on becoming sexually active during the vaccination period (Day 1 through one month post last dose).
- Has a history of known prior vaccination with an HPV vaccine.
- Has a history of HPV-related external genital lesions, HPV-related intra-anal lesions, or HPV-related head and neck cancer.
- Has a history of severe allergic reaction that required medical intervention.
- Has received immune globulin or blood-derived products in the past 6 months or plans to receive any before one month post last dose.
- Has a history of splenectomy, is currently immunocompromised, or has been diagnosed with immunodeficiency, human immunodeficiency virus (HIV), lymphoma, leukemia, systemic lupus erythematosus, rheumatoid arthritis, juvenile rheumatoid arthritis, inflammatory bowel disease, or other autoimmune condition.
- Has received immunosuppressive therapy in the past year, excluding inhaled, nasal, or topical corticosteroids and certain regimens of systemic corticosteroids.
- Has a known thrombocytopenia or coagulation disorder that would contraindicate IM injections.
- Liucheng County Centers for Disease Control and Prevention ( Site 0005)Liuzhou, China
- Center for Disease Control and Prevention of Rong An ( Site 0006)Liuzhou, China
- Loudi Public Health Hospital (Loudi Occupational Disease Prevention And Treatment Hospital) ( Site 0Louxing District, China
- Yuechi Disease Prevention and Control Center ( Site 0002)Guang’an, China
- Santai County Center for Disease Control and Prevention ( Site 0001)Mianyang, China
Other registry identifiers
- V503-053