A Study to Evaluate the Immunogenicity and Safety of Nonavalent Human Papillomavirus (HPV) Vaccine

NCT ID: NCT06207175

Last Updated: 2024-01-23

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 1260 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-21
• Study Completion Date: 2026-01-25

Brief Summary

This Study to Evaluate the Immunogenicity and Safety of Candidate Recombinant Nonavalent (types 6/11/16/18/31/33/45/52/58) Human Papillomavirus (HPV) Vaccine (Escherichia coli) Administered Intramuscularly in Healthy Female Participants Aged 18 to 45 Years

Detailed Description

This is a randomized, observer blinded, active controlled, multicenter clinical study.

A total of approximately 1,260 healthy female participants aged 18 to 45 years old who meet eligibility will be enrolled, and be randomly assigned into 2 groups in a 1:1 ratio.

Immunogenicity: Blood samples (5.0 mL each time) will be collected for all participants prior to the 1st dose of vaccination and on 1, 6, 12, 18 months after full vaccination for anti-HPV type 6/11/16/18/31/33/45/52/58 neutralizing antibodies and Immunoglobulin G antibodies testing.

Safety evaluation (for all participants):To assess solicited (local and systemic) Adverse Event (AEs) within 7 days after each dose of vaccination, unsolicited Adverse Event (AEs) within 30 days after each dose of vaccination, and Serious Adverse Event (SAEs) from 1st dose to 18 months after full vaccination.

Collection of pregnancy events:To assess the occurrence of pregnancy events in all participants from 1st dose to 18 months after full vaccination. The subject will be followed to determine the outcome of the pregnancy.

At the end of the pregnancy, be it a full-term or premature birth, information on the status of the newborn(s) will be followed up during the first 12 months of life.

Conditions

Human Papillomavirus Infection

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Nonavalent HPV study vaccine

Study vaccine: Recombinant Nonavalent (types 6/11/16/18/31/33/45/52/58) Human Papillomavirus (HPV) Vaccine (Escherichia coli) (Hereinafter referred to as "Nonavalent HPV study vaccine")

Provided by: Beijing Health Guard Biotechnology, Inc.

Dosage: 0.5 mL per dose

Appearance: White, cloudy liquid suspension

Dosage form: 0.5-mL suspension for injection as a prefilled syringe

Route of administration: Intramuscular injection into the lateral deltoid muscle of the upper arm

Vaccination schedule in this study：3 injections on a 0, 2, 6-month schedule.

Group Type: EXPERIMENTAL

Nonavalent HPV study vaccine

Intervention Type: BIOLOGICAL

A 3-dose regimen administered at months 0, 2 and 6.

GARDASIL® 9

Control vaccine: GARDASIL® 9

Manufacturer: Merck Sharp and Dohme Corp (MSD).

Dosage: 0.5 mL per dose

Appearance: After thorough agitation, GARDASIL® 9 is a white cloudy liquid

Dosage form: 0.5-mL suspension for injection as a prefilled syringe

Route of administration: Intramuscular injection into the lateral deltoid muscle of the upper arm

Vaccination schedule：3 injections on a 0, 2, 6-month schedule.

Group Type: ACTIVE_COMPARATOR

GARDASIL® 9

Intervention Type: BIOLOGICAL

A 3-dose regimen administered at months 0, 2 and 6.

Interventions

Nonavalent HPV study vaccine

A 3-dose regimen administered at months 0, 2 and 6.

Intervention Type: BIOLOGICAL

GARDASIL® 9

A 3-dose regimen administered at months 0, 2 and 6.

Intervention Type: BIOLOGICAL

Other Intervention Names

Recombinant Nonavalent (types 6/11/16/18/31/33/45/52/58) Human Papillomavirus (HPV) Vaccine (Escherichia coli)

Eligibility Criteria

Inclusion Criteria

1. *Healthy female participants, aged between 18 years and 45 years as of the 1st dose of vaccination (18 years ≤ age < 46 years).

2. Prior to enrolment, written informed consent obtained from the participants.

3. *Participants must be either of non-childbearing potential, or if of childbearing potential, they must be abstinent or have practiced adequate contraception for 14 days prior to 1st vaccination, and agree to continue such precautions for 1 month after full vaccination.

[Effective contraception includes oral contraceptives, injectable or implantable contraception, extended-release topical contraceptives, hormonal patches, intrauterine devices (IUDs), sterilization, abstinence, condoms (for males), diaphragms, cervical caps, etc.]; Women of Childbearing Potential participants have a negative urine pregnancy test before the 1st dose.

4. Participants are able to comply with study protocol, including all scheduled visits, vaccinations, laboratory tests, and other study procedures.

Note: For items with an asterisk (*), If the subject does not meet the criteria, the visit may be rescheduled when the criteria are met.

Exclusion Criteria

1. * Participant has fever (axillary temperature ≥ 37.3℃) within 24 hours prior to the 1st dose of vaccination;

2. Participant has vaccinated previously or plans to vaccinate with other HPV vaccines during the study period;

3. Participant is participating or plans to participate in other clinical studies during the period of this study;

4. Participant has a history of a positive test for HPV, or a history of an abnormal Pap test result showing atypical squamous cells - undetermined significance (ASC-US), atypical squamous cells - cannot exclude HSIL (ASC-H), low-grade squamous intraepithelial lesion (LSIL), high-grade squamous intraepithelial lesion (HSIL), or atypical glandular cells. Participant has a history of an abnormal cervical biopsy result showing cervical intraepithelial neoplasia (CIN), adenocarcinoma in situ or cervical cancer;

5. Participant has a history of HPV-related genital diseases (e.g., genital warts, Vulvar Intraepithelial Neoplasia, Vaginal Intraepithelial Neoplasia, vulvar cancer, vaginal cancer or anal cancer), a history of venereal disease (e.g., syphilis, gonorrhea, genital chlamydial infection, genital herpes, chancroid, lymphogranuloma venereum, inguinal granuloma, etc.);

6. Participant has a history of allergy to any component of the study vaccine or severe allergic reaction to vaccine (including but not limited to anaphylaxis, allergic laryngeal edema, anaphylactic purpura, thrombocytopenic purpura, or localized allergic necrosis (Arthus reaction), severe urticaria, dyspnea, angioneurotic edema, etc.);

7. Immunocompromised participant or participant that has been diagnosed with congenital or acquired immunodeficiency, human immunodeficiency virus (HIV) infection, lymphoma, leukemia, systemic lupus erythematosus (SLE), rheumatoid arthritis, juvenile rheumatoid arthritis (JRA), inflammatory bowel disease, or other autoimmune condition;

8. Participant who has/had epilepsy, excluding a history of febrile seizures under 2 years of age, or alcoholic epilepsy within 3 years prior to alcohol withdrawal;

9. Participant who has severe liver and kidney disease, severe cardiovascular disease, severe diabetes, malignant tumors, severe infectious diseases (e.g., tuberculosis, chronic hepatitis B/C, syphilis, etc.), is unsuitable to participate in this study based on the investigator's judgement;

10. Participant who has thrombocytopenia or any coagulopathy that is not suitable for intramuscular injection;

11. Asplenia or functional asplenia, complete or partial splenectomy from any cause;

12. Participant who is receiving or has received prolonged use (>14 days) of immunosuppressive or other immunomodulatory drugs (e.g., corticosteroids, ≥20 mg/d prednisone or equivalent; however, topical medications such as ointments, eye drops, inhalants or nasal sprays are permitted) within 6 months prior to the 1st dose of vaccination, or plans to receive them during the period from 1st dose of vaccination to 30 days after full vaccination;

13. Participant has received immunoglobulin or other blood products within 3 months prior to the 1st dose of vaccination or plans to receive them during the period from the 1st dose of vaccination to 30 days after full vaccination;

14. *Participant who has acute illness or in acute exacerbation of chronic diseases or use antipyretic, analgesic and anti-allergic drugs (e.g., paracetamol, ibuprofen, aspirin, loratadine, cetirizine, etc.) within 3 days prior to vaccination;

15. *Participant who has vaccinated with inactivated/recombinant/nucleic acid vaccines (non-attenuated vaccines) within 14 days before enrollment or attenuated vaccines within 28 days before enrollment, or plans to administrate vaccine(s) from the 1st dose of vaccination to 30 days after the full vaccination of investigational vaccine.

16. *Participant who donated blood or lost blood ≥ 450 mL within one week before enrollment, or plans to donate blood during the period from the 1st dose of vaccination to 30 days after full vaccination of investigational vaccine;

17. Participant who cannot comply with the requirements of the study due to psychological conditions, and has a history of mental diseases or currently suffer from mental diseases;

18. Participant, who is unsuitable for participation in this study based on the investigator's judgement.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

University of Muhammadiyah Malang Hospital

UNKNOWN

Sponsor Role: collaborator

Dr. M Djamil Hospital, Padang

UNKNOWN

Sponsor Role: collaborator

Beijing Health Guard Biotechnology, Inc

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yu Hongyang

Role: STUDY_CHAIR

Beijing Health Guard Biotechnology, Inc

Locations

University of Muhammadiyah Malang Hospital

Malang, , Indonesia

Countries

Indonesia

Other Identifiers

KLWS-V502-05

Identifier Type: -

Identifier Source: org_study_id