Safety and Efficacy of GSK Neisseria Gonorrhoeae GMMA (NgG) Investigational Vaccine When Administered to Healthy Adults 18 to 50 Years of Age.
Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
Details and patient eligibility
About
The aim of this first time in human proof of concept (FTiH-PoC) study is to evaluate safety and reactogenicity, to demonstrate efficacy and to explore immunogenicity of GlaxoSmithKline's (GSK) Neisseria gonorrhoeae generalized modules for membrane antigens (GMMA) (NgG) investigational vaccine compared to placebo (saline).
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Inclusion criteria for the dose-escalation safety lead-in part
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Participants, who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
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Written or witnessed/thumb printed informed consent obtained from the participant prior to performance of any study-specific procedure.
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Healthy participants as established by medical history, clinical examination, and laboratory assessment.
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A participant between and including 18 and 50 years of age at the time of informed consent.
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Female participants of non-childbearing potential may be enrolled in the study.
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Female participants of childbearing potential may be enrolled in the study if the participant:
- has practiced adequate contraception for 1 month 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 1 month after completion of the study intervention administration series.
Inclusion criteria for the efficacy PoC part
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Participants, who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
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Written or witnessed/thumb printed informed consent obtained from the participant prior to performance of any study-specific procedure.
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Healthy participants as established by:
- For the 2 intensive safety monitoring subsets (i.e., first 30 HIV negative subjects per group followed by first 8 HIV positive subjects per group): medical history, clinical examination, and laboratory assessment.
- For all the remaining participants: medical history, clinical examination.
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At risk for gonococcus infections based on sexual behavioral characteristics: this may include men having sex with men, pre-exposure prophylaxis for HIV users, individuals who engage in transactional sex participants with current or past STI diagnosis, participants at time of STI screening or seeking other STI services.
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A participant between and including 18 and 50 years of age at the time of informed consent. Transgender men and women, and other gender non-conforming people who identify themselves as neither men nor women may be enrolled into the study, based on their risk factors. For the purpose of this study, they will be followed up according to their biological sex (sex at birth), sexual orientation, and genital/sexual anatomy
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Participants of non-childbearing potential may be enrolled in the study. This includes transmen that have not undergone gender affirming surgery of their genitals.
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Participants of childbearing potential may be enrolled in the study if the participant:
- has practiced adequate contraception for 1 month 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 1 month after completion of the study intervention administration series.
Exclusion criteria
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Medical conditions Dose-escalation safety lead-in part
- Any clinically significant biochemical laboratory abnormality.
- Any other clinical condition as determined by the investigator, that may increase participant's risk due to study participation.
- History of any reaction/hypersensitivity likely to be exacerbated by any component of the study intervention.
- Confirmed or suspected immunosuppressive/immunodeficient condition, based on medical history and physical examination.
- Hypersensitivity to latex.
- Acute/chronic clinically significant pulmonary, cardiovascular, hepatic/renal functional abnormality, as determined by physical examination/laboratory tests.
- Uncontrolled neurological disorders or seizures.
- History of invasive meningococcal disease. Efficacy PoC part: HIV negative intensive safety monitoring, HIV negative full enrollment and for all remaining participants
- Persons under guardianship or trusteeship.
- Persons deprived of liberty.
- Gonococcal infection identified within 14 days prior to randomization.
- Any other clinical condition as determined by the investigator, that may increase participant's risk due to study participation.
- History of severe allergic reactions and/anaphylaxis, or any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention(s).
- Bleeding diathesis / any other condition that would contraindicate intramuscular administration.
- Confirmed or suspected immunosuppressive/immunodeficient condition, based on medical history and physical examination.
- Known seropositivity for HIV infection, regardless of viremia and CD4 cell count
- Hypersensitivity to latex.
- Acute/chronic clinically significant pulmonary, cardiovascular, hepatic/renal functional abnormality, as determined by physical examination/laboratory tests.
- Recurrent history/uncontrolled neurological disorders or seizures.
- History of invasive meningococcal disease.
The exclusion criteria depicted above, and the following exclusions criterion applies only for the HIV positive participants (intensive safety monitoring subset and full enrollment of HIV positive participants):
Seropositivity for HIV infection if:
- CD4 cell count < 350 cells/mm3 in the last 6 months
- viral load > 50cp/ml in the last 6 months
- participant is not on antiretroviral therapy (ART) for > 3 months or has switched from a different ART in the last 3 months.
For both Intensive safety monitoring subset (first 30 HIV negative subjects per group and first 8 HIV positive subjects per group) these criteria apply:
Any clinically significant hematological/biochemical laboratory abnormality.
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Prior/Concomitant therapy Applicable for both the dose-escalation safety lead-in part and the PoC part
- Use of any investigational/non-registered product other than the study intervention(s) within 30 days before the first dose/planned use during the study period.
- Previous and planned vaccination with an OMV based Neisseria meningitidis group B vaccine (e.g., Bexsero, MeNZB vaccine or MenBvac at any time prior to first dose and during the entire study period.
- Planned administration/administration of a vaccine not specified in study protocol within 15 days before the first dose and ending 15 days after the last dose of vaccine administration.
- Administration of long-acting immune-modifying drugs during the period starting 6 months prior to the first dose of study intervention/planned administration at any time during the study period.
- Administration of immunoglobulins /any blood products/plasma derivatives during the period starting 3 months before the administration of the first dose of study intervention/planned administration during the study period.
- Chronic administration (more than 14 days in total) of immunosuppressants/other immune-modifying drugs during the period starting 3 months prior to the first study intervention dose(s). For corticosteroids, this will mean prednisone equivalent ≥20 mg/day for adult participants/ ≥0.5 mg/kg/day. Inhaled and topical steroids are allowed.
The following criterion applies only for the PoC part:
•Chronic/long-term use of systemic antibiotics with an activity against Neisseria gonorrhoeae.
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Prior/Concurrent clinical study experience applicable for both dose-escalation safety lead-in part and the PoC part Concurrently participating in another clinical study, at any time during the study period, in which the participant has been/will be exposed to an investigational/a non-investigational intervention.
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Other exclusions applicable for both dose-escalation safety leading part and the PoC part
- Pregnant/lactating female.
- Female planning to become pregnant/to discontinue contraceptive precautions before 1 month after completion of the study intervention administration series.
- Any study personnel/their immediate dependents, family/household members.
- Lifestyle consideration that may interfere with the conduct of the study/pose additional risks to the rights and wellbeing of participants.
Trial design
Primary purpose
Allocation
Interventional model
Masking
1,004 participants in 9 patient groups, including a placebo group
Trial contacts and locations
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Central trial contact
US GSK Clinical Trials Call Center; EU GSK Clinical Trials Call Center
Data sourced from clinicaltrials.gov
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