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A Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-A1 in Healthy Young Adults

15 de junio de 2026 actualizado por: Vaxcyte, Inc.

A Phase 1, First-in-Human, Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-A1 in Healthy Young Adults

This is a phase 1, first-in-human, randomized, double-blind, placebo-controlled, dose-escalation study to evaluate the safety, tolerability, and immunogenicity of VAX-A1 in healthy adults 18-40 years of age.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

80

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • South Australia
      • Adelaide, South Australia, Australia, 5067
        • Reclutamiento
        • Fusion Clinical Research
        • Contacto:
        • Investigador principal:
          • Christopher Rook, MD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Individuals 18-40 years of age (inclusive) at the time of randomization into the study
  • Able and willing to complete the informed consent process
  • Available for clinical follow-up through the last study visit at 6 months post-Dose 2
  • Willing to have blood samples collected, stored indefinitely, and be used for research purposes
  • Able to provide proof of identity to the satisfaction of the study staff completing the enrollment process
  • Healthy, as defined by absence of clinically significant medical condition, either acute or chronic, as determined by medical history, vital signs, physical examination, screening laboratory test results, TTE and ECG results, and clinical assessment by the Investigator
  • For applicable individuals, postmenopausal (as confirmed by follicle-stimulating hormone [FSH] level at Screening) for at least 1 year, or surgically sterile for at least 6 months prior to dosing
  • Individuals of childbearing potential must be not pregnant and not lactating, must have negative urine and serum pregnancy tests at Screening and a negative urine pregnancy test immediately prior to randomization, and agree to use acceptable contraception if heterosexually active. Participants must agree to consistently practice contraception if sexually active at least 7 days prior to enrollment and throughout the duration of the study
  • Able to access and use a smartphone, tablet, computer, or other device connected to Wi-Fi or cellular network for completion of an eDiary

Exclusion Criteria:

  • History of any clinically important cardiac, rheumatologic, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal, or other disease as determined by the Investigator. This includes a history of polyarthritis, nephropathy, pericarditis, myocarditis, or hypertension requiring current pharmacologic treatment.
  • History of invasive GAS infection (such as toxic shock syndrome, necrotizing fasciitis, bloodstream infection, pleural empyema, meningitis) or poststreptococcal immune mediated disease (such as RHD, ARF, or APSGN)
  • Known or suspected autoimmune disease, collagen vascular disease, or impairment/alteration of immune function (e.g., congenital or acquired immunodeficiency)
  • Previous or existing diagnosis of human immunodeficiency virus, Hepatitis B virus, or Hepatitis C virus, or a positive serologic test at Screening
  • History of malignancy or neoplasm, except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer
  • Bleeding disorder diagnosed by a physician (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions) resulting in clinically significant bruising or bleeding difficulties with IM injections or blood draws
  • History of severe allergic reaction with generalized urticaria, angioedema, or anaphylaxis to any previous vaccination
  • Oral temperature >38.0°C (>100.4°F) or acute illness within 3 days prior to study vaccination (subject may be rescreened)
  • Confirmed elevated BP at Screening, defined as systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg measured seated after ≥5 minutes rest and confirmed by repeat measurement
  • Physical examination indicating any clinically significant medical condition or inadequate venous access
  • Any Grade ≥2 abnormal safety laboratory test at Screening
  • Abnormal ESR, or CRP or C3 levels at Screening
  • Confirmed microscopic hematuria (>10 RBC/mm³) on UA at Screening. If a potential confounder is present, a repeat UA may be performed during the Screening window; exclusion applies to confirmed microscopic hematuria on an evaluable specimen.
  • Evidence of antecedent/recent GAS infection based on anti-DNase B titer ≥ the laboratory reported upper limit of normal (ULN) for the assay used at Screening. Participants with anti-DNase B titer ≥0.8×ULN and <ULN at the initial Screening visit are temporarily ineligible and may be re-screened with repeat anti-DNase B testing 7-21 days after the initial sample; participants will be excluded if the repeat anti-DNase B titer is ≥ULN or demonstrates a clinically meaningful increase of ≥20% relative to the initial screening value, in the absence of an alternative explanation.
  • Positive GAS rapid NAAT at Screening or Day 1
  • Any finding based on comprehensive TTE at Screening indicative of possible cardiac pathology, including valvular abnormalities defined as mild stenosis or regurgitation.
  • Any finding on ECG that is indicative of possible cardiac pathology, including a prolonged PR interval or conduction abnormality
  • Receipt of any investigational product within 30 days prior to enrollment into the study, currently participating in another study that includes receipt of an investigational product or procedure, or having plans to receive another investigational product(s) while on study
  • Planned or actual administration of any licensed vaccine within 30 days before or after receipt of study vaccine, or within 14 days before or after receipt of study vaccine in the case of influenza and COVID-19 vaccines. Vaccines that are required emergently (e.g., tetanus vaccination in a participant with a contaminated wound) may be given at any time during the study.
  • Received blood or blood product (including intravenous immunoglobulin) within 6 months of enrollment into the study
  • Receipt of any immunosuppressive therapy, including systemic steroids at a dosage equivalent to ≥0.5 mg/kg/day of prednisone, chronic use of inhaled or nebulized high potency corticosteroids, or use of intra-articular or intrabursal corticosteroids within 1 year of the first study vaccination
  • Body mass index (BMI) ≥32 kg/m2 or ≤18 kg/m2
  • History of alcohol or drug abuse in the 5 years prior to enrollment, or any history of intravenous drug abuse
  • Any medical, psychiatric, or social condition that in the judgment of the Investigator may interfere with the study objectives, impair a participant's ability to give informed consent, pose a risk to the participant, or prevent the participant from completing the study
  • Employee of, or first degree relative of any person employed by the Sponsor, the contract research organization (CRO), the Investigator, study site personnel, or site

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: VAX-A1 Low
Participants will receive 2 doses of VAX-A1 administered via intramuscular injection at Day 1 and Month 2
0.5mL of the low dose VAX-A1 will be administered into the deltoid muscle
Experimental: VAX-A1 Mid
Participants will receive 2 doses of VAX-A1 administered via intramuscular injection at Day 1 and Month 2
0.5mL of the mid dose VAX-A1 will be administered into the deltoid muscle
Experimental: VAX-A1 High
Participants will receive 2 doses of VAX-A1 administered via intramuscular injection at Day 1 and Month 2
0.5mL of the high dose VAX-A1 will be administered into the deltoid muscle
Comparador de placebos: Placebo
Participants will receive 2 doses of placebo administered via intramuscular injection at Day 1 and Month 2
0.5mL of placebo (normal saline) will be administered into the deltoid muscle

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Frequency of solicited local reactions (redness, swelling, and pain at injection site)
Periodo de tiempo: up to 7 days after each vaccination
up to 7 days after each vaccination
Frequency of solicited systemic adverse events (AE) (fever, headache, fatigue, muscle pain, rash, joint pain, nausea/vomiting, diarrhea)
Periodo de tiempo: up to 7 days after each vaccination
up to 7 days after each vaccination
Frequency of laboratory abnormalities identified from protocol-scheduled safety laboratory assessments at 7 days after each vaccination and reported as AE
Periodo de tiempo: 7 days after each vaccination
7 days after each vaccination
Frequency of unsolicited AE
Periodo de tiempo: up to 30 days after each vaccination
up to 30 days after each vaccination
Frequency of medically attended AE (MAAE)
Periodo de tiempo: Up to 8 months after first vaccination
Up to 8 months after first vaccination
Frequency of new onset chronic illness (NOCI)
Periodo de tiempo: up to 8 months after the first vaccination
up to 8 months after the first vaccination
Frequency of serious adverse events (SAE)
Periodo de tiempo: from screening through up to 8 months after first vaccination
from screening through up to 8 months after first vaccination
Occurrence of AE of special interest (AESI) (acute rheumatic fever [ARF], acute carditis [AC], and acute glomerulonephritis [AGN])
Periodo de tiempo: up to 8 months after the first vaccination
up to 8 months after the first vaccination

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Median value of each safety laboratory parameter assessed 7 days after each vaccination
Periodo de tiempo: 7 days after each vaccination
7 days after each vaccination
Median change from baseline to 7 days after each vaccination for each safety laboratory parameter
Periodo de tiempo: 7 days after each vaccination
7 days after each vaccination
Serum IgG geometric mean titer (GMT) at each scheduled immunogenicity sample collection visit for each vaccine antigen (SLO, C5a pep, SpyAD, GAC)
Periodo de tiempo: Prior to each vaccination, 1 month after each vaccination and Month 8
Prior to each vaccination, 1 month after each vaccination and Month 8
Serum IgG geometric mean fold rise (GMFR) from baseline to each scheduled post-vaccination immunogenicity sample collection visit for each vaccine antigen (SLO, C5a pep, SpyAD, GAC)
Periodo de tiempo: Prior to each vaccination, 1 month after each vaccination and Month 8
Prior to each vaccination, 1 month after each vaccination and Month 8
Percentage of participants achieving serum IgG ≥2-fold increase from baseline at each scheduled post-vaccination immunogenicity sample collection visit for each vaccine antigen (SLO, C5a pep, SpyAD, GAC)
Periodo de tiempo: 1 month after each vaccination and Month 8
1 month after each vaccination and Month 8
Percentage of participants with serum IgG ≥ LLOQ of the assay at each scheduled immunogenicity sample collection visit for each vaccine antigen (SLO, C5a pep, SpyAD, GAC)
Periodo de tiempo: Prior to each vaccination, 1 month after each vaccination and Month 8
Prior to each vaccination, 1 month after each vaccination and Month 8

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de junio de 2026

Finalización primaria (Estimado)

1 de diciembre de 2027

Finalización del estudio (Estimado)

1 de diciembre de 2027

Fechas de registro del estudio

Enviado por primera vez

18 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

26 de mayo de 2026

Publicado por primera vez (Actual)

1 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

15 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

Vaxcyte is committed to providing access to anonymized data from the company's clinical trials for the purpose of legitimate scientific research. Requests for data may be addressed to datasharing@vaxcyte.com. Requests must be accompanied by a detailed analysis plan and will be reviewed for scientific validity. Sharing of data will require execution of a data-sharing agreement.

Criterios de acceso compartido de IPD

Criteria will depend on the specific proposal received and may include qualification of the scientific researchers, potential contribution to the research field, scientific rigor of statistical and analytical methods, and other criteria appropriate for the proposal.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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