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- Klinische proef NCT07616934
A Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-A1 in Healthy Young Adults
15 juni 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Werving
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
80
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Clinical Development
- Telefoonnummer: 650-837-0111
- E-mail: Clinicaltrialsgov@vaxcyte.com
Studie Locaties
-
-
South Australia
-
Adelaide, South Australia, Australië, 5067
- Werving
- Fusion Clinical Research
-
Contact:
- Christopher D Rook, MD
- Telefoonnummer: +61 8 7088 7900
- E-mail: christopher.rook@cmax.com.au
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Hoofdonderzoeker:
- Christopher Rook, MD
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Ja
Beschrijving
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
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 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
|
|
Experimenteel: 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
|
|
Experimenteel: 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
|
|
Placebo-vergelijker: 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
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Frequency of solicited local reactions (redness, swelling, and pain at injection site)
Tijdsspanne: up to 7 days after each vaccination
|
up to 7 days after each vaccination
|
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Frequency of solicited systemic adverse events (AE) (fever, headache, fatigue, muscle pain, rash, joint pain, nausea/vomiting, diarrhea)
Tijdsspanne: 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
Tijdsspanne: 7 days after each vaccination
|
7 days after each vaccination
|
|
Frequency of unsolicited AE
Tijdsspanne: up to 30 days after each vaccination
|
up to 30 days after each vaccination
|
|
Frequency of medically attended AE (MAAE)
Tijdsspanne: Up to 8 months after first vaccination
|
Up to 8 months after first vaccination
|
|
Frequency of new onset chronic illness (NOCI)
Tijdsspanne: up to 8 months after the first vaccination
|
up to 8 months after the first vaccination
|
|
Frequency of serious adverse events (SAE)
Tijdsspanne: 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])
Tijdsspanne: up to 8 months after the first vaccination
|
up to 8 months after the first vaccination
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Median value of each safety laboratory parameter assessed 7 days after each vaccination
Tijdsspanne: 7 days after each vaccination
|
7 days after each vaccination
|
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Median change from baseline to 7 days after each vaccination for each safety laboratory parameter
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: Prior to each vaccination, 1 month after each vaccination and Month 8
|
Prior to each vaccination, 1 month after each vaccination and Month 8
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 juni 2026
Primaire voltooiing (Geschat)
1 december 2027
Studie voltooiing (Geschat)
1 december 2027
Studieregistratiedata
Eerst ingediend
18 mei 2026
Eerst ingediend dat voldeed aan de QC-criteria
26 mei 2026
Eerst geplaatst (Werkelijk)
1 juni 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
16 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
15 juni 2026
Laatst geverifieerd
1 juni 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- VAXA1-101
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
JA
Beschrijving IPD-plan
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.
IPD-toegangscriteria voor delen
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.
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .