- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07616934
A Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-A1 in Healthy Young Adults
15 czerwca 2026 zaktualizowane przez: 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.
Przegląd badań
Status
Rekrutacyjny
Warunki
Interwencja / Leczenie
Typ studiów
Interwencyjne
Zapisy (Szacowany)
80
Faza
- Faza 1
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
- Nazwa: Clinical Development
- Numer telefonu: 650-837-0111
- E-mail: Clinicaltrialsgov@vaxcyte.com
Lokalizacje studiów
-
-
South Australia
-
Adelaide, South Australia, Australia, 5067
- Rekrutacyjny
- Fusion Clinical Research
-
Kontakt:
- Christopher D Rook, MD
- Numer telefonu: +61 8 7088 7900
- E-mail: christopher.rook@cmax.com.au
-
Główny śledczy:
- Christopher Rook, MD
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
Akceptuje zdrowych ochotników
Tak
Opis
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 studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Zapobieganie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: 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
|
|
Eksperymentalny: 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
|
|
Eksperymentalny: 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
|
|
Komparator placebo: 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
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Ramy czasowe |
|---|---|
|
Frequency of solicited local reactions (redness, swelling, and pain at injection site)
Ramy czasowe: up to 7 days after each vaccination
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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)
Ramy czasowe: up to 7 days after each vaccination
|
up to 7 days after each vaccination
|
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Frequency of laboratory abnormalities identified from protocol-scheduled safety laboratory assessments at 7 days after each vaccination and reported as AE
Ramy czasowe: 7 days after each vaccination
|
7 days after each vaccination
|
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Frequency of unsolicited AE
Ramy czasowe: up to 30 days after each vaccination
|
up to 30 days after each vaccination
|
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Frequency of medically attended AE (MAAE)
Ramy czasowe: Up to 8 months after first vaccination
|
Up to 8 months after first vaccination
|
|
Frequency of new onset chronic illness (NOCI)
Ramy czasowe: up to 8 months after the first vaccination
|
up to 8 months after the first vaccination
|
|
Frequency of serious adverse events (SAE)
Ramy czasowe: 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])
Ramy czasowe: up to 8 months after the first vaccination
|
up to 8 months after the first vaccination
|
Miary wyników drugorzędnych
Miara wyniku |
Ramy czasowe |
|---|---|
|
Median value of each safety laboratory parameter assessed 7 days after each vaccination
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: Prior to each vaccination, 1 month after each vaccination and Month 8
|
Prior to each vaccination, 1 month after each vaccination and Month 8
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
1 czerwca 2026
Zakończenie podstawowe (Szacowany)
1 grudnia 2027
Ukończenie studiów (Szacowany)
1 grudnia 2027
Daty rejestracji na studia
Pierwszy przesłany
18 maja 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
26 maja 2026
Pierwszy wysłany (Rzeczywisty)
1 czerwca 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
16 czerwca 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
15 czerwca 2026
Ostatnia weryfikacja
1 czerwca 2026
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- VAXA1-101
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
TAK
Opis planu 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.
Kryteria dostępu do udostępniania 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.
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
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