- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07663032
A Study to Evaluate the Safety, Reactogenicity, and Immune Response of the GSK Vaccines Institute for Global Health (GVGH) Quadrivalent Pan-Salmonella Vaccine With and Without Alum in Healthy Young Adults
A Phase 1, Randomized, Controlled, Observer-blind Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of the GVGH Quadrivalent Pan-Salmonella Vaccine With and Without Alum in Healthy Adults 18 to 45 Years of Age in Africa
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: US GSK Clinical Trials Call Center
- Telefoonnummer: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Studie Contact Back-up
- Naam: EU GSK Clinical Trials Call Center
- Telefoonnummer: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Studie Locaties
-
-
-
Bloemfontein, Zuid-Afrika, 9301
- Werving
- GSK Investigational Site
-
Contact:
- US GSK Clinical Trials Call Center
- Telefoonnummer: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
-
Contact:
- EU GSK Clinical Trials Call Centre
- Telefoonnummer: +44 (0) 20 8990 4466
- E-mail: GSKClinicalSupportHD@gsk.com
-
Hoofdonderzoeker:
- Edrich Krantz
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Participants who, in the opinion of the Investigator, can and will comply with the requirements of the protocol (e.g., completion of the Diary cards, return for follow-up visits).
- Written informed consent obtained from the participant prior to performance of any study specific procedure.
Healthy participants as established by medical history, clinical examination, and laboratory assessment*.
*Hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibodies, and human immunodeficiency virus (HIV) antibodies will also be tested at Screening.
- A male or female between and including 18 to 45 years of age at the time of the first study intervention administration, and no older than 45 years of age at second dose administration.
- Female participants of nonchildbearing potential may be enrolled in the study. Nonchildbearing potential is defined as pre-menarche, current bilateral tubal ligation or occlusion, hysterectomy, bilateral ovariectomy, or menopause.
Participants of childbearing potential may be enrolled in the study if the participant:
- Has practiced adequate contraception (as indicated in Section 10.5) for at least 30 days prior to study intervention administration, and
- Has a negative pregnancy test within 24 hours prior to the study intervention administration, and
- Has agreed to continue adequate contraception during the entire treatment period and for 8 weeks after completion of the study intervention administration series.
- Negative HLA-B27 testing.
- Body mass index of 18>= to <=30 kg/m2 at Screening.
- Living in the study area and plan to remain in the study area for the study duration.
Exclusion Criteria:
Medical Conditions:
- Known exposure to S. Typhi, S. Paratyphi A, and non-typhoidal Salmonella confirmed by blood culture during the period starting 3 years prior to first study intervention administration as confirmed using medical history.
- History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention.
- Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination (no laboratory testing required).
- Acute or chronic clinically significant pulmonary, cardiovascular, hepatic, or renal functional abnormality, as determined by physical examination or laboratory screening tests.
- Recurrent history or uncontrolled neurological disorders or seizures.
- Any clinically significant hematological and/or biochemical laboratory abnormality.
- Clinical conditions representing a contraindication to intramuscular (IM) injections and/or blood draws.
- Any behavioral or cognitive impairment or psychiatric disease that in the opinion of the Investigator, may interfere with the participant's ability to participate in the study.
- Acute or chronic illness which may be severe enough to preclude participation.
Any other clinical condition that, in the opinion of the Investigator, might pose additional risk to the participant due to participation in the study.
Prior/Concomitant Therapy:
- History of receiving any typhoid vaccine (Ty21a, Vi capsular polysaccharide, or TCV) in the participant's life.
- History of receiving any investigational iNTS, S. Paratyphi A, or GMMA vaccines in the participant's life.
Use of any investigational or non-registered product (drug, vaccine, or medical device) other than the study interventions during the period beginning 30 days (Days -30 to 1) before the first dose of study interventions, or their planned use during the study period.
Use of herbs and traditional treatments is not considered an exclusion criterion.
- A vaccine not foreseen by the study protocol administered during the period starting at 14 days before the first dose and ending 30 days after the last dose of study interventions administration, with the exception of flu vaccines or Coronavirus disease 2019 vaccine.
- Administration of long-acting immune-modifying drugs (e.g., infliximab) at any time during the study period.
- Administration of immunoglobulins and/or any blood products or plasma derivatives during the period starting 3 months before the administration of the first dose of study interventions or planned administration during the study period.
Chronic administration (defined as more than 14 days in total) of immunosuppressants or other immune-modifying drugs during the period starting 3 months prior to the first study intervention dose(s). For corticosteroids, this will be prednisone equivalent >=20 mg/day for adult participants. Inhaled and topical steroids are allowed.
Prior/Concurrent Clinical Study Experience:
Concurrently participating in another clinical study, at any time during the study period, in which the participant has been or will be exposed to an investigational or a non-investigational intervention (vaccine and drug).
Other Exclusions:
- Pregnant or lactating female.
- Female planning to become pregnant or planning to discontinue contraceptive precautions.
- History of/current chronic alcohol consumption and/or drug abuse. This will be decided at the discretion of the Investigator.
- Any study personnel or their immediate dependents, family, or household members.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Sequentiële toewijzing
- Masker: Verdrievoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Pan-Salmonella with Alum (Low dose) Group
Participants will receive the low dose level of the candidate Pan-Salmonella-with-aluminium-hydroxide (Alum) vaccine at Days 1, 61 and 181.
|
Participants receive low dose of the Pan-Salmonella-with-Alum.
|
|
Experimenteel: Pan-Salmonella with Alum (Full dose) Group
Participants will receive the full dose level of the candidate Pan-Salmonella-with-Alum vaccine at Days 1, 61 and 181.
|
Participants receive full dose of the Pan-Salmonella-with-Alum.
|
|
Experimenteel: Pan-Salmonella without Alum (Low dose) Group
Participants will receive the low dose level of the candidate Pan-Salmonella-without-Alum vaccine at Days 1, 61 and 181.
|
Participants receive low dose of the Pan-Salmonella-without-Alum.
|
|
Experimenteel: Pan-Salmonella without Alum (Full dose) Group
Participants will receive the full dose level of the candidate Pan-Salmonella-without-Alum vaccine at Days 1, 61 and 181.
|
Participants receive full dose of the Pan-Salmonella-without-Alum.
|
|
Placebo-vergelijker: Control Group
Participants will receive placebo at Days 1 and 181, and Typhoid Vi conjugate vaccine at Day 61.
|
Participants receive Typhoid Vi conjugate vaccine as control
Andere namen:
Participants receive Placebo (saline solution) as control.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of participants with solicited administration site events
Tijdsspanne: From Day 1 to Day 7
|
Assessed solicited administration site events will be pain, redness and swelling.
|
From Day 1 to Day 7
|
|
Number of participants with solicited administration site events
Tijdsspanne: From Day 61 to Day 67
|
From Day 61 to Day 67
|
|
|
Number of participants with solicited administration site events
Tijdsspanne: From Day 181 to Day 187
|
From Day 181 to Day 187
|
|
|
Number of participants with solicited systemic events
Tijdsspanne: From Day 1 to Day 7
|
Assessed solicited systemic events will be fever, headache, myalgia, arthralgia and fatigue.
|
From Day 1 to Day 7
|
|
Number of participants with solicited systemic events
Tijdsspanne: From Day 61 to Day 67
|
From Day 61 to Day 67
|
|
|
Number of participants with solicited systemic events
Tijdsspanne: From Day 181 to Day 187
|
From Day 181 to Day 187
|
|
|
Number of participants with unsolicited events
Tijdsspanne: From Day 1 to Day 30
|
An unsolicited adverse event (AE) is an AE that was either not included in the list of solicited AEs, or could.
be included in the list of solicited AEs but with an onset outside the specified period of.
follow-up for solicited AEs.
Unsolicited AEs must have been communicated by participants who have signed informed consent.
Unsolicited AEs include serious and non-serious AEs.
|
From Day 1 to Day 30
|
|
Number of participants with unsolicited events
Tijdsspanne: From Day 61 to Day 91
|
From Day 61 to Day 91
|
|
|
Number of participants with unsolicited events
Tijdsspanne: From Day 181 to Day 211
|
From Day 181 to Day 211
|
|
|
Number of participants with serious adverse events (SAEs)
Tijdsspanne: From Day 1 to Day 211
|
An SAE is defined as any untoward medical occurrence that, at any dose, results in persistent or significant disability/incapacity, requires inpatient hospitalization or prolongation of existing hospitalization, is life-threatening, or results in death.
|
From Day 1 to Day 211
|
|
Number of participants with adverse events (AEs) or SAEs leading to withdrawal from the study or discontinuation of study intervention
Tijdsspanne: From Day 1 to Day 211
|
From Day 1 to Day 211
|
|
|
Number of participants with changes from baseline or changes from normal values for hematological, renal, and hepatic panels test results
Tijdsspanne: At Day 8
|
At Day 8
|
|
|
Number of participants with changes from baseline or changes from normal values for hematological, renal, and hepatic panels test results
Tijdsspanne: At Day 68
|
At Day 68
|
|
|
Number of participants with changes from baseline or changes from normal values for hematological, renal, and hepatic panels test results
Tijdsspanne: At Day 188
|
At Day 188
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of participants with serious adverse events (SAEs)
Tijdsspanne: From Day 211 to Day 361
|
From Day 211 to Day 361
|
|
|
Number of participants with AEs/SAEs leading to withdrawal from the study or discontinuation of study intervention
Tijdsspanne: From Day 211 to Day 361
|
From Day 211 to Day 361
|
|
|
Geometric mean concentration (GMC) of anti-serotype specific immunoglobulin G (IgG) antibody
Tijdsspanne: Pre-intervention at Day 1, Day 61 and Day 181
|
The GMC will be determined using Enzyme-linked immunosorbent assay (ELISA).
|
Pre-intervention at Day 1, Day 61 and Day 181
|
|
Adjusted GMC of anti-serotype specific IgG antibody
Tijdsspanne: Pre-intervention at Day 1, Day 61 and Day 181
|
Pre-intervention at Day 1, Day 61 and Day 181
|
|
|
GMC of anti-serotype specific IgG antibody
Tijdsspanne: At Day 31, Day 91 and Day 211
|
At Day 31, Day 91 and Day 211
|
|
|
Adjusted GMC of anti-serotype specific IgG
Tijdsspanne: At Day 31, Day 91 and Day 211
|
At Day 31, Day 91 and Day 211
|
|
|
Number of participants with anti-serotype specific IgG antibody concentration fold increase
Tijdsspanne: At Day 31, Day 91 and Day 211 compared with baseline (Day 1)
|
At least a 4-fold rise will be evaluated.
|
At Day 31, Day 91 and Day 211 compared with baseline (Day 1)
|
|
Number of participants with Anti-Vi Ag IgG antibody concentrations
Tijdsspanne: Pre-dose at Day 1, Day 61 and Day 181
|
The concentration considered will be equivalent to ≥4.3 microgram per milliliter (μg/mL).
|
Pre-dose at Day 1, Day 61 and Day 181
|
|
Number of participants with Anti-Vi Ag IgG antibody concentrations
Tijdsspanne: At Day 31, Day 91 and Day 211
|
The concentration considered will be equivalent to ≥4.3 μg/mL
|
At Day 31, Day 91 and Day 211
|
|
Number of participants with Anti-Vi Ag IgG antibody concentrations
Tijdsspanne: Pre-dose at Day 1, Day 61 and Day 181
|
The concentration considered will be ≥2.0 μg/mL
|
Pre-dose at Day 1, Day 61 and Day 181
|
|
Number of participants with Anti-Vi Ag IgG antibody concentrations
Tijdsspanne: At Day 31, Day 91 and Day 211
|
The concentration considered will be ≥2.0 μg/mL.
|
At Day 31, Day 91 and Day 211
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 300281
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
IPD-tijdsbestek voor delen
IPD-toegangscriteria voor delen
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
- ICF
- MVO
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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 .