A Phase I/II, Observer-blind, Randomised, Placebo-controlled Study to Assess Safety, Immunogenicity and Efficacy of GSK S. Aureus Candidate Vaccine When Administered to Healthy Adults (Dose-escalation) and to Adults 18 to 64 Years of Age With a Recent S. Aureus Skin and Soft Tissue Infection (SSTI)

Status: Completed
Location: See all (47) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Safety, immunogenicity and efficacy of GSK S. aureus candidate vaccine (GSK3878858A) when administered to healthy adults (dose-escalation) and to adults 18 to 64 years of age with a recent S. aureus skin and soft tissue infection (SSTI). In the dose-escalation safety lead-in phase in healthy adults safety and immunogenicity of 4 different compositions is assessed. After safety has been shown in this phase, in the second phase, proof of principle (PoP) phase of the study in adults with a recent SSTI safety, immunogenicity and efficacy of the final composition of the vaccine is assessed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 64
Healthy Volunteers: t
View:

⁃ All subjects must satisfy all the following criteria at study entry:

• Subjects 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 or witnessed informed consent obtained from the subject prior to performance of any study specific procedure.

• Subject satisfying screening requirements.

• Subjects who, after the nature of the study has been explained to them, have shown adequate comprehension of the study procedures and knowledge of study.

• A male or female

• Dose escalation and safety lead-in phase: Aged between 18 and 50 years of age, inclusive, at the time of first vaccination.

• PoP phase: Aged between 18 and 64 years of age, inclusive, at the time of first vaccination.

• Female subjects of non-childbearing potential may be enrolled in the study. Non-childbearing potential is defined as pre-menarche, current bilateral tubal ligation or occlusion, hysterectomy, bilateral ovariectomy or post-menopause.

• Female subjects of childbearing potential may be enrolled in the study, if the subject:

• has practiced adequate contraception for 30 days prior to vaccination,

• has a negative pregnancy test on the day of enrolment, and

• has agreed to continue adequate contraception during the entire treatment period and for 2 months after completion of the vaccination series.

⁃ Additional inclusion criteria only for subjects to be enrolled in the dose-escalation safety lead-in screening epoch:

• Healthy subjects as established by medical history, clinical examination and laboratory assessment.

⁃ Additional inclusion criteria only for subjects to be enrolled in the PoP screening epoch:

• Healthy subjects as established by medical history and clinical examination before entering into the study with an ongoing SSTI suspected to be caused by S. aureus, as diagnosed by investigator (before randomization subjects have to be treated until clinical resolution of culture confirmed SSTI caused by S. aureus). SSTI must be amenable to microbiological culturing per standard clinical practice (i.e. recovery of drainage sample from abscess or suppurative cellulitis).

⁃ OR

• Healthy subjects as established by medical history and clinical examination before entering into the study with an ongoing S. aureus SSTI (i.e. S. aureus is the most likely cause), as confirmed by a S. aureus positive culture performed outside the study procedures and not earlier than 30 days prior to Informed Consent Form signature. Before randomisation subjects have to be treated until clinical resolution of the culture confirmed SSTI caused by S. aureus. These subjects will be enrolled whether they have or have not already started specific treatment of the infection. In case they have not started the treatment, this will be then given in compliance with the standard medical practice for the management of S. aureus SSTIs and the choice and judgment of the most appropriate treatment will be applied by the investigator, outside the study procedures.

Locations
United States
California
GSK Investigational Site
La Mesa
GSK Investigational Site
Torrance
Illinois
GSK Investigational Site
Evanston
Kentucky
GSK Investigational Site
Lexington
GSK Investigational Site
Lexington
Louisiana
GSK Investigational Site
New Orleans
GSK Investigational Site
Slidell
North Carolina
GSK Investigational Site
Winston-salem
Nebraska
GSK Investigational Site
Omaha
Pennsylvania
GSK Investigational Site
Philadelphia
Other Locations
Australia
GSK Investigational Site
Coffs Harbour
GSK Investigational Site
Darlinghurst
GSK Investigational Site
Fortitude Valley
GSK Investigational Site
Geelong
GSK Investigational Site
Southport
GSK Investigational Site
Sydney
India
GSK Investigational Site
Ahmedabad
GSK Investigational Site
Ahmedabad
GSK Investigational Site
Ahmedabad
GSK Investigational Site
Ahmedabad
GSK Investigational Site
Kanpur
GSK Investigational Site
Kolkata
GSK Investigational Site
Lucknow
GSK Investigational Site
Nagpur
GSK Investigational Site
Nagpur
GSK Investigational Site
Pune
GSK Investigational Site
Pune
GSK Investigational Site
Thane
GSK Investigational Site
Varanasi
New Zealand
GSK Investigational Site
Christchurch
GSK Investigational Site
Grafton Auckland
GSK Investigational Site
Nawton
GSK Investigational Site
Nelson
GSK Investigational Site
New Lynn
GSK Investigational Site
Papatoetoe Auckland
Poland
GSK Investigational Site
Bialystok
GSK Investigational Site
Katowice
GSK Investigational Site
Lodz
GSK Investigational Site
Lublin
GSK Investigational Site
Szczecin
GSK Investigational Site
Warszawa
GSK Investigational Site
Warszawa
South Africa
GSK Investigational Site
Cape Town
GSK Investigational Site
Durban
GSK Investigational Site
Soweto Johannesburg
United Kingdom
GSK Investigational Site
Birmingham
GSK Investigational Site
Nottingham
Time Frame
Start Date: 2020-06-29
Completion Date: 2024-03-12
Participants
Target number of participants: 227
Treatments
Experimental: Half dose non-adj Group 1a
Subjects aged 18 to 50 at the time of first vaccination who receive 1 dose of Sa-5Ag (5 antigens of S. aureus) half dose, non-adjuvanted at Day 1.
Placebo_comparator: Placebo Group 1b
Subjects aged 18 to 50 at the time of first vaccination who receive 1 dose of placebo (saline) at Day 1.
Experimental: Full dose non-adj Group 2a
Subjects aged 18 to 50 at the time of first vaccination who receive 1 dose of Sa-5Ag (5 antigens of S. aureus) full dose, non-adjuvanted at Day 1
Placebo_comparator: Placebo Group 2b
Subjects aged 18 to 50 at the time of first vaccination who receive 1 dose of placebo (saline) at Day 1.
Experimental: Half dose adj Group 3a
Subjects aged 18 to 50 at the time of first vaccination who receive 1 dose of Sa-5Ag (5 antigens of S. aureus) half dose, adjuvanted at Day 1.
Placebo_comparator: Placebo Group 3b
Subjects aged 18 to 50 at the time of first vaccination who receive 1 dose of placebo (saline) at Day 1.
Experimental: Full dose adj Group 4a
Subjects aged 18 to 50 at the time of first vaccination who receive a series of 2 doses of S. aureus candidate vaccine (Sa-5Ag full dose adjuvanted) given approximately 2 months apart (Days 1 and 61)
Placebo_comparator: Placebo Group 4b
Subjects aged 18 to 50 at the time of first vaccination who receive a series of 2 doses of placebo (saline) given approximately 2 months apart (Days 1 and 61).
Experimental: Vaccine Group 5a
Subjects aged 18 to 64 at the time of first vaccination who receive a series of 2 doses of S. aureus candidate vaccine (Sa-5Ag full dose adjuvanted) given approximately 2 months apart (Days 1 and 61).
Placebo_comparator: Placebo Group 5b
Subjects aged 18 to 64 at the time of first vaccination who receive a series of 2 doses of placebo (saline) given approximately 2 months apart (Days 1 and 61).
Sponsors
Leads: GlaxoSmithKline

This content was sourced from clinicaltrials.gov

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