A Study to Evaluate Different Dose Levels of GlaxoSmithKline (GSK) Biologicals' Investigational Respiratory Syncytial Virus (RSV) Vaccine (GSK3888550A), Based on the Vaccine Safety and the Antibodies (Body Defences) Produced Following Vaccine Administration, When Given to Healthy Non-pregnant Women

Healthy non-pregnant women 18-45 years of age will be randomized in a 1:1:1:1 ratio to
receive one of three dose levels (30, 60, 120 micrograms [µg]) of the investigational RSV
maternal vaccine (GSK3888550A) or placebo, administered as a single intramuscular injection
(IM).

There will be a screening visit and five study visits scheduled at Day 1 (study vaccination),
Day 8, Day 31, Day 61, and Day 91 to evaluate the primary and secondary objectives of
safety/reactogenicity and immunogenicity profiles of the 3 dose levels. Subjects will also be
contacted at Day 181. During this contact, the investigator (or delegate) will ask the
subject if she has experienced any serious adverse events (SAEs) and or any adverse events
(AEs) leading to study withdrawal since the last study visit (Day 360), as well as if she has
become pregnant during the post-vaccination period. The investigator (or delegate) will also
ask the subject about concomitant vaccinations/products/medications that she has received
since the last study visit (D91). Contact should be performed preferably via telephone. Other
means of contact (email/other) may be acceptable provided the required information can be
fully collected.

Inclusion Criteria:

- Subjects who the investigator believes will comply with the requirements of the
protocol (e.g. completion of the diary cards/questionnaires, return for follow-up
visits, have regular contact to allow evaluation during the study);

- Written informed consent obtained from the subject;

- Healthy female subjects; as established by medical history and clinical examination,
aged 18 to 45 years at the time of the vaccination;

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

- has practiced adequate contraception for 30 days prior to vaccination, and

- has a negative pregnancy test on the day of vaccination, and has agreed to
continue adequate contraception until 90 days after vaccination

Exclusion Criteria:

- Use of any investigational or non-registered product other than the study vaccine
within 30 days preceding vaccination or any planned use during the study period;

- Concurrently participating in the active phase of another clinical study, at any time
during the study period, in which the subject has been or will be exposed to an
investigational or a non-investigational vaccine/product

- Chronic administration (defined as more than 14 days in total) of immunosuppressant or
other immune-modifying drugs, as well as administration of long acting immune
modifying drugs, within 6 months prior to the vaccine dose (for corticosteroids, this
will mean prednisone higher than or equal to (≥) 5 milligrams per day (mg/day), or
equivalent). Inhaled and topical steroids are allowed;

- Administration of immunoglobulins and/or any blood products during the period starting
3 months before the study vaccination, or planned administration until 90 days
post-vaccination;

- Planned administration/administration of a vaccine not foreseen by the study protocol
within the period starting 30 days before and ending 30 days after study vaccination,
with the exception of any licensed influenza vaccine which may be administered ≥ 15
days before or after study vaccination;

- Previous experimental vaccination against RSV;

- Presence of neurological or psychiatric diagnoses which, although stable, are deemed
by the investigator to render the potential subject unable/unlikely to provide
accurate safety reports;

- Family history of congenital or hereditary immunodeficiency;

- Any confirmed or suspected immunosuppressive or immunodeficient condition, based on
medical history and physical examination;

- History of allergic disease or reactions likely to be exacerbated by any component of
the vaccine;

- Any acute or chronic, clinically significant disease, as determined by physical
examination, laboratory screening tests, subject personal report and/or health care
provider information. The following conditions will be exclusionary:

- Diabetes mellitus,

- Respiratory diseases, such as:

- Chronic Pulmonary diseases, including Chronic Obstructive Pulmonary Disease
(COPD),

- Bronchopulmonary dysplasia (note: history of past bronchopulmonary dysplasia
as a neonate/infant will not be exclusionary),

- Uncontrolled asthma or asthma necessitating treatment with chronic systemic
glucocorticoids

- Significant and/or uncontrolled psychiatric illness:

- hospitalization for psychiatric illness, history of suicide attempt(s) or
confinement for danger to self or others within 10 years

- clinically significant depression

- Major neurological disease including:

- seizure or adulthood epilepsy (note: history of febrile convulsion in
childhood is not exclusionary)

- myasthenia gravis

- history of repetitive migraine mal/status migrainosus

- Significant cardiovascular disease, including:

- Uncontrolled arterial hypertension,

- Congenital heart disease (with the exception of corrected atrial or
ventricular septal defects),

- Previous myocardial infarction,

- Valvular heart disease or history of rheumatic fever,

- Previous bacterial endocarditis,

- History of cardiac surgery (with the exception of corrected atrial or
ventricular septal defects),

- Personal or family history of cardiomyopathy or sudden adult death.

- Known or suspected Hepatitis B or Hepatitis C infection,

- Any other significant uncontrolled medical illness, defined as any illness
requiring new medical and/or surgical treatment or significant modification of
treatment dose due to uncontrolled symptoms or drug toxicity, within 3 months
prior to study vaccination.

- History of or current autoimmune disease;

- Body mass index (BMI) > 40 Kilograms (kg)/square meters(m^2);

- Pregnant or lactating female;

- Female planning to become pregnant or planning to discontinue contraceptive
precautions;

- Hypersensitivity to latex;

- Lymphoproliferative disorder or malignancy within previous 5 years;

- Acute disease and/or fever at the time of enrolment;

- Fever is defined as temperature ≥ 38°C/100.4°F

- For subjects with acute disease and/or fever at the time of enrolment, Visit 1
will be rescheduled within the allowed window for the visit.

- Subjects with fever at screening may be re-screened 1 time at a later date.

- Subjects with a minor illness (such as mild diarrhoea, mild upper respiratory
infection) without fever may be enrolled at the discretion of the investigator.

- Any clinically significant or any ≥ Grade 2* haematological (haemoglobin level, white
blood cell, lymphocyte, neutrophil, eosinophil, and platelets) and biochemical
(alanine aminotransferase [ALT] aspartate aminotransferase [AST], creatinine, blood
urea nitrogen [BUN]) laboratory abnormality detected at the last screening blood
sampling; *Grading of laboratory parameters will be based on the FDA Guidance for
Industry "Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled
in Preventive Vaccine Clinical Trials".

For Grade 1 laboratory abnormalities, the investigator should use clinical judgement to
decide which ones are clinically relevant.

Subjects with haematological/biochemical values out of normal range at screening which are
expected to be temporary, may be re-screened 1 time at a later date.

- Any other condition that the investigator judges may interfere with study procedures
or findings;

- Any medical condition that in the judgment of the investigator would make
intramuscular injection unsafe;

- Alcoholism, drug abuse and/or use disorder within the past two years (as defined in
Diagnostic and Statistical Manual of Mental Disorders [DSM-5] Diagnostic Criteria);

- Planned move to a location that will prohibit participating in the trial until study
end.