Last updated: 04/27/2021 08:00:05

GSK1325756 Relative Bioavailability Study in Healthy Elderly subjects

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GSK study ID
207573
See study documents
Clinicaltrials.gov ID
NCT03457727
See results summary
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: A Two Part, Randomized, Open-label, Cross over Study in Healthy Elderly Participants to Evaluate the Relative Bioavailability of Hydrobromide Salt Tablet Formulations of Danirixin in the Fed and Fasted States, and to Evaluate the Effect of Food and Gastric Acid Secretion Suppression on Danirixin Pharmacokinetics Following Administration of Hydrobromide Salt Tablets
Trial description: This 2-part study will be carried out on healthy elderly subjects to evaluate relative bioavailability of danirixin formulations. Part A will support the selection of the formulation and Part B will assess food effect, bioavailability and pharmacokinetic (PK) profile of selected formulation from Part A. Danirixin is currently administered with food, therefore the investigation of food effect for the selected formulation could potentially enable dosing without food. Approximately 16 subjects will be included in Part A and approximately 24 subjects will be included in Part B. Both parts will include a screening phase, treatment phase with in-between washout period and a follow-up phase.
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:

Area under the concentration-time curve (AUC) from time zero (pre-dose) extrapolated to infinite time (AUC[0-inf]) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin 475 milligrams (mg) direct comparison (DC) formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin 600 mg Hydroxypropyl Methylcellulose (HPMC) formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Maximum Observed Concentration (Cmax) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Cmax of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Cmax of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Cmax of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Number of subjects with adverse events (AEs) and serious AEs (SAEs)

Timeframe: Up to 58 days

Number of subjects with abnormal systolic blood pressure (SBP) and diastolic blood pressure (DBP) findings

Timeframe: Up to 58 days

Number of subjects with abnormal pulse rate findings

Timeframe: Up to 58 days

Number of subjects with abnormal respiratory rate findings

Timeframe: Up to 58 days

Number of subjects with abnormal body temperature findings

Timeframe: Up to 58 days

Number of subjects with abnormal electrocardiogram (ECG) findings

Timeframe: Up to 58 days

Number of subjects with abnormal clinical chemistry parameters

Timeframe: Up to 58 days

Number of subjects with abnormal clinical hematology parameters

Timeframe: Up to 58 days

Number of subjects with abnormal urinalysis parameters

Timeframe: Up to 58 days

AUC from time zero (pre-dose) to last time of quantifiable concentration (AUC[0-t]) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC from time zero (pre-dose) to 24 hours post dose (AUC[0-24]) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

AUC (0-24) of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

AUC (0-24) of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

AUC (0-24) of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

Time of occurrence of Cmax (Tmax) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Terminal phase half-life (T1/2) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Time of last quantifiable concentration (Tlast) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Lag time before observation of drug concentrations in sampled matrix (Tlag) of danirixin reference formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin 475 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin 600 mg DC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin 600 mg HPMC formulation: Part A

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-24) of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

Cmax of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin formulation administered with omeprazole (OMP): Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-24) of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

Cmax of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin formulation administered with OMP: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-inf) of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-t) of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

AUC (0-24) of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

AUC (0-24) of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24 hours post-dose on Day 1

Cmax of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Cmax of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tmax of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

T1/2 of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlast of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin reference formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Tlag of danirixin mono formulation: Part B

Timeframe: Pre-dose, 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 24, 48 hours post-dose on Day 1

Secondary outcomes:
Not applicable
Interventions:
  • Drug: Danirixin
  • Drug: Omeprazole
    • Enrollment:
    40
    Primary completion date:
    2018-25-07
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    Not applicable
    Medical condition
    Pulmonary Disease, Chronic Obstructive
    Product
    danirixin, omeprazole
    Collaborators
    Not applicable
    Study date(s)
    March 2018 to July 2018
    Type
    Interventional
    Phase
    1

    Participation criteria

    Sex
    Female & Male
    Age
    65 - 80 years
    Accepts healthy volunteers
    Yes
    • Subjects must be 65 to 80 years of age inclusive, at the Screening Visit.
    • Subjects who are healthy, as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring or a subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included if the investigator and the GlaxoSmithKline (GSK) Medical Monitor agree that the finding is unlikely to introduce risk factors and will not interfere with the study procedures and objectives. Additionally, laboratory assessments that are specifically listed in the inclusion or exclusion criteria and are outside of the reference range can be repeated once during the screening period.
    • Significant history of or current cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study treatment; or interfering with the interpretation of data.
    • Evidence of active or latent tuberculosis (TB) as documented by medical history and examination, chest x-rays (posterior anterior and lateral), and TB testing: either a positive tuberculin skin test [TST; defined as a skin induration <5 millimeter (mm) at 48 to 72 hours, regardless of Bacillus Calmette-Guerin (BCG) or other vaccination history] or a positive (not indeterminate) QuantiFERON®-TB Gold test.
    Inclusion and exclusion criteria
    Inclusion criteria:
    • Subjects must be 65 to 80 years of age inclusive, at the Screening Visit.
    • Subjects who are healthy, as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring or a subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included if the investigator and the GlaxoSmithKline (GSK) Medical Monitor agree that the finding is unlikely to introduce risk factors and will not interfere with the study procedures and objectives. Additionally, laboratory assessments that are specifically listed in the inclusion or exclusion criteria and are outside of the reference range can be repeated once during the screening period.
    • Body weight >=50 kilograms (kg) and body mass index (BMI) within the range 19
    • 34 kg per meter square (kg/m^2) (inclusive).
    • Male or female subjects will be included. A female subject is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies: Not a woman of childbearing potential (WOCBP) or a WOCBP who agrees to follow the contraceptive guidance during the treatment period and for at least 60 hours after the last dose of study treatment.
    • Capable of giving signed informed consent.
    • AST, ALT, alkaline phosphatase and bilirubin <= 1.5 × upper limit of normal (ULN) (isolated bilirubin > 1.5 × ULN is acceptable if bilirubin is fractionated and direct bilirubin < 35 percent).
    • Resting BP of <= 160/90 millimeters of mercury (mmHg), irrespective of anti-hypertensive medication status for the subject.
    • Able to consume the Food and Drug Administration (FDA) defined high fat meal within 30 minutes in each of the four treatment periods where study treatment is administered in a fed state.
    Exclusion criteria:
    • Significant history of or current cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study treatment; or interfering with the interpretation of data.
    • Evidence of active or latent tuberculosis (TB) as documented by medical history and examination, chest x-rays (posterior anterior and lateral), and TB testing: either a positive tuberculin skin test [TST; defined as a skin induration <5 millimeter (mm) at 48 to 72 hours, regardless of Bacillus Calmette-Guerin (BCG) or other vaccination history] or a positive (not indeterminate) QuantiFERON®-TB Gold test.
    • Lymphoma, leukemia, or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years.
    • Breast cancer within the past 10 years.
    • ALT >1.5x ULN
    • Bilirubin >1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35 percent).
    • Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
    • Corrected QT interval (QTc) >450 milliseconds (msec).
    • Use of prescription or non-prescription drugs, including proton pump inhibitors, histamine receptor 2 antagonists, systemic antacid medications (unless these can be held during the study), vitamins, herbal and dietary supplements (including St John’s Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study treatment until completion of the last study assessment , unless in the opinion of the investigator and GSK Medical Monitor, the medication will not interfere with the study procedures or compromise subject safety. Some examples of exceptions (permitted medications) are: Stable dose of anti-hypertensive medication for at least 3 months prior to the screening visit; Stable dose of lipid-lowering medications (statins or fibrates) for at least 3 months prior to the screening visit; Antacids up to 24 hours prior to dosing.
    • Participation in the study would result in loss of blood or blood products in excess of 500 milliliter (mL) within 3 months.
    • The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 3 months, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
    • Exposure to more than 4 new chemical entities within 12 months prior to the first dosing day.
    • Participation in a previous clinical trial with danirixin within 1 year prior to the first dosing day in the current study.
    • Female Subjects: Positive urine beta-human chorionic gonadotropin (beta-hCG) test at screening.
    • Presence of Hepatitis B surface antigen (HBsAg) at screening Positive Hepatitis C antibody test result at screening.
    • Positive Hepatitis C ribonucleic acid (RNA) test result at screening or within 3 months prior to first dose of study treatment.
    • For potent immunosuppressive agents, presence of the Hepatitis B core antibody (HBcAb) should also lead to exclusion from the study even if HBsAg is negative.
    • Positive pre-study drug/alcohol screen.
    • Positive human immunodeficiency virus (HIV) antibody test.
    • Regular use of known drugs of abuse.
    • Regular alcohol consumption within 6 months prior to the study defined as: an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 grams of alcohol: a half-pint (approximately 240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits.
    • Consumption of red wine, Seville oranges, grapefruit or grapefruit juice and/or pummelos, citrus fruits, grapefruit hybrids or fruit juices from 7 days prior to the first dose of study treatment until collection of the final blood sample.
    • Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 90 days prior to screening.
    • Sensitivity to heparin or heparin-induced thrombocytopenia.
    • Sensitivity to any of the study treatments, or components thereof, or drug or other allergy that, in the opinion of the investigator or medical monitor, contraindicates participation in the study.

    Trial location(s)

    Location
    Status
    Contact us
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    Location
    GSK Investigational Site
    Overland Park, Kansas, United States, 66211
    Status
    Study Complete
    Contact us

    Study documents

    Clinical study report
    Available language(s): English
    Download document(s)
    Protocol
    Available language(s): English
    Download document(s)
    Statistical analysis plan
    Available language(s): English
    Download document(s)

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Results posted on ClinicalTrials.gov

    Recruitment status
    Study complete
    Actual primary completion date
    2018-25-07
    Actual study completion date
    2018-25-07

    Plain language summaries

    Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

    Additional information about the trial

    Additional information
    Not applicable
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