Last updated: 10/31/2025 15:00:20
Safety, Tolerability and Blood Sampling of GSK3923868 Administered via Dry Powder Inhaler to Healthy Participants of Chinese, Japanese and European Ancestry
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study of the Safety, Tolerability and Pharmacokinetics of Single Doses of GSK3923868 Administered Via Dry Powder Inhaler to Healthy Participants of Chinese, Japanese and European Ancestry
Trial description: This study is designed to understand how the drug GSK3923868 works in the bodies of healthy people from Japanese, Chinese, and European ancestries. This is important to meet the rules for including these groups in future worldwide studies. The study is carefully planned to reduce differences that might come from comparing results across different studies and locations, making it easier to compare results between these ethnic groups. The main goal is to check if GSK3923868 is safe and easy to tolerate when given as a single inhaled dose to healthy people from these three ancestries. The study also wants to see how the drug moves in the blood after a single inhaled dose in these groups. On the first day of the study, participants will be randomly chosen to receive either a single dose of GSK3923868 or a placebo. The aim is to have enough people take part so that 10 healthy people from each ancestry group (a total of 30 people) can successfully finish the study. Should a participant withdraw from the study before completion, the GSK Medical Monitor and the investigator may select a replacement. The replacement participant will be assigned the same treatment as the original participant.
Primary purpose:
Treatment
Trial design:
Parallel
Masking:
Triple (Participant, Care Provider, Investigator)
Allocation:
Randomized
Primary outcomes:
Number of Participants with Adverse events (AE)
Timeframe: Up to Day 14 (End of follow up)
Number of Participants with Serious Adverse events (SAE)
Timeframe: Up to Day 14 (End of follow up)
Number of Participants with Clinically Significant Changes in Laboratory Values
Timeframe: Up to Day 14 (End of follow up)
Number of Participants with Clinically Significant Changes in Laboratory values
Timeframe: Up to Day 14 (End of follow up)
Number of Participants with Clinically Significant Changes in Vital signs
Timeframe: Up to Day 14 (End of follow up)
Number of Participants with Clinically Significant Changes in 12-lead Electrocardiogram (ECG)
Timeframe: Up to Day 14 (End of follow up)
Number of Participants with Clinically Significant Changes in Spirometry Measurements
Timeframe: On Day 14 (End of follow up)
Area Under the Plasma GSK3923868 Concentration Versus Time Curve from Time Zero to Last Quantifiable Concentration (AUC[0-t]) of GSK3923868
Timeframe: Up to Day 4
Area under the Plasma GSK3923868 Concentration versus Time Curve from Time zero to Infinity (AUC[0-inf]) of GSK3923868
Timeframe: Up to Day 4
Maximum Observed GSK3923868 Plasma Concentration (Cmax) of GSK3923868
Timeframe: Up to Day 4
Time to Maximum Observed Plasma Drug Concentration (Tmax) of GSK3923868
Timeframe: Up to Day 4
Terminal Half-life (T1/2) of GSK3923868
Timeframe: Up to Day 4
Secondary outcomes:
Not applicable
Interventions:
Drug: GSK3923868
Drug: Placebo
Enrollment:
30
Observational study model:
Not applicable
Primary completion date:
2024-01-11
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Respiratory Tract Infections
Product
Not applicable
Collaborators
Not applicable
Study date(s)
September 2024 to November 2024
Type
Interventional
Phase
1
Participation criteria
Sex
Female & Male
Age
18 - 50 Years
Accepts healthy volunteers
Yes
- Participants who are generally healthy as determined by medical evaluation based on screening medical history, physical examination, vital signs, electrocardiogram (ECG) assessment, pulmonary function testing and laboratory tests
- Body weight at least 50.0 kilograms (kg) for male participants or at least 45.0 kg for female participants
- History or presence of 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 intervention or interfering with the interpretation of data
- Serum Alanine transaminase (ALT) and Aspartate Aminotransferase (AST) above Upper limit of normal (ULN)
Inclusion and exclusion criteria
Inclusion criteria:
- Participants who are generally healthy as determined by medical evaluation based on screening medical history, physical examination, vital signs, electrocardiogram (ECG) assessment, pulmonary function testing and laboratory tests
- Body weight at least 50.0 kilograms (kg) for male participants or at least 45.0 kg for female participants
- Body Mass Index (BMI) within the range of 18.0–28.0 kilograms per square meter (kg/m^2) (inclusive)
- A female participant is eligible to participate if she is not pregnant or breastfeeding and is a Woman of non-childbearing potential (WONCBP); or Woman of childbearing potential (WOCBP) and using an acceptable contraceptive method; or A WOCBP must have a negative highly sensitive pregnancy test within 30 days before the first dose of study intervention
- Informed consent: Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
- Participants of Chinese ancestry are eligible if they are born in mainland China, Hong Kong or Taiwan; descendant of 4 ethnic Chinese grandparents and 2 ethnic Chinese parents; have lived outside mainland China, Hong Kong or Taiwan for less than 10 years at the time of screening
- Participants of Japanese ancestry are eligible if they are born in Japan, descendent of 4 ethnic Japanese grandparents and 2 ethnic Japanese parents; have lived outside Japan less than 10 years at the time of screening
- Participants of European ancestry are eligible if they self-identified as being European ancestry (that is, from the original people of Europe) irrespective of place of birth and current place of residence; descendent of 4 grandparents and 2 parents of European ancestry
Exclusion criteria:
- History or presence of 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 intervention or interfering with the interpretation of data
- Serum Alanine transaminase (ALT) and Aspartate Aminotransferase (AST) above Upper limit of normal (ULN)
- Total Bilirubin above ULN (isolated bilirubin above ULN is acceptable if total bilirubin is fractionated and direct bilirubin less than [<] 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)
- QTcF greater than (>) 450 milliseconds (msec) at Screening visit based on the average of triplicate ECGs
- Past or intended use of over-the-counter or prescription medication, including 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) before the first dose of study treatment, unless in the opinion of the investigator and the GSK Medical Monitor (if necessary), the medication will not interfere with the study procedures or compromise participant safety
- Recent donation of blood or blood products such that participation in this study would result in loss of blood in excess of 500 mL within a 60-day period.
- Exposure to more than 4 new chemical or molecular entities within 12 months before the first dosing day
- Current enrolment or past participation in a clinical trial and has received an investigational product within the following time period before the first dosing day in this study: 45 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer)
- FEV1 <80% predicted normal value at Screening
- Presence of hepatitis B surface antigen at screening or within 3 months prior to first dose of study intervention
- Positive hepatitis C antibody test result at screening or within 3 months prior to first dose of study intervention
- Positive hepatitis C RNA test result at screening or within 3 months prior to first dose of study intervention
- Positive pre-study drug/alcohol screen
- Positive HIV antibody test
- Current or history of drug abuse
- Current or previous use of tobacco- or nicotine-containing products (e.g. cigarettes, nicotine patches or electronic devices) within 6 months before screening and/or have a smoking pack history of >5 pack years
- Positive urine cotinine test indicative of recent smoking at Screening or admission to the clinical research unit
- History of regular alcohol consumption within 6 months prior to the study defined as: An average weekly intake of >14 units for males and females
- Sensitivity to the study intervention 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)
Study documents
No study documents available.
Results overview
Study Results yet to be posted
Recruitment status
Completed
Actual primary completion date
2024-01-11
Actual study completion date
2024-01-11
Plain language summaries
Summary of results in plain language
Available language(s): English
To view plain language summaries on trialsummaries.com click here.
Additional information about the trial
Additional information
Not applicable
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