This study aims to assess the ethnic sensitivity of GSK3862995B in terms of safety, tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) in healthy participants of Chinese, Japanese, and European ancestry to enable the inclusion of Chinese and Japanese participants in future global studies.
Age range
18 Years – 50 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of Participants with Adverse Events (AE)
Timeframe: Up to Week 44 (End of follow up visit)
Number of Participants with Serious Adverse Events (SAE)
Timeframe: Up to Week 44 (End of follow up visit)
Number of Participants with Clinically Significant Changes in Clinical Laboratory Values
Timeframe: Up to Week 36
Number of Participants with Clinically Significant Changes in Vital Signs
Timeframe: Up to Week 36
Number of Participants with Clinically Significant Changes in 12-lead (Electrocardiogram (ECG)
Timeframe: Up to Week 36
Area Under the Serum Concentration-time Curve Extrapolated to Infinity (AUC[0-inf]) of GSK3862995B
Timeframe: Up to Week 36
Maximum Observed Concentration (Cmax) of GSK3862995B
Timeframe: Up to Week 36