A Study to Evaluate the Relative Bioavailability of Two Different Pimicotinib Capsules in Healthy Subjects

Inclusion criteria

• Healthy subjects aged 18 to 50 years (inclusive) at screening;
• Weight ≥ 50.0 kg (male) or ≥ 45.0 kg (female);
• Normal or abnormal but not clinically significant results in medical history, physical examination, clinical laboratory tests and other relevant examinations as assessed by the investigator at Screening;
• Male or female subjects of childbearing potential must agree to use effective methods of contraception during the study and within 6 months after the last dose of investigational product;
• Willing to participate in this study, understand the study procedures and sign the informed consent form prior to screening; willing to comply with the study procedures.

Exclusion criteria

• Past or current medical history of chronic or severe conditions in cardiovascular, respiratory, blood, liver, kidney, gastrointestinal, endocrine or nervous systems;
• Known or persistent mental disorders;
• Past history of gastric or intestinal surgery, or other operations;
• Dysphagia and inability to take the investigational product orally;
• Intolerant to venipuncture, difficult to collect blood samples, and fear of needle sickness and blood;
• Known allergy to two or more kinds of foods and drugs; or allergic to pimicotinib or its excipients;
• History of infection within 30 days prior to screening;
• Symptoms of fatigue and pyrexia within 2 weeks prior to screening;
• Abnormal laboratory tests;
• Positive result for either of the following tests: serum Hepatitis B Surface Antigen (HBsAg), Hepatitis C Virus (HCV) antibody, Human Immunodeficiency Virus (HIV) antibody, and treponema pallidum antibody;
• Participated in any clinical studies of drugs as a study subject and received the study drug within 3 months prior to screening;
• Previously participated in any other study related to pimicotinib and received pimicotinib;
• Used strong inhibitors or inducers of CYP3A4 within 14 days prior to screening and at Screening or intending to use during the study;
• Have special diet requirements and cannot accept to take a unified dietary;
• Consumption of more than 14 units of alcohol per week within 3 months prior to signing the informed consent form, or a positive result for alcohol breath test on the day pre-dose, or unable to abstain from alcohol during the study;
• Consumption of more than 5 cigarettes per day within 3 months prior to signing the informed consent form, or unable to abstain from tobacco products during the study;
• Previous chronic consumption of excessive amount of tea, coffee, or caffeinated beverages or unable to abstain from caffeinated beverages during the study;
• Known history of drug abuse or positive for drug abuse screening test;
• Used over the counter or prescription drugs within 14 days prior to screening, or plan to use such drugs during the study;
• Donated or lost > 400 mL of blood within 3 months prior to screening; received blood transfusions or used blood products within 2 months prior to screening;
• Received vaccine within 2 months prior to screening, or plan to get vaccinated during the study;
• Significant abnormalities and judged by the investigator as clinical significance in vital signs;
• Heart rate-corrected QT interval prolongation;
• Subjects involved in the design or conduct of this study and their immediate family members;
• Subjects who, in the opinion of the investigator, are not suitable for enrollment or may not be able to complete the study for other reasons.