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NCT07820891
A Trial in Healthy Participants to Assess Drug Interaction Potential of BGB-43395
Conditions: Healthy Adult Participants
Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: Yes
Phase: PHASE1
Enrollment: 24
Sponsor: BeOne Medicines
Location: Fortrea CRU Dallas Texas
Summary
This study will enroll healthy participants to evaluate whether BGB-43395 interacts with other drugs, including midazolam, celecoxib, dabigatran, and rosuvastatin.
Eligibility Criteria
Inclusion Criteria:
* Body mass index between 18.0 and 32.0 kg/m\^2, inclusive.
* In good health, as determined by no clinically significant findings from medical history, 12-lead electrocardiogram and vital signs measurements, and clinical laboratory assessments.
* Participants must not be pregnant or lactating and must agree to use contraception.
Exclusion Criteria:
* Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder, as determined by the investigator
* History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs
* Confirmed systolic blood pressure \>140 or \90 or \100 or \
Source: ClinicalTrials.gov (NCT07820891). StuddyBuddy aggregates publicly available trial information.