51
Participants
Start Date
November 17, 2023
Primary Completion Date
November 6, 2024
Study Completion Date
November 6, 2024
BX-001N Part 1
Dosage form- IV bolus Dosage- In the five cohorts, each participant receives a single IV bolus administration in one of the five doses based on body weight and followed up for 7 days.
BX-001N Part 2
Dosage form- IV bolus Dosage- In the three cohorts, each participant receives a single IV bolus administration for 4 sequential days in one of the three doses based on body weight and followed up for 14 days.
Placebo
Participants will receive matching placebo across Part 1 and 2 of the study.
CMAX Clinical Research, Adelaide
Bilix Co.,Ltd.
INDUSTRY