A Study to Evaluate the Safety and Pharmacokinetics of BX-001N in Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

November 17, 2023

Primary Completion Date

November 6, 2024

Study Completion Date

November 6, 2024

Conditions
Ischemia-reperfusion Injury
Interventions
DRUG

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.

DRUG

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.

DRUG

Placebo

Participants will receive matching placebo across Part 1 and 2 of the study.

Trial Locations (1)

5000

CMAX Clinical Research, Adelaide

All Listed Sponsors
lead

Bilix Co.,Ltd.

INDUSTRY

NCT06097702 - A Study to Evaluate the Safety and Pharmacokinetics of BX-001N in Healthy Participants | Biotech Hunter | Biotech Hunter