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Clinical Trial Summary

This is a randomized, double-blind, single-dose, parallel two-arm study to compare the pharmacokinetics, safety, and immunogenicity of BAT1706 Injection from different manufacturing batches (by new process and old process) in healthy male subjects.


Clinical Trial Description

A total of 38 subjects are planned to be enrolled and randomized in a 1: 1 ratio to receive a single intravenous drip of BAT1706 Injection (by old process) or BAT1706 Injection (by new process) at 1 mg/kg body weight. A 7-day screening period will be set up for this study. Subjects will be admitted to the hospital 1 day pre-dose (Day -1) and discharged after completing relevant observations and assessments 24 h post-dose. After discharge, subjects should return to the hospital for 12 follow-up visits according to the requirements of this study, on Days 3, 4, 5, 8, 11, 15, 22, 29, 36, 43, 57 and 71 post-dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05865574
Study type Interventional
Source Bio-Thera Solutions
Contact Wenting Li
Phone 15812648239
Email wtli1@bio-thera.com
Status Not yet recruiting
Phase Phase 1
Start date June 2023
Completion date January 2024

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