Clinical Trials Logo

Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled phase I study to evaluate the safety, tolerability, PK profiles and PD effect of single and multiple ascending doses of subcutaneously administered RBD5044 in healthy subjects. The study will be performed in 2 phases: single ascending dose (SAD) phase and multiple ascending doses (MAD) phase in healthy subjects. There are 6 cohorts in SAD phases, the dose levels are 5mg, 20mg, 60mg, 90mg, 120mg and 150mg. There are 3 cohorts in MAD phases, the dose levels are 60mg, 90mg and 120mg.The decision to escalate to subsequent dose levels will be made by the SRC based on the review of all available safety information, including AEs, ECGs, vital signs, and clinical laboratory test results in each cohort.


Clinical Trial Description

n/a


Study Design


NCT number NCT05539651
Study type Interventional
Source Suzhou Ribo Life Science Co. Ltd.
Contact Richard Friend, Dr.
Phone +61 403 415 925
Email r.Friend@nucleusnetwork.com.au
Status Recruiting
Phase Phase 1
Start date November 10, 2022
Completion date October 2024