drugset / Trial / NCT06577428

A Study of RAY1225 at Different Injection Sites in Participants With Different Body Sizes

NCT06577428

Phase 1 Completed 48 enrolled Guangdong Raynovent Biotech Co., Ltd
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to compare the amount of RAY1225 that gets into the blood stream and how long it takes the body to get rid of it, when injected under the skin of the upper arm and thigh compared to the abdomen. The study will be conducted in healthy males and females with different body sizes. The tolerability of RAY1225 will be evaluated and information about any side effects experienced will be collected. For each participant, the study will last about 7 weeks, including screening.

Timeline

Start
2024-07-30
Primary completion
2024-09-29
Completion
2024-10-08

Drugs

EvaluationDrugModalityDoseRoute
Subject RAY1225 Unknown 3 mg Subcutaneous

Indications

No indication recorded.