drugset / Trial / NCT05480579

A Study of IBI311 in Healthy Volunteers

NCT05480579

Phase 1 Completed 28 enrolled Innovent Biologics (Suzhou) Co. Ltd.
RandomizedSequentialDouble-blindTreatment

Summary

It is designed for Multi-center, double-masked, randomized, placebo- control study with dose escalation phase I trial to evaluate the safety, tolerability, PK and immunogenicity profiles of a single intravenous injection of IBI311 in healthy volunteers.

Timeline

Start
2022-08-10
Primary completion
2022-11-23
Completion
2023-01-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Teprotumumab Monoclonal antibody Intravenous

Indications

No indication recorded.