drugset / Trial / NCT06170827

Study to Evaluate the AIO-001 in Healthy Participants

NCT06170827 ↗

Phase 1 Completed 16 enrolled Syneos Health Aiolos Bio, Inc. · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This goal of the open-label single dose study is to evaluate and compare the safety, tolerability, pharmacokinetic (PK), and immunogenicity of AIO-001 using two different formulations in 16 healthy volunteers.

Timeline

Start
2023-11-21
Primary completion
2024-07-15
Completion
2024-07-15

Drugs

EvaluationDrugModalityDoseRoute
Subject AIO-001 Unknown 400 mg Subcutaneous