drugset / Trial / NCT05991661

XKH001 Injection in Healthy Subjects

NCT05991661 ↗

Phase 1/2 Completed 24 enrolled Beijing Kanova Biopharmaceutical Co., LTD
RandomizedParallel-groupDouble-blindHealth-services research

Summary

This study is a randomized, double-blind, placebo-controlled, multiple ascending dose (MAD) clinical study. The primary objective is to evaluate the safety, tolerability, and PK of multiple SC doses of XKH001 in healthy subjects.

Timeline

Start
2023-05-12
Primary completion
2024-02-20
Completion
2024-03-29

Drugs

EvaluationDrugModalityDoseRoute
Comparator XKH001 Monoclonal antibody 100 mg Subcutaneous
Comparator XKH001 Monoclonal antibody 300 mg Subcutaneous
Comparator XKH001 Monoclonal antibody 600 mg Subcutaneous

Indications