drugset / Trial / NCT04540770

A Phase 1 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Immunogenicity of HuL001

NCT04540770

Phase 1 Completed 24 enrolled HuniLife Biotechnology, Inc.
RandomizedSequentialTriple-blindTreatment

Summary

This is a first-in-human, two-part, Phase 1 study that will characterize the safety, tolerability, PK, and immunogenicity of HuL001.

Timeline

Start
2021-08-31
Primary completion
2022-03-04
Completion
2024-01-19

Drugs

EvaluationDrugModalityDoseRoute
Subject HuL001 Monoclonal antibody 1 mg/kg
Subject HuL001 Monoclonal antibody 3 mg/kg
Subject HuL001 Monoclonal antibody 5 mg/kg