drugset / Trial / NCT01783691

Safety, Pharmacokinetic, and Pharmacodynamic Study of NKTT120 in Adult Patients With Stable Sickle Cell Disease (SCD)

NCT01783691 ↗

Phase 1 Completed 21 enrolled NKT Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, pharmacokinetics, and pharmacodynamics of NKTT120 in adult patients with stable sickle cell disease.

Timeline

Start
2013-02
Primary completion
2015-05
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject NKTT120 Monoclonal antibody 0.001 mg/kg Intravenous
Subject NKTT120 Monoclonal antibody 0.1 mg/kg Intravenous
Subject NKTT120 Monoclonal antibody 0.3 mg/kg Intravenous
Subject NKTT120 Monoclonal antibody 1 mg/kg Intravenous

Indications