drugset / Trial / NCT02170311

Pharmacokinetics, Pharmacodynamics and Safety Study of Z-213 to Iron Deficiency Anemia

NCT02170311 ↗

Phase 1 Completed 24 enrolled Zeria Pharmaceutical
RandomizedSingle-groupOpen-labelTreatment

Summary

The safety, tolerability, pharmacokinetics and pharmacodynamics of Z-213 will be investigated in patients with iron-deficiency anemia after administration of a single dose (100 mg, 500 mg, 800 mg or 1,000 mg iron).

Timeline

Start
2014-06
Primary completion
2015-02
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Z-213 Unknown 100 mg Intravenous
Subject Z-213 Unknown 500 mg Intravenous
Subject Z-213 Unknown 800 mg Intravenous
Subject Z-213 Unknown 1000 mg Intravenous