drugset / Trial / NCT03446053

A Study to Evaluate the Safety, PK, PD, Immunogenicity of N-Rephasin® SAL200 in Healthy Male Volunteers

NCT03446053 ↗

Phase 1 Completed 33 enrolled Intron Biotechnology, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the safety, pharmacokinetics, pharmacodynamics and immunogenicity of N-Rephasin® SAL200 following single and multiple ascending doses in healthy male volunteers after continuous intravenous infusion over 60 minutes.

Timeline

Start
2018-02-07
Primary completion
2019-02-07
Completion
2019-02-07

Drugs

EvaluationDrugModalityDoseRoute
Subject N-Rephasin® SAL200 Unknown 3 mg/kg Intravenous
Subject N-Rephasin® SAL200 Unknown 6 mg/kg Intravenous
Subject N-Rephasin® SAL200 Unknown 9 mg/kg Intravenous
Subject N-Rephasin® SAL200 Unknown 12 mg/kg Intravenous