drugset / Trial / NCT02035605

A Phase 1 Study of an Investigational Drug, ALN-AT3SC, in Healthy Volunteers and Hemophilia A or B Patients

NCT02035605

Phase 1 Completed 51 enrolled Sanofi
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to determine the safety, tolerability, and pharmacokinetics of ALN-AT3SC in healthy volunteers and Hemophilia A or B patients.

Timeline

Start
2014-01-20
Primary completion
2017-07-20
Completion
2017-07-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fitusiran Small interfering RNA (siRNA) 0.015 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 0.03 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 0.045 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 0.075 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 0.225 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 0.45 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 0.9 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 1.8 mg/kg Subcutaneous
Comparator Fitusiran Small interfering RNA (siRNA) 80 mg Subcutaneous