drugset / Trial / NCT01908894

Pharmacokinetic and Pharmacodynamic Properties of BIOD-123 and BIOD-125 Compared to Humalog® in Subjects With Type 1 Diabetes Including Assessments of Injection Site Toleration

NCT01908894

Phase 1 Completed 12 enrolled Biodel
RandomizedCrossoverDouble-blindTreatment

Summary

The primary objective is to assess the speed of absorption of BIOD-123 and BIOD-125 and compare them to Humalog.

Timeline

Start
2012-02
Primary completion
2012-03
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BIOD-123 Unknown 0.2 iu/kg Subcutaneous
Subject BIOD-125 Unknown 0.2 iu/kg Subcutaneous
Comparator Insulin Lispro Protein / enzyme biologic 0.2 iu/kg Subcutaneous

Indications