drugset / Trial / NCT02211261

A Phase 1 Single/Multiple Dose Study Of PF-06293620 To Assess Safety, Tolerability And Pharmacokinetics In Subjects With Type 2 Diabetes Mellitus

NCT02211261 ↗

Phase 1 Completed 84 enrolled Pfizer
RandomizedParallel-groupDouble-blindBasic science

Summary

A first in human study to determine the safety, tolerability and pharmacokinetics of single and multiple ascending doses of PF-06293620 in subjects with Type 2 Diabetes Mellitus

Timeline

Start
2014-09-15
Primary completion
2017-01-27
Completion
2017-01-27

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-06293620 Unknown 0.3 mg/kg Subcutaneous
Subject PF-06293620 Unknown 1 mg/kg Subcutaneous
Subject PF-06293620 Unknown 3 mg/kg Subcutaneous
Subject PF-06293620 Unknown 6 mg/kg Subcutaneous
Subject PF-06293620 Unknown 75 mg Subcutaneous
Subject PF-06293620 Unknown 150 mg Subcutaneous
Subject PF-06293620 Unknown 250 mg Subcutaneous