drugset / Trial / NCT00751842

A Phase III Study to Investigate the Impact of Diamyd in Patients Newly Diagnosed With Type 1 Diabetes (USA)- DIAPREVENT

NCT00751842 ↗

Phase 3 Terminated 331 enrolled Diamyd Therapeutics AB
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The intended purpose of this study was to determine whether Diamyd (rhGAD65 formulated in alum) is effective in preserving the body's own insulin producing capacity in patients recently diagnosed with type 1 diabetes. Based on results from other clinical trials with the study drug it was judged unlikely this study would meet the intended primary or secondary efficacy endpoints. Therefore the primary focus of this study was changed to ensure that safety data was available for at least 6 months following the last dose of active study drug. Thereafter the study was terminated.

Timeline

Start
2008-09
Primary completion
2012-03
Completion
2012-07

Outcome

Outcome not reported

Stopped: “Based on other clinical trial results it was unlikely the study would meet the efficacy endpoints”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator rhGAD65 Vaccine 20 ug Subcutaneous