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Regulatory Post Marketing Surveillance Study of NovoRapid for New Drug Re-examination

NCT01490112 COMPLETED

This study is conducted in Asia. The aim of this study is to observe the safety and efficacy of insulin aspart (NovoRapid®) administered via vial and three different devices.

Details

Lead sponsorNovo Nordisk A/S
StatusCOMPLETED
Enrolment1239
Start date2005-01
Completion2006-06

Conditions

Interventions

Primary outcomes

Countries

South Korea