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An Observational Study of Type 2 Diabetes in Patients Starting on NovoMix® 30 Treatment

Novo Nordisk logo

Novo Nordisk

Status

Completed

Conditions

Diabetes
Diabetes Mellitus, Type 2

Treatments

Drug: biphasic insulin aspart 30

Study type

Observational

Funder types

Industry

Identifiers

NCT00696995
BIASP-1917

Details and patient eligibility

About

This study is conducted in Europe. The aim of this observational study is to evaluate the incidence of serious adverse drug reactions when initiating or switching to insulin therapy with NovoMix® 30 in subjects with type 2 diabetes under normal clinical practice conditions

Enrollment

509 patients

Sex

All

Ages

Under 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with Type 2 diabetes
  • Insulin-naive or previously treated by basal only insulin therapy

Exclusion criteria

  • Patients who are unlikely to comply with the protocol
  • Pregnancy or breastfeeding or intention of becoming pregnant

Trial design

509 participants in 1 patient group

A
Treatment:
Drug: biphasic insulin aspart 30

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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