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Investigating the Safety Profile of Liraglutide Under Normal Conditions of Use in Korean Subjects With Type 2 Diabetes Mellitus

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Novo Nordisk

Status

Completed

Conditions

Diabetes
Diabetes Mellitus, Type 2

Treatments

Drug: liraglutide

Study type

Observational

Funder types

Industry

Identifiers

NCT01821846
NN2211-3929
U1111-1132-2221 (Other Identifier)

Details and patient eligibility

About

This trial is conducted in Asia. The aim of this study is to investigate the safety profile of liraglutide (Victoza®) under normal conditions of use in Korean subjects with type 2 diabetes mellitus.

Enrollment

64 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects with T2DM (Type 2 Diabetes Mellitus), including newly-diagnosed subjects, who require treatment with Victoza® according to the clinical judgment of their treating physician
  • Subjects (and/or parents or the subject's legally acceptable representative) who are capable of giving study-specific signed informed consent before any collection of information

Exclusion criteria

  • Subjects with a hypersensitivity to Victoza® or to any of the excipients
  • Subjects who are pregnant, breast feeding or have the intention of becoming pregnant within the study periods
  • Subjects with personal or family history of medullary thyroid carcinoma (MTC)
  • Subjects with multiple endocrine neoplasia syndrome type 2 (MEN2)

Trial design

64 participants in 1 patient group

Liraglutide
Treatment:
Drug: liraglutide

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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