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Evaluating the Safety and Effectiveness of Liraglutide in Subjects With Type 2 Diabetes

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Novo Nordisk

Status

Completed

Conditions

Diabetes
Diabetes Mellitus, Type 2

Treatments

Drug: liraglutide

Study type

Observational

Funder types

Industry

Identifiers

NCT01403025
U1111-1120-7575 (Other Identifier)
NN2211-3772
JapicCTI-111559 (Registry Identifier)

Details and patient eligibility

About

This trial is conducted in Asia. The aim of the trial is to assess the incidence rate and type of SADRs (serious adverse drug reactions).

Enrollment

4,121 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects with type 2 diabetes mellitus, including newly-diagnosed subjects, who require treatment with liraglutide

Exclusion criteria

  • Subjects who are or have previously been on liraglutide
  • Subjects who have previously been enrolled in the study
  • Subjects with a hypersensitivity to liraglutide 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 cancer (except basal cell skin cancer or squamous cell skin cancer) or any clinically significant disorder, except for conditions associated with type 2 diabetes mellitus history which in the physicians' opinion could interfere with the results of the trial
  • Known or suspected abuse of alcohol or narcotics

Trial design

4,121 participants in 1 patient group

Liraglutide
Treatment:
Drug: liraglutide

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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