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Long-term Daily Use of Trazenta® Tablets in Patients With Type 2 Diabetes Mellitus

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Diabetes Mellitus, Type 2

Treatments

Drug: Trazenta
Drug: OAD

Study type

Observational

Funder types

Industry

Identifiers

NCT01650259
1218.95

Details and patient eligibility

About

Study to investigate the safety and efficacy of long-term daily use of Trazenta® Tablets as monotherapy in patients with type 2 diabetes mellitus and to assess baseline characteristics of patients with type 2 diabetes mellitus starting Trazenta® Tablets or any other oral antidiabetic monotherapy (naïve or switched from prior therapy of different oral antidiabetic drug).

Enrollment

4,876 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and female patients with type 2 Diabetes Mellitus who have never been treated with Trazenta tablets / Linagliptin (monotherapy) before enrollment. (Trazenta group)
  • Patients with type 2 Diabetes Mellitus starting any other oral antidiabetic monotherapy (naïve or switched from prior therapy of different oral antidiabetic drug (OAD)) except Trazenta tablets. (OAD group)

Exclusion criteria

None

Trial design

4,876 participants in 2 patient groups

Oral antidiabetic drug (OAD)
Treatment:
Drug: OAD
Trazenta
Treatment:
Drug: Trazenta

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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