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LAPAS Study: Insulin Glargine in Type 2 Diabetes Mellitus

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Sanofi

Status

Completed

Conditions

Diabetes Mellitus, Type 2

Treatments

Drug: Insulin glargine (LANTUS)

Study type

Observational

Funder types

Industry

Identifiers

NCT00423215
HOE901_5062

Details and patient eligibility

About

The objective of this protocol is to confirm the efficacy and safety profile of Lantus in every day medical practice, in type 2 diabetic patients, have been treated with any other insulin but who did not reach the target of A1c = 7%.

Enrollment

1,007 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with type 2 diabetes mellitus,
  • Having been treated with any other insulin, but who did not reach the target of A1c=7%.
  • Ability and willingness to perform Self Monitoring Blood Glucose measurement

Exclusion criteria

  • Will follow the prescribing information (Summary of Product Characteristics).

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Trial design

1,007 participants in 1 patient group

Patients with Type II diabetes
Treatment:
Drug: Insulin glargine (LANTUS)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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