A multicenter, double-blind, randomized, active controlled study to compare the effect of long term treatment with LAF237 50 mg bid to gliclazide up to 320 mg daily in drug naïve patients with type 2 diabetes

Registry ID
EUCTR2004-000540-24
Source registry
EUCTR
Status
Completed
Phase
PHASE3
Sponsor
Novartis Pharma Services AG
Start date
2004-12-14
Completion date
2008-03-03
Last update
2026-08-16

Conditions

Summary

Primary objective 1. To demonstrate the efficacy of LAF237 in patients with type 2 diabetes by testing the hypothesis that the HbA1c reduction with LAF237 is not inferior to that with gliclazide after 104 weeks of treatment.

Locations

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