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NCT00799448

Comparison of Efficacy and Safety of Repaglinide Combined With Insulin NPH Versus Biphasic Human Insulin 30 Alone in Inadequately Controlled Subjects With Type 2 Diabetes

Terminated Phase 4 Last updated 20 February 2017
What this trial tests

Phase 4 trial testing repaglinide in Diabetes in 40 participants. Terminated before completion.

Timeline
16 September 2003
Primary endpoint
20 September 2004
20 September 2004

Quick facts

Lead sponsorNovo Nordisk A/S
PhasePhase 4
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment40
Start date16 September 2003
Primary completion20 September 2004
Estimated completion20 September 2004
Sites1 location across Greece

Drugs / interventions tested

Conditions studied

Sponsor

Novo Nordisk A/S — full company profile →

Who can join

Adults 40 to 75, any sex, with Diabetes or Diabetes Mellitus, Type 2. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This trial is conducted in Europe. The aim of this trial is to compare the efficacy and safety of repaglinide combined with insulin NPH versus biphasic human insulin 30 alone in type 2 diabetics inadequately controlled with sulfonylurea (SU) +/ biguanide therapy

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of repaglinide

Trials testing the same drug.

Other recruiting trials for Diabetes

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Other Novo Nordisk A/S trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00799448.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing