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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT00240383

NCT00240383
Completed Phase 3 🇦🇺 Australian site

Who may be able to join

Who might be able to join this trial:

  • You are between 18 and 70 years old (male or female)
  • You have been diagnosed with Type 2 diabetes
  • Your HbA1c blood sugar level (a measure of average blood sugar over time) was between 7.0% and 10.0% at your screening appointment

Who may not be able to join:

  • You have severe diabetes symptoms, such as excessive thirst and frequent urination, along with losing more than 10% of your body weight in the last three months
  • You have taken blood sugar-lowering medications (other than a specific type called thiazolidinediones) for more than three days in a row, or more than seven days total, in the four weeks before screening
  • You have taken a type of diabetes medication called thiazolidinediones for more than three days in a row, or more than seven days total, in the six weeks before screening

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.

Trial details

Status
Completed
Phase
Phase 3
Sponsor
Bristol-Myers Squibb
Registry
clinicaltrials_gov
Start date
1 May 2002
Est. completion
1 June 2006

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇧🇷 Brazil 🇨🇦 Canada 🇨🇿 Czechia 🇫🇷 France 🇮🇹 Italy 🇲🇽 Mexico 🇳🇱 Netherlands 🇵🇱 Poland Puerto Rico 🇿🇦 South Africa 🇪🇸 Spain 🇸🇪 Sweden 🇬🇧 United Kingdom 🇺🇸 United States

7 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

To compare, after 24 weeks of oral administration of double-blind treatment, the change from baseline in hemoglobin A1c (HbA1c) achieved with the highest dose and subsequent doses of BMS-298585 versus the lowest dose of BMS-298585 in subjects with Type 2

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov