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Clinical Trials/PER-014-03
PER-014-03
Completed
Phase 1

A MULTICIENTRIC, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY AND EFFICACY OF MK-0767 TO PATIENTS WITH TYPE 2 DIABETES THAT PRESENT INACCURATE GLYCEMIC CONTROL IN THE COMBINED THERAPY OF METFORMIN AND SULFONILUREA.

MERCK SHARP & DOHME PERU S.R.L.,0 sites0 target enrollmentMarch 12, 2003

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
MERCK SHARP & DOHME PERU S.R.L.,
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 12, 2003
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
MERCK SHARP & DOHME PERU S.R.L.,

Eligibility Criteria

Inclusion Criteria

  • Age\> 21 and \<78 years.
  • In stable doses of metformin and sulfonylurea for at least 2
  • weeks before Visit 2 / Week \-6\.
  • Understanding of study procedures and agreement of
  • participate in the study through informed consent

Exclusion Criteria

  • Patients with a history of type 1 diabetes mellitus and / or history
  • of ketoacidosis and / or C\-peptide \<0\.8 ng / mL (\<0\.26 nmol / L).
  • Patients with the following treatments for diabetes during the
  • 8 weeks prior to Visit 1\.
  • Patients with a history of allergy, intolerance or hypersensitivity to troglitazone, rosiglitazone, pioglitazone or other PPAR\-agonists and including a history of elevated liver function test, jaundice, or hepatotoxicity associated with these treatments.

Outcomes

Primary Outcomes

Not specified

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