Study of Saxagliptin, 5-Hydroxy Saxagliptin, and Metformin concentrations/levels in Pediatric Subjects with T2DM

Study identifier:CV181-153

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Terminated/Withdrawn

Official Title

Evaluation of the Pharmacokinetics of Saxagliptin, 5-Hydroxy Saxagliptin, and Metformin in Children and Adolescents Aged 10 to 17 Years with Type 2 Diabetes Mellitus Following Oral Administration of Saxagliptin and Metformin XR Fixed Dose Combination Tablet and Co-Administration of Saxagliptin and Glucophage® (Metformin) IR Tablets

Medical condition

Type 2 Diabetes Mellitus

Phase

Phase 1

Healthy volunteers

No

Study drug

Metformin immediate release (IR), Saxagliptin, Metformin IR, Saxagliptin/Metformin XR FDC, Metformin XR

Sex

All

Actual Enrollment

4

Study type

Interventional

Age

10 Years - 17 Years

Date

Study Start Date: 01 Sept 2012
Primary Completion Date: 01 Jun 2013
Study Completion Date: 01 Jun 2013

Study design

Allocation: N/A
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Other

Verification:

Verified 01 Jul 2015 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

Astra Zeneca

Inclusion and exclusion criteria