A study to assess the bioequivalence of fixed dose combination of dapagliflozin/metformin XR relative to co-administration of the individual components in healthy Chinese subjects.

Study identifier:D1691C00011

ClinicalTrials.gov identifier:NCT04856007

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Single-centre, Parallel-cohort, Randomized, Open-label, Two-period, Cross-over, Bioequivalence Study of the Fixed Dose Combination of Dapagliflozin/Metformin XR Relative to Co-administration of the Individual Components in Two Cohorts of Healthy Chinese Subjects in the Fed State.

Medical condition

Healthy Volunteer

Phase

Phase 1

Healthy volunteers

Yes

Study drug

Dapagliflozin/metformin XR FDC 5/500 mg, Dapagliflozin/metformin XR FDC 10/1000 mg, Dapagliflozin 5 mg + Metformin 500 mg XR, Dapagliflozin 10 mg + Metformin 1000 mg XR

Sex

All

Actual Enrollment

80

Study type

Interventional

Age

18 Years - 55 Years

Date

Study Start Date: 12 Apr 2021
Primary Completion Date: 14 Jun 2021
Study Completion Date: 14 Jun 2021

Study design

Allocation: Randomized
Endpoint Classification: -
Intervention Model: Crossover Assignment
Masking: -
Primary Purpose: Other

Verification:

Verified 01 Jun 2022 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria