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Clinical Trials/NCT01195675
NCT01195675CompletedPhase 1

Assessment of the Effect of 25 mg and 200 mg of BI 10773 as Single Dose on the QT Interval in Healthy Female and Male Subjects. A Randomised, Placebo Controlled, Double-blind, Five-period Crossover Phase-I-study With Moxifloxacin as Positive Control

Boehringer Ingelheim1 site in 1 country30 target enrollmentStarted: August 2010Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Empa 25mg: Mean QTcN Change From Baseline Between 1 and 4 Hours After Dosing

Study Overview

Brief Summary

The objective of this study is to demonstrate that BI 10773 does not prolong the QT(c) interval more than placebo

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Double

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

BI 10773

Experimental

single oral (high and low) dose per subject

Intervention: BI 10773 (low) (Drug)

BI 10773

Experimental

single oral (high and low) dose per subject

Intervention: BI 10773 (high) (Drug)

Placebo

Placebo Comparator

2 single oral doses per subject

Intervention: BI 10773 Placebo (Drug)

Moxifloxacin

Active Comparator

single oral dose per subject

Intervention: Moxifloxacin (Drug)

Outcomes

Primary Outcomes

Empa 25mg: Mean QTcN Change From Baseline Between 1 and 4 Hours After Dosing

Time Frame: 60 minutes (min), 50min and 40 min before the first dose and 1 hour (h), 1.5h, 2h, 2.5h, 3h and 4h after the first dose

Mean QTcN (heart rate-corrected QT interval, using a study population-based approach) from the ECGs obtained between 1h to 4h following drug administration minus the mean QTcN from the baseline electrocardiogram (ECGs) obtained pre-dose at each visit, for empa 25mg. Note, the treatment means presented are actually adjusted means.

Empa 200mg: Mean QTcN Change From Baseline Between 1 and 4 Hours After Dosing

Time Frame: 60 minutes (min), 50min and 40 min before the first dose and 1 hour (h), 1.5h, 2h, 2.5h, 3h and 4h after the first dose

Mean QTcN (heart rate-corrected QT interval, using a study population-based approach) from the ECGs obtained between 1h to 4h following drug administration minus the mean QTcN from the baseline ECGs obtained pre-dose at each visit, for empa 200mg. Note, the treatment means presented are actually adjusted means.

Secondary Outcomes

  • Empa 25 mg: Mean QTcN Change From Baseline Between 30 Minutes and 24 Hours After Dosing(60 minutes (min), 50min and 40 min before the first dose and 30min, 1 hour (h), 1.5h, 2h, 2.5h, 3h, 4h, 6h, 8h, 12h and 24h after the first dose)
  • Empa 200 mg: Mean QTcN Change From Baseline Between 30 Minutes and 24 Hours After Dosing(60 minutes (min), 50min and 40 min before the first dose and 30min, 1 hour (h), 1.5h, 2h, 2.5h, 3h, 4h, 6h, 8h, 12h and 24h after the first dose)
  • Mean QTcN Change From Baseline Between 2 and 4 Hours After Dosing(60 minutes (min), 50min and 40 min before the first dose and 2 hour (h), 2.5h, 3h and 4h after the first dose)
  • Empa 25mg: Change From Mean Baseline in QTcN at Each Time Point Between 30 Minutes and 24 Hours After Dosings(60 minutes (min), 50min and 40 min before the first dose and 0.5 hour (h), 1h, 1.5h, 2h, 2.5h, 3h, 4h, 6h, 8h, 12h and 24h after the first dose)
  • Empa 200mg: Change From Mean Baseline in QTcN at Each Time Point Between 30 Minutes and 24 Hours After Dosings(60 minutes (min), 50min and 40 min before the first dose and 0.5 hour (h), 1h, 1.5h, 2h, 2.5h, 3h, 4h, 6h, 8h, 12h and 24h after the first dose)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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