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NCT02000700 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of Canagliflozin in Older Children and Adolescents With Type 2 Diabetes Mellitus

A Phase 1 study, sponsored by Janssen Research & Development.

Completed
Registry status
Phase 1
Development phase
17
Enrollment target

NCT02000700: Completed Phase 1 study, sponsored by Janssen Research & Development.

NCT02000700 is a Phase 1 study that has completed, run by Janssen Research & Development. The registered enrollment target is 17 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02000700, a Phase 1 study, has completed, sponsored by Janssen Research & Development.

COMPLETED
Registry status
Phase 1
Development phase
17 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the pharmacokinetics (blood levels) and pharmacodynamics (the action or effects a drug has on the body) of canagliflozin in children and adolescents with type 2 diabetes mellitus aged 10 to 17 years (inclusive). Other purposes are to investigate safety and assess the ease of swallowing the tablets.

Primary Outcome

Plasma concentrations of canagliflozin are used to evaluate how long canagliflozin stays in the body.

Interventions

  • DRUG Placebo
  • DRUG Canagliflozin 100 mg
  • DRUG Canagliflozin 300 mg
  • DRUG Canagliflozin 50 mg

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2014-03
Est. Completion 2016-04
Phase Phase 1
Janssen Research & Development

593 total trials

What the finished NCT02000700 record still lists

NCT02000700 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02000700 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02000700 about?

NCT02000700 is a clinical study titled "A Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of Canagliflozin in Older Children and Adolescents With Type 2 Diabetes Mellitus". The purpose of this study is to evaluate the pharmacokinetics (blood levels) and pharmacodynamics (the action or effects a drug has on the body) of canagliflozin in children and adolescents with type 2 diabetes mellitus aged 10 to 17 years (inclusive). Other purposes are to investigate safety and as...

What is the current status of trial NCT02000700?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2014-03. Estimated completion is 2016-04.

What interventions are being tested in trial NCT02000700?

The interventions under investigation include: Placebo (DRUG), Canagliflozin 100 mg (DRUG), Canagliflozin 300 mg (DRUG), Canagliflozin 50 mg (DRUG).

Who is sponsoring clinical trial NCT02000700?

This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02000700's enrollment target sits among peer trials

17 1785th of 2000 higher than 215 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02000700, the US trial registry maintained by the National Library of Medicine. NCT02000700 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.