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NCT02220218 · ClinicalTrials.gov registry record · Phase 1
Bioequivalence Study of Metformin Component of Canagliflozin and Metformin Fixed Dose Combination Immediate Release (IR) Tablet Comparing With Metformin IR Tablet Co-administered With Canagliflozin Tablet in Healthy Fed and Fasted Participants
A Phase 1 study, sponsored by Janssen Research & Development.
- Completed
- Registry status
- Phase 1
- Development phase
- 2
- Enrollment target
NCT02220218: Completed Phase 1 study, sponsored by Janssen Research & Development.
NCT02220218 is a Phase 1 study that has completed, run by Janssen Research & Development. The registered enrollment target is 2 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02220218, a Phase 1 study, has completed, sponsored by Janssen Research & Development.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 2 participants
- Enrollment target
Study Summary
The purpose of this study to evaluate the bioequivalence (is the amount same in both the pills) of metformin component of the canagliflozin and metformin immediate release (IR) fixed dose combination (FDC) tablet compared with the metformin IR tablet co-administered with canagliflozin tablet in healthy fed and fasted participants.
Primary Outcome
Plasma concentrations of metformin are used to evaluate how much metformin is in the blood over time.
Interventions
- DRUG Canagliflozin
- DRUG Metformin IR
- DRUG Canagliflozin + Metformin Immediate Release (IR) Fixed Dose Combination (FDC)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2014-08 |
| Est. Completion | 2014-10 |
| Phase | Phase 1 |
What the finished NCT02220218 record still lists
NCT02220218 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 3 interventions - of which Canagliflozin is the first listed.
NCT02220218 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02220218 about?
NCT02220218 is a clinical study titled "Bioequivalence Study of Metformin Component of Canagliflozin and Metformin Fixed Dose Combination Immediate Release (IR) Tablet Comparing With Metformin IR Tablet Co-administered With Canagliflozin Tablet in Healthy Fed and Fasted Participants". The purpose of this study to evaluate the bioequivalence (is the amount same in both the pills) of metformin component of the canagliflozin and metformin immediate release (IR) fixed dose combination (FDC) tablet compared with the metformin IR tablet co-administered with canagliflozin tablet in heal...
What is the current status of trial NCT02220218?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 2 participants. The study started on 2014-08. Estimated completion is 2014-10.
What interventions are being tested in trial NCT02220218?
The interventions under investigation include: Canagliflozin (DRUG), Metformin IR (DRUG), Canagliflozin + Metformin Immediate Release (IR) Fixed Dose Combination (FDC) (DRUG).
Who is sponsoring clinical trial NCT02220218?
This trial is sponsored by Janssen Research & Development, which has 593 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02220218's enrollment target sits among peer trials
2 2000th of 2000 the lowest 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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