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NCT02064907 · ClinicalTrials.gov registry record · Phase 1
Bioavailability, Safety, and Pharmacodynamics of Dexlansoprazole Delayed-Release Orally Disintegrating Tablets in Healthy Participants
A Phase 1 study, sponsored by Takeda.
- Completed
- Registry status
- Phase 1
- Development phase
- 52
- Enrollment target
NCT02064907: Completed Phase 1 study, sponsored by Takeda.
NCT02064907 is a Phase 1 study that has completed, run by Takeda. The registered enrollment target is 52 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02064907, a Phase 1 study, has completed, sponsored by Takeda.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 52 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the pharmacokinetics (PK) and Pharmacodynamics (PD) of dexlansoprazole delayed-release orally disintegrating (OD) tablets administered on the tongue and swallowed without water.
Primary Outcome
Maximum observed plasma concentration (Cmax) is the peak plasma concentration of a drug after administration, obtained directly from the plasma concentration-time curve.
Interventions
- DRUG Dexlansoprazole Delayed Release Orally Disintegrating Tablets
- DRUG Dexlansoprazole Delayed Release Capsules
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2014-02 |
| Est. Completion | 2014-04 |
| Phase | Phase 1 |
What the finished NCT02064907 record still lists
NCT02064907 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% lower).
The record links to 0 conditions, and to 2 interventions - of which Dexlansoprazole Delayed Release Orally Disintegrating Tablets is the first listed.
NCT02064907 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02064907 about?
NCT02064907 is a clinical study titled "Bioavailability, Safety, and Pharmacodynamics of Dexlansoprazole Delayed-Release Orally Disintegrating Tablets in Healthy Participants". The purpose of this study is to assess the pharmacokinetics (PK) and Pharmacodynamics (PD) of dexlansoprazole delayed-release orally disintegrating (OD) tablets administered on the tongue and swallowed without water.
What is the current status of trial NCT02064907?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 52 participants. The study started on 2014-02. Estimated completion is 2014-04.
What interventions are being tested in trial NCT02064907?
The interventions under investigation include: Dexlansoprazole Delayed Release Orally Disintegrating Tablets (DRUG), Dexlansoprazole Delayed Release Capsules (DRUG).
Who is sponsoring clinical trial NCT02064907?
This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02064907's enrollment target sits among peer trials
52 956th of 2000 higher than 1,032 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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