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NCT02209597 · ClinicalTrials.gov registry record · Phase 4

Clinical Study of Generic and Brand Bupropion in Depression

A Phase 4 study, sponsored by Washington University School of Medicine.

Completed
Registry status
Phase 4
Development phase
74
Enrollment target

NCT02209597: Completed Phase 4 study, sponsored by Washington University School of Medicine.

NCT02209597 is a Phase 4 study that has completed, run by Washington University School of Medicine. The registered enrollment target is 74 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02209597, a Phase 4 study, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
Phase 4
Development phase
74 participants
Enrollment target

Study Summary

Determine bioequivalence between branded and generic bupropion extended release (XL) products (and between generic products) at steady state in patients with major depressive disorder.

Primary Outcome

Area under the curve (AUC) generic/Area under the curve (AUC) brand bupropion

Interventions

  • DRUG Bupropion XL 300

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2014-06-25
Est. Completion 2016-08-14
Phase Phase 4

What the finished NCT02209597 record still lists

NCT02209597 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 1 intervention - of which Bupropion XL 300 is the first listed.

NCT02209597 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02209597 about?

NCT02209597 is a clinical study titled "Clinical Study of Generic and Brand Bupropion in Depression". Determine bioequivalence between branded and generic bupropion extended release (XL) products (and between generic products) at steady state in patients with major depressive disorder.

What is the current status of trial NCT02209597?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 74 participants. The study started on 2014-06-25. Estimated completion is 2016-08-14.

What interventions are being tested in trial NCT02209597?

The interventions under investigation include: Bupropion XL 300 (DRUG).

Who is sponsoring clinical trial NCT02209597?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02209597's enrollment target sits among peer trials

74 1027th of 2000 higher than 968 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT02209597, the US trial registry maintained by the National Library of Medicine. NCT02209597 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.