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NCT02720198 · ClinicalTrials.gov registry record · Phase 3

Levomilnacipran ER vs. Adjunctive Quetiapine for Adults With Inadequate Relief With SSRIs in MDD

A Phase 3 study, sponsored by Duke University.

Completed
Registry status
Phase 3
Development phase
60
Enrollment target

NCT02720198: Completed Phase 3 study, sponsored by Duke University.

NCT02720198 is a Phase 3 study that has completed, run by Duke University. The registered enrollment target is 60 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02720198, a Phase 3 study, has completed, sponsored by Duke University.

COMPLETED
Registry status
Phase 3
Development phase
60 participants
Enrollment target

Study Summary

This study's primary objective is to compare the efficacy and tolerability of switching patients with inadequate relief on generic SSRIs to levomilnacipran versus adding a new treatment (quetiapine) to the participants' existing treatment with people diagnosed with depression (major depression disorder). The secondary objective is to examine the response and remission rates following the switch from a generic SSRI to levomilnacipran ER and augmentation with quetiapine along with examining changes in neurocognitive and apathy measures after the switch.

Primary Outcome

A ten-item diagnostic questionnaire used to measure the severity of depressive episodes in patients with mood disorders. Total scores will range from 0 to 60. Higher scores indicate greater severity of depressive episodes.

Interventions

  • DRUG Quetiapine
  • DRUG Levomilnacipran

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2017-01-23
Est. Completion 2018-06-12
Phase Phase 3
Duke University

1,725 total trials

What the finished NCT02720198 record still lists

NCT02720198 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Quetiapine is the first listed.

NCT02720198 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02720198 about?

NCT02720198 is a clinical study titled "Levomilnacipran ER vs. Adjunctive Quetiapine for Adults With Inadequate Relief With SSRIs in MDD". This study's primary objective is to compare the efficacy and tolerability of switching patients with inadequate relief on generic SSRIs to levomilnacipran versus adding a new treatment (quetiapine) to the participants' existing treatment with people diagnosed with depression (major depression disor...

What is the current status of trial NCT02720198?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 60 participants. The study started on 2017-01-23. Estimated completion is 2018-06-12.

What interventions are being tested in trial NCT02720198?

The interventions under investigation include: Quetiapine (DRUG), Levomilnacipran (DRUG).

Who is sponsoring clinical trial NCT02720198?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02720198's enrollment target sits among peer trials

60 1804th of 2000 higher than 177 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT02720198, the US trial registry maintained by the National Library of Medicine. NCT02720198 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.