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NCT01371708 · ClinicalTrials.gov registry record · Phase 3
A 6-Month Extension Study To The B2061032 Study To Evaluate The Safety, Tolerability, And Efficacy Of DVS SR In The Treatment Of Child And Adolescent Outpatients With MDD
A Phase 3 study, sponsored by Pfizer.
- Completed
- Registry status
- Phase 3
- Development phase
- 283
- Enrollment target
NCT01371708: Completed Phase 3 study, sponsored by Pfizer.
NCT01371708 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 283 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01371708, a Phase 3 study, has completed, sponsored by Pfizer.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 283 participants
- Enrollment target
Study Summary
This is a 6-month, open-label, flexible-dose study evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) in the Treatment of Child and Adolescent Outpatients with Major Depressive Disorder (MDD).
Primary Outcome
A TEAE was defined as an event that was absent before treatment and emerged or worsened during the treatment period.
Interventions
- DRUG DVS SR
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 283 participants |
| Start Date | 2012-02-02 |
| Est. Completion | 2016-04-22 |
| Phase | Phase 3 |
What the finished NCT01371708 record still lists
NCT01371708 is an interventional study that assigns participants to a tested intervention. The registered 283 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (63% lower).
The record links to 0 conditions, and to 1 intervention - of which DVS SR is the first listed.
NCT01371708 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01371708 about?
NCT01371708 is a clinical study titled "A 6-Month Extension Study To The B2061032 Study To Evaluate The Safety, Tolerability, And Efficacy Of DVS SR In The Treatment Of Child And Adolescent Outpatients With MDD". This is a 6-month, open-label, flexible-dose study evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) in the Treatment of Child and Adolescent Outpatients with Major Depressive Disorder (MDD).
What is the current status of trial NCT01371708?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 283 participants. The study started on 2012-02-02. Estimated completion is 2016-04-22.
What interventions are being tested in trial NCT01371708?
The interventions under investigation include: DVS SR (DRUG).
Who is sponsoring clinical trial NCT01371708?
This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01371708's enrollment target sits among peer trials
283 1194th of 2000 higher than 807 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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