AzTrials
AzTrials

DepressionPhase 3NCT00406640

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women

A Phase 3 study testing Desvenlafaxine succinate sustained-release (DVS SR) and Escitalopram in people with Depression and Depressive Disorder, run by Wyeth is now a wholly owned subsidiary of Pfizer at 70 sites in 6 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Desvenlafaxine succinate (DVS) is a potent and selective serotonin and norepinephrine reuptake inhibitor (SNRI). This study will investigate the safety, efficacy, and tolerability of DVS SR versus escitalopram in women with major depressive disorder (MDD) who are postmenopausal. Read more about this study

Who is it for?
Ages 40 to 70 years, women only
What is being tested?
Desvenlafaxine succinate sustained-release (DVS SR) and Escitalopram
Could I receive a placebo?
No, everyone receives an active treatment
How many people
595 participants
Where
70 sitesin 6 countries
Study dates
Dec 2006to Oct 2008
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 70 years
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Postmenopausal women between the ages of 40 and 70 years, inclusive.
  • A primary diagnosis of MDD, single or recurrent episode, without psychotic features using the modified MINI International Neuropsychiatric Interview (MINI).
  • Montgomery-Asberg Depression Rating Scale (MADRS) total score > or = 22 at the screening and baseline visit.

Who cannot join

  • Use of oral estrogen-, progestin-, androgen-, or Selective Estrogen Receptor Modulator (SERM)-containing drug products 8 weeks before baseline.
  • Current (within 12 months) psychoactive substance abuse or dependence (including alcohol), manic episode, post-traumatic stress disorder, obsessive-compulsive disorder, or a lifetime diagnosis of bipolar or psychotic disorder.
  • A history or active presence of clinically important medical disease.
  • Additional criteria apply.

Trial locations and contacts

70 sites in 6 countries.

70 sites in 6 countries

United States52 sites
  • Study site

    Atlanta, Georgia, 30328

  • Study site

    Baltimore, Maryland, 21208

  • Study site

    Bellaire, Texas, 77401

  • Study site

    Boston, Massachusetts, 02114

  • Study site

    Brooksville, Florida, 34613

  • Study site

    Burlington, Vermont, 05401

  • Study site

    Charleston, South Carolina, 29407

  • Study site

    Charlottesville, Virginia, 22903

  • Study site

    Columbia, South Carolina, 29201

  • Study site

    Coral Springs, Florida, 33065

  • Study site

    Cromwell, Connecticut, 06416

  • Study site

    Dallas, Texas, 75235

  • Study site

    Denton, Texas, 76201

  • Study site

    Denver, Colorado, 80212

  • Study site

    East Providence, Rhode Island, 02914

  • Study site

    Elmsford, New York, 10523

  • Study site

    Fall River, Massachusetts, 02721

  • Study site

    Farmington, Connecticut, 06030

  • Study site

    Fort Myers, Florida, 33912

  • Study site

    Gainesville, Florida, 32607

  • Study site

    Hollis, New York, 11423

  • Study site

    Houston, Texas, 77090

  • Study site

    Las Vegas, Nevada, 89106

  • Study site

    Lincoln, Rhode Island, 02865

  • Study site

    Maitland, Florida, 32751

  • Study site

    Memphis, Tennessee, 38117

  • Study site

    Middleton, Wisconsin, 53562

  • Study site

    Morgantown, West Virginia, 26506

  • Study site

    Mt. Pleasant, South Carolina, 29464

  • Study site

    New Orleans, Louisiana, 70115

  • Study site

    New York, New York, 10032

  • Study site

    New York, New York, 10128

  • Study site

    Northfield, Illinois, 60093

  • Study site

    Oak Brook, Illinois, 60523

  • Study site

    Oklahoma City, Oklahoma, 73103

  • Study site

    Overland Park, Kansas, 66211

  • Study site

    Pasadena, California, 91107

  • Study site

    Peoria, Arizona, 85381

  • Study site

    Philadelphia, Pennsylvania, 19104

  • Study site

    Piscataway, New Jersey, 08854

  • Study site

    Pittsburgh, Pennsylvania, 15206

  • Study site

    Pittsburgh, Pennsylvania, 15213

  • Study site

    Raleigh, North Carolina, 27612

  • Study site

    Richmond, Virginia, 23230

  • Study site

    Roswell, Georgia, 30076

  • Study site

    Saint Paul, Minnesota, 55101

  • Study site

    San Diego, California, 92103

  • Study site

    San Diego, California, 92108

  • Study site

    Shreveport, Louisiana, 71130

  • Study site

    Syracuse, New York, 13210

  • Study site

    Waterbury, Connecticut, 06708

  • Study site

    Wichita, Kansas, 67214

Other trials in United States

Argentina9 sites
  • Study site

    Buenos Aires, 1062

  • Study site

    Buenos Aires, 1119

  • Study site

    Buenos Aires, 1126

  • Study site

    Buenos Aires, 1205

  • Study site

    Buenos Aires, 1221

  • Study site

    Buenos Aires, 1414

  • Study site

    Buenos Aires, 1425

  • Study site

    La Plata, 1900

  • Study site

    Mendoza, 5500

Other trials in Argentina

Colombia3 sites
  • Study site

    Barranquilla

  • Study site

    Bogotá

  • Study site

    Bucamaranga

Other trials in Colombia

Mexico3 sites
  • Study site

    Mexico City

  • Study site

    Monterrey

  • Study site

    Tobasco

Other trials in Mexico

Peru2 sites
  • Study site

    Chiclayo

  • Study site

    Lima

Other trials in Peru

Chile1 site
  • Study site

    Santiago

Other trials in Chile

About this study

Official title: A Multicenter, Randomized, 8-Week Double-Blind Acute Phase Followed By a 6-Month Continuation Phase (Open-Label Or Double-Blind) Study to Evaluate the Efficacy, Safety, and Tolerability of DVS SR Versus Escitalopram in Postmenopausal Women With Major Depressive Disorder

Desvenlafaxine succinate (DVS) is a potent and selective serotonin and norepinephrine reuptake inhibitor (SNRI). This study will investigate the safety, efficacy, and tolerability of DVS SR versus escitalopram in women with major depressive disorder (MDD) who are postmenopausal.

Being tested
Desvenlafaxine succinate sustained-release (DVS SR), Escitalopram
Keywords
MDD, Major Depressive Disorder, Depression
Medical subject headings
Depression, Depressive Disorder, Depressive Disorder, Major

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Desvenlafaxine succinate sustained-release (DVS SR)Drug

    flexible dose of DVS 50-100 or 200 mg every day during 56 days. Extension until 6 months.

  • EscitalopramDrug

    Flexible dose of Escitalopram 10 or 20 mg every day during 56 days. Extension until 6 months.

Study groups in NCT00406640
Study groupRoleWhat they receive
AActive comparatorNot described
Receives: Drug: Desvenlafaxine succinate sustained-release (DVS SR)
BActive comparatorNot described
Receives: Drug: Escitalopram

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8

    HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Items are scored on either a 3 point (0 to 2) or a 5 point scale (0 to 4) with 0=none/absent and 4=most severe,for a maximum total score of 50. Change= 8 week adjusted mean HAM-D17 minus baseline adjusted mean HAM-D17.

    Measured: Baseline and 8 weeks

Secondary outcomes (12)
  1. Percentage of Patients Achieving Response to Treatment at Final On-therapy Evaluation (Acute Phase)

    A response is defined as ≥ 50% decrease from baseline on Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Individual items are scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 8 weeks

  2. Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase)

    Remission is defined as a Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score of ≤ 7. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Individual items are scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 8 weeks

  3. Clinical Global Impression Improvement (CGI-I) Score at 8 Weeks

    CGI-I is a global rating scale that measures disease improvement. Using a 7-point scale, the clinician rates how much the patient's illness has improved or worsened relative to the baseline status (1= very much improved; 7= very much worse).

    Measured: 8 weeks

  4. Change in Clinical Global Impression Severity (CGI-S) Score From Baseline to Week

    CGI-S is a global rating scale that measures the severity of a patient's disease. Using a 7-point scale, the clinician rates the severity of the patient's mental illness at the time of the assessment, relative to the clinician's experience with patients who have the same diagnosis (1= normal; 7= extremely ill).

    Measured: Baseline and 8 weeks

  5. Change in Hamilton Psychiatric Rating Scale for Anxiety From Baseline to Week 8 (HAM-A) Score

    The HAM-A is a standardized, clinician-administered rating scale that assesses 14 items characteristically associated with major anxiety disorders. Items are scaled 0 - 4 (0=none and 4=very severe), with a maximum total score of 56. Change= 8 week adjusted mean HAM-A total score minus baseline adjusted mean total score.

    Measured: Baseline and Week 8

  6. Change in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 8

    EQ-5D is a standardized, subject-administered measure of health outcome. It provides a descriptive profile for 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression), using 3 levels (no, moderate, or extreme problems) and a single index value characterizing current health status using a 100-point visual analog scale (0=worst, 100=best). EQ-5D summary index is obtained with a formula that weights each level of the dimensions. The index-based score is interpreted along a continuum of 0 (death) to 1 (perfect health). Change=8 week score minus baseline score.

    Measured: Baseline and week 8

  7. Percentage of Responders Maintaining Response to Treatment at Final On-therapy Evaluation (Double Blind Continuation Phase)

    Patients achieving a response to treatment at the end of the 8-week acute double blind (DB) phase continued the same treatment in a 6-month DB continuation phase and were evaluated to see if the response was maintained. A response is defined as ≥ 50% decrease from baseline on Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Individual items are scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 6 months

  8. Percentage of Responders Achieving Remission at Final On-therapy Evaluation (Double Blind Continuation Phase)

    Patients achieving a response to treatment at the end of the 8-week acute double blind (DB) phase continued the same treatment in a 6-month DB continuation phase and were evaluated to see if remission was achieved. Remission is defined as a Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score of ≤ 7. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Individual items are scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 6 months

  9. Percentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase

    Patients achieving a response to treatment (Responders) at the end of the 8-week acute double blind (DB) phase continued into a 6-month DB phase. Responders without remission at 8 weeks were assessed for remission status during the 6-month continuation. Remission defined as a Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score ≤ 7. HAM-D17 is a standardized, clinician-administered rating scale assessing 17 items characteristically associated with major depression. Individual items scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 6 months

  10. Percentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase

    Patients who didn't achieve a response to treatment at the end of the 8-week acute double blind phase entered into an OL treatment phase with DVS SR for 6 months and were evaluated to see if a response was achieved. A response is defined as ≥ 50% decrease from baseline on Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Individual items are scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 6 months

  11. Percentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase

    Patients who did not achieve a response to treatment at the end of the 8-week acute double blind phase entered into an open label (OL) treatment phase with DVS SR for 6 months and were evaluated to see if remission was achieved. Remission is defined as a Hamilton Psychiatric Rating Scale for Depression (HAM-D17) score of ≤ 7. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression. Individual items are scored on a 0 to 2 or 4 scale (0=none/absent and 4=most severe) for a maximum total score of 50.

    Measured: 6 months

  12. Discontinuation-Emergent Signs and Symptoms (DESS) Total Score

    DESS is a clinician-administered 43-item assessment that evaluates discontinuation-emergent symptoms resulting from the withdrawal from test article. The DESS total score is the sum of the number of new symptoms and old (but worse) symptoms that appeared during tapering of the test article. A higher score indicates more symptoms. The DESS score was assessed by status of taper.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Dec 2006 (estimated)
  2. Study startDec 2006
  3. Primary completionFeb 2008
  4. Study completionOct 2008

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Single group
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
595 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00406640
Sponsor's protocol ID
3151A1-402
Status last verified
Dec 2023
First submitted
29 Nov 2006
Last updated
28 Dec 2023

Publications

  • Soares CN, Thase ME, Clayton A, Guico-Pabia CJ, Focht K, Jiang Q, Kornstein SG, Ninan PT, Kane CP. Open-label treatment with desvenlafaxine in postmenopausal women with major depressive disorder not responding to acute treatment with desvenlafaxine or escitalopram. CNS Drugs. 2011 Mar;25(3):227-38. doi: 10.2165/11586460-000000000-00000.

    PubMed 21323394

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Desvenlafaxine succinate sustained-release (DVS SR) and Escitalopram in people with Depression and Depressive Disorder, run by Wyeth is now a wholly owned subsidiary of Pfizer at 70 sites in 6 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 70 sites in United States, Argentina, Colombia, Mexico, Peru and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 29 Jun 2010). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8 (time frame: Baseline and 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00406640, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Dec 2023.

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