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.
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
- Conditions the study is for
- Depression, Depressive Disorder, Depressive Disorder, Major
- 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
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Burlington, Vermont, 05401
Study site
Charleston, South Carolina, 29407
Study site
Charlottesville, Virginia, 22903
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Columbia, South Carolina, 29201
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Coral Springs, Florida, 33065
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Cromwell, Connecticut, 06416
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Dallas, Texas, 75235
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Denton, Texas, 76201
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Denver, Colorado, 80212
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East Providence, Rhode Island, 02914
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Elmsford, New York, 10523
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Fall River, Massachusetts, 02721
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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
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Oklahoma City, Oklahoma, 73103
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Overland Park, Kansas, 66211
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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
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
Colombia3 sites
Study site
Barranquilla
Study site
Bogotá
Study site
Bucamaranga
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.
- Conditions
- Depression, Depressive Disorder, Depressive Disorder, Major
- 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 group | Role | What they receive |
|---|---|---|
| A | Active comparator | Not described Receives: Drug: Desvenlafaxine succinate sustained-release (DVS SR) |
| B | Active comparator | Not described Receives: Drug: Escitalopram |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
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
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
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
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
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
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
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
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
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
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
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
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.
- First posted4 Dec 2006 (estimated)
- Study startDec 2006
- Primary completionFeb 2008
- Study completionOct 2008
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for DepressionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer
- Sponsor type
- Industry (pharma, biotech, devices)
- Investigators
- Medical Monitor, Study director, Wyeth is now a wholly owned subsidiary of PfizerTrial Manager, Principal investigator, For Argentina: Scheima@wyeth.comTrial Manager, Principal investigator, For Chile: scheima@wyeth.comTrial Manager, Principal investigator, For Mexico: gomezzlj@wyeth.com
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
- Results posted
- Yes, on ClinicalTrials.gov
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
Study at a glance
From the registry record, last updated by the sponsor on 28 Dec 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT00406640
- Acronym / sponsor ID
- 3151A1-402
- Conditions
- Depression, Depressive Disorder, Depressive Disorder, Major
- Keywords
- MDD, Major Depressive Disorder, Depression
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 595 participants (actual)
- Lead sponsor
- Wyeth is now a wholly owned subsidiary of PfizerIndustry (pharma, biotech, devices)
- Study start
- Dec 2006
- Primary completion
- Feb 2008 (actual)
- Study completion
- Oct 2008 (actual)
- First posted
- 4 Dec 2006 (estimated)
- Results
- Posted 29 Jun 2010
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| A | Active comparator | Drug: Desvenlafaxine succinate sustained-release (DVS SR) |
| B | Active comparator | Drug: Escitalopram |
Who may qualify
- Ages
- 40 to 70 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (4 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Desvenlafaxine succinate sustained-release (DVS SR)flexible dose of DVS 50-100 or 200 mg every day during 56 days. Extension until 6 months. | Drug | A |
| EscitalopramFlexible dose of Escitalopram 10 or 20 mg every day during 56 days. Extension until 6 months. | Drug | B |
Primary outcome
Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8
Time frame: Baseline and 8 weeks
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.
12 secondary outcomes
Percentage of Patients Achieving Response to Treatment at Final On-therapy Evaluation (Acute Phase)
Time frame: 8 weeks
Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase)
Time frame: 8 weeks
Clinical Global Impression Improvement (CGI-I) Score at 8 Weeks
Time frame: 8 weeks
Change in Clinical Global Impression Severity (CGI-S) Score From Baseline to Week
Time frame: Baseline and 8 weeks
Change in Hamilton Psychiatric Rating Scale for Anxiety From Baseline to Week 8 (HAM-A) Score
Time frame: Baseline and Week 8
Change in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 8
Time frame: Baseline and week 8
Percentage of Responders Maintaining Response to Treatment at Final On-therapy Evaluation (Double Blind Continuation Phase)
Time frame: 6 months
Percentage of Responders Achieving Remission at Final On-therapy Evaluation (Double Blind Continuation Phase)
Time frame: 6 months
Percentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase
Time frame: 6 months
Percentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase
Time frame: 6 months
Percentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase
Time frame: 6 months
Discontinuation-Emergent Signs and Symptoms (DESS) Total Score
Time frame: 6 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Dec 2023.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 21323394Soares 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Medical Monitor study director
Wyeth is now a wholly owned subsidiary of Pfizer
Trial Manager principal investigator
For Argentina: Scheima@wyeth.com
Trial Manager principal investigator
For Chile: scheima@wyeth.com
70 sites in 6 countries: see every site and its status.
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.