Depression, Depressive Disorder, Depressive Disorder, Major
Conditions
Keywords
MDD, Major Depressive Disorder, Depression
Brief 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.
Interventions
flexible dose of DVS 50-100 or 200 mg every day during 56 days. Extension until 6 months.
Flexible dose of Escitalopram 10 or 20 mg every day during 56 days. Extension until 6 months.
Sponsors
Study design
Eligibility
Inclusion criteria
* 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.
Exclusion criteria
* 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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8 | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase) | 8 weeks | 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. |
| Clinical Global Impression Improvement (CGI-I) Score at 8 Weeks | 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). |
| Change in Clinical Global Impression Severity (CGI-S) Score From Baseline to Week | Baseline and 8 weeks | 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). |
| Change in Hamilton Psychiatric Rating Scale for Anxiety From Baseline to Week 8 (HAM-A) Score | Baseline and Week 8 | 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. |
| Change in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 8 | Baseline and 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. |
| Percentage of Patients Achieving Response to Treatment at Final On-therapy Evaluation (Acute Phase) | 8 weeks | 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. |
| Percentage of Responders Achieving Remission at Final On-therapy Evaluation (Double Blind Continuation Phase) | 6 months | 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. |
| Percentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase | 6 months | 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. |
| Percentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase | 6 months | 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. |
| Percentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase | 6 months | 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. |
| Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | 6 months | 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. |
| Percentage of Responders Maintaining Response to Treatment at Final On-therapy Evaluation (Double Blind Continuation Phase) | 6 months | 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. |
Countries
Argentina, Chile, Colombia, Mexico, Peru, United States
Participant flow
Recruitment details
Subjects were recruited in Argentina, Chile, Colombia, Mexico and the United States from December 2006 to January 2008.
Pre-assignment details
Subjects were screened up to 4 weeks.
Participants by arm
| Arm | Count |
|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) Acute Double Blind (DB) Phase Days 1 to 7: DVS SR 50 mg/day Days 8 to 14: 100 mg/day Days 15 to 56: At the discretion of the investigator, patients assigned 100 mg/day or 200 mg/day 6-Month Continuation Phases Double Blind Continuation Phase for Responders (HAM-D17 improved ≥50% from baseline) Days 57-238: continue taking DVS SR 100 mg/day or 200 mg/day Open-Label (OL) Extension Phase for Non-Responders (HAM-D17 improved \<50% from baseline) Days 57-63: DVS SR 100 mg/day Days 64-238: At the discretion of the investigator, patients assigned DVS SR 100 mg/day or 200mg/day Taper Phase Day 239 or at discontinuation: If patient taking DVS SR 200 mg/day, then decreased to 100 mg for 7 days, and then decreased to 50 mg/day for 7 days. Patients taking DVS SR 100 mg/day decreased to 50 mg/day for 7 days. | 296 |
| Escitalopram Acute DB Phase Days 1-14:escitalopram 10mg/day; Days 15-56:discretion of the investigator patients assigned escitalopram 10mg/day or 20mg/day 6-Month Continuation Phases DB Continuation Phase for Responders (HAM-D17 improved \> 50% from baseline) Days 57-238:continue taking escitalopram 10mg/day or 20mg/day OL Extension Phase for Non-Responders (HAM-D17 improved \<50% from baseline) Days 57-63:DVS SR 100mg/day; Days 64-238:At the discretion of the investigator, patients assigned DVS SR 100mg/day or 200mg/day Taper Phase Day 239 or at discontinuation:If patient taking DVS SR 200mg/day, decreased to 100mg/day for 7 days, and then decreased to 50mg/day for 7 days. Patients taking DVS SR 100mg/day decreased to 50mg/day for 7 days. If patients taking escitalopram 20mg/day, decreased to 10mg/day for 7 days and then decreased to matching escitalopram placebo/day for 7 days. Patients taking escitalopram 10mg/day decreased to matching escitalopram placebo/day for 7 days. | 299 |
| Total | 595 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Acute Phase | Adverse Event | 18 | 13 |
| Acute Phase | Failed to Return | 5 | 1 |
| Acute Phase | Lack of Efficacy | 3 | 3 |
| Acute Phase | Lost to Follow-up | 7 | 4 |
| Acute Phase | Physician Decision | 0 | 1 |
| Acute Phase | Protocol deviation | 4 | 10 |
| Acute Phase | Protocol Violation | 3 | 2 |
| Acute Phase | Withdrawal by Subject | 11 | 9 |
| DB Continuation Phase for Responders | Adverse Event | 11 | 11 |
| DB Continuation Phase for Responders | Death | 1 | 0 |
| DB Continuation Phase for Responders | Failed to Return | 0 | 2 |
| DB Continuation Phase for Responders | Lack of Efficacy | 1 | 1 |
| DB Continuation Phase for Responders | Lost to Follow-up | 1 | 7 |
| DB Continuation Phase for Responders | non-compliance | 7 | 5 |
| DB Continuation Phase for Responders | Physician Decision | 2 | 3 |
| DB Continuation Phase for Responders | Protocol Violation | 2 | 2 |
| DB Continuation Phase for Responders | Withdrawal by Subject | 8 | 6 |
| OL Extension Phase for Non-Responders | Adverse Event | 6 | 6 |
| OL Extension Phase for Non-Responders | Failed to Return | 1 | 0 |
| OL Extension Phase for Non-Responders | Lack of Efficacy | 6 | 7 |
| OL Extension Phase for Non-Responders | Lost to Follow-up | 2 | 3 |
| OL Extension Phase for Non-Responders | non-compliance | 3 | 2 |
| OL Extension Phase for Non-Responders | Physician Decision | 1 | 0 |
| OL Extension Phase for Non-Responders | Withdrawal by Subject | 3 | 6 |
Baseline characteristics
| Characteristic | Desvenlafaxine Succinate Sustained-release (DVS SR) | Escitalopram | Total |
|---|---|---|---|
| Age, Continuous | 55.78 years STANDARD_DEVIATION 6.13 | 56.15 years STANDARD_DEVIATION 6.25 | 55.97 years STANDARD_DEVIATION 6.19 |
| Region of Enrollment Argentina | 43 participants | 42 participants | 85 participants |
| Region of Enrollment Chile | 11 participants | 9 participants | 20 participants |
| Region of Enrollment Colombia | 21 participants | 20 participants | 41 participants |
| Region of Enrollment Mexico | 10 participants | 9 participants | 19 participants |
| Region of Enrollment United States | 211 participants | 219 participants | 430 participants |
| Sex: Female, Male Female | 296 Participants | 299 Participants | 595 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 267 / — | 262 / — |
| serious Total, serious adverse events | 5 / — | 4 / — |
Outcome results
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.
Time frame: Baseline and 8 weeks
Population: Acute Double-blind phase; all randomized patients with a baseline HAM-D17 score ≥ 18, who took at least 1 dose of study drug and had at least 1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8 | -13.63 units on scale | Standard Error 0.42 |
| Escitalopram | Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8 | -14.30 units on scale | Standard Error 0.4 |
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).
Time frame: Baseline and 8 weeks
Population: Acute double-blind phase; all randomized patients with a baseline HAM-D17 score ≥18, took at least1 dose of study drug and had at least1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Change in Clinical Global Impression Severity (CGI-S) Score From Baseline to Week | -2.09 units on scale | Standard Error 0.09 |
| Escitalopram | Change in Clinical Global Impression Severity (CGI-S) Score From Baseline to Week | -2.22 units on scale | Standard Error 0.08 |
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.
Time frame: Baseline and week 8
Population: Acute Double-blind phase; all randomized patients with a baseline HAM-D17 score ≥ 18, who took at least 1 dose of study drug and had at least 1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Change in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 8 | 0.25 units on scale | Standard Error 0.02 |
| Escitalopram | Change in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 8 | 0.24 units on scale | Standard Error 0.02 |
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.
Time frame: Baseline and Week 8
Population: Acute Double-blind phase; all randomized patients with a baseline HAM-D17 score ≥ 18, who took at least 1 dose of study drug and had at least 1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Change in Hamilton Psychiatric Rating Scale for Anxiety From Baseline to Week 8 (HAM-A) Score | -11.37 units on scale | Standard Deviation 0.42 |
| Escitalopram | Change in Hamilton Psychiatric Rating Scale for Anxiety From Baseline to Week 8 (HAM-A) Score | -11.73 units on scale | Standard Deviation 0.4 |
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).
Time frame: 8 weeks
Population: Acute double-blind phase; all randomized patients with a baseline HAM-D17 score ≥18, took at least1 dose of study drug and had at least1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Clinical Global Impression Improvement (CGI-I) Score at 8 Weeks | 1.93 units on scale | Standard Error 0.08 |
| Escitalopram | Clinical Global Impression Improvement (CGI-I) Score at 8 Weeks | 1.81 units on scale | Standard Error 0.07 |
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.
Time frame: 6 months
Population: Safety population: Randomized patients who took ≥1 dose study drug. Excluded patients lost to follow-up and discontinued with \< 4 wks therapy. Patients analyzed varied by time (DVS SR, ESC): End of Therapy (n=264, 267); Taper week 1 (n=217, 227); Taper week 2 (n=222, 223); Post-taper (n=219, 223).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | End of Therapy | 1.49 units on scale | Standard Deviation 3.09 |
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | Taper week 1 | 1.18 units on scale | Standard Deviation 2.12 |
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | Taper week 2 | 2.29 units on scale | Standard Deviation 3.46 |
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | Post-taper | 1.61 units on scale | Standard Deviation 3.55 |
| Escitalopram | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | Post-taper | 1.48 units on scale | Standard Deviation 2.86 |
| Escitalopram | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | End of Therapy | 1.52 units on scale | Standard Deviation 3.65 |
| Escitalopram | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | Taper week 2 | 3.16 units on scale | Standard Deviation 4.58 |
| Escitalopram | Discontinuation-Emergent Signs and Symptoms (DESS) Total Score | Taper week 1 | 1.68 units on scale | Standard Deviation 3.28 |
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.
Time frame: 6 months
Population: All randomized patients who took at least 1 dose of study drug, who did not achieve a response to treatment (≥50% reduction of HAM-D17 total score from baseline) at the end of the acute phase (week 8), entered into the open label extension phase and had baseline and at least 1 post-baseline HAM-D17 evaluation in the acute and open label phase.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase | 40.6 Percentage of Non-Responders |
| Escitalopram | Percentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase | 47.5 Percentage of Non-Responders |
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.
Time frame: 6 months
Population: All randomized patients who took at least 1 dose of study drug, who did not achieve a response to treatment (≥50% reduction of HAM-D17 total score from baseline) at the end of the acute phase (week 8), entered into the open label extension phase and had baseline and at least 1 post-baseline HAM-D17 evaluation in the acute and open label phase.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase | 39.1 Percentage of Non-Responders |
| Escitalopram | Percentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase | 50.8 Percentage of Non-Responders |
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.
Time frame: 8 weeks
Population: Acute double-blind phase; all randomized patients with a baseline HAM-D17 score ≥18, who took at least 1 dose of study drug and had at least 1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase) | 37.9 Percentage of patients |
| Escitalopram | Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase) | 48.1 Percentage of patients |
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.
Time frame: 8 weeks
Population: Acute double-blind phase; all randomized patients with a baseline HAM-D17 score ≥18, who took at least 1 dose of study drug and had at least 1 post-baseline HAM-D17 evaluation.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Patients Achieving Response to Treatment at Final On-therapy Evaluation (Acute Phase) | 64.3 percentage of patients |
| Escitalopram | Percentage of Patients Achieving Response to Treatment at Final On-therapy Evaluation (Acute Phase) | 73.4 percentage of patients |
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.
Time frame: 6 months
Population: All randomized patients with a baseline HAM-D17 score ≥18, who took at least 1 dose of study drug, had at least 1 post-baseline HAM-D17 evaluation, achieved a response to treatment (≥50% reduction of HAM-D17 total score from baseline) at the end of the acute phase (week 8) and continued treatment in the double blind continuation phase.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Responders Achieving Remission at Final On-therapy Evaluation (Double Blind Continuation Phase) | 67.9 percentage of responders |
| Escitalopram | Percentage of Responders Achieving Remission at Final On-therapy Evaluation (Double Blind Continuation Phase) | 61.3 percentage of responders |
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.
Time frame: 6 months
Population: All randomized patients with baseline HAM-D17 score ≥18, who took ≥1 dose study drug, had ≥1 post-baseline HAM-D17 evaluation, achieved a response to treatment (≥50% reduction of HAM-D17 total score from baseline) but not remission (HAM-D17 score ≤ 7) at the end of the acute phase and continued treatment in the 6-month DB continuation phase.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase | 88.9 percentage of responders |
| Escitalopram | Percentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase | 81.8 percentage of responders |
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.
Time frame: 6 months
Population: All randomized patients with a baseline HAM-D17 score ≥18, who took at least 1 dose of study drug, had at least 1 post-baseline HAM-D17 evaluation, achieved a response to treatment (≥50% reduction of HAM-D17 total score from baseline) at the end of the acute phase (week 8) and continued treatment in the double blind continuation phase.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Desvenlafaxine Succinate Sustained-release (DVS SR) | Percentage of Responders Maintaining Response to Treatment at Final On-therapy Evaluation (Double Blind Continuation Phase) | 81.8 percentage of responders |
| Escitalopram | Percentage of Responders Maintaining Response to Treatment at Final On-therapy Evaluation (Double Blind Continuation Phase) | 80.0 percentage of responders |