Skip to content

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

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

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00406640
Enrollment
595
Registered
2006-12-04
Start date
2006-12-31
Completion date
2008-10-31
Last updated
2023-12-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Depressive Disorder, Depressive Disorder, Major

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.

DRUGEscitalopram

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

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 70 Years
Healthy volunteers
No

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

MeasureTime frameDescription
Change in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8Baseline and 8 weeksHAM-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

MeasureTime frameDescription
Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase)8 weeksRemission 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 Weeks8 weeksCGI-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 WeekBaseline and 8 weeksCGI-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) ScoreBaseline and Week 8The 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 8Baseline and week 8EQ-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 weeksA 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 monthsPatients 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 Phase6 monthsPatients 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 Phase6 monthsPatients 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 Phase6 monthsPatients 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 Score6 monthsDESS 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 monthsPatients 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

ArmCount
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
Total595

Withdrawals & dropouts

PeriodReasonFG000FG001
Acute PhaseAdverse Event1813
Acute PhaseFailed to Return51
Acute PhaseLack of Efficacy33
Acute PhaseLost to Follow-up74
Acute PhasePhysician Decision01
Acute PhaseProtocol deviation410
Acute PhaseProtocol Violation32
Acute PhaseWithdrawal by Subject119
DB Continuation Phase for RespondersAdverse Event1111
DB Continuation Phase for RespondersDeath10
DB Continuation Phase for RespondersFailed to Return02
DB Continuation Phase for RespondersLack of Efficacy11
DB Continuation Phase for RespondersLost to Follow-up17
DB Continuation Phase for Respondersnon-compliance75
DB Continuation Phase for RespondersPhysician Decision23
DB Continuation Phase for RespondersProtocol Violation22
DB Continuation Phase for RespondersWithdrawal by Subject86
OL Extension Phase for Non-RespondersAdverse Event66
OL Extension Phase for Non-RespondersFailed to Return10
OL Extension Phase for Non-RespondersLack of Efficacy67
OL Extension Phase for Non-RespondersLost to Follow-up23
OL Extension Phase for Non-Respondersnon-compliance32
OL Extension Phase for Non-RespondersPhysician Decision10
OL Extension Phase for Non-RespondersWithdrawal by Subject36

Baseline characteristics

CharacteristicDesvenlafaxine Succinate Sustained-release (DVS SR)EscitalopramTotal
Age, Continuous55.78 years
STANDARD_DEVIATION 6.13
56.15 years
STANDARD_DEVIATION 6.25
55.97 years
STANDARD_DEVIATION 6.19
Region of Enrollment
Argentina
43 participants42 participants85 participants
Region of Enrollment
Chile
11 participants9 participants20 participants
Region of Enrollment
Colombia
21 participants20 participants41 participants
Region of Enrollment
Mexico
10 participants9 participants19 participants
Region of Enrollment
United States
211 participants219 participants430 participants
Sex: Female, Male
Female
296 Participants299 Participants595 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
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

Primary

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.

ArmMeasureValue (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 scaleStandard Error 0.42
EscitalopramChange in Hamilton Psychiatric Rating Scale for Depression (HAM-D17) Score From Baseline to Week 8-14.30 units on scaleStandard Error 0.4
Comparison: DVS SR compared with ESCp-value: 0.24395% CI: [-0.46, 1.81]Mixed Models Analysis
Secondary

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.

ArmMeasureValue (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 scaleStandard Error 0.09
EscitalopramChange in Clinical Global Impression Severity (CGI-S) Score From Baseline to Week-2.22 units on scaleStandard Error 0.08
p-value: 0.23995% CI: [-0.09, 0.37]Mixed Models Analysis
Secondary

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.

ArmMeasureValue (MEAN)Dispersion
Desvenlafaxine Succinate Sustained-release (DVS SR)Change in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 80.25 units on scaleStandard Error 0.02
EscitalopramChange in Dimension Health State EuroQol (EQ-5D) Score From Baseline to Week 80.24 units on scaleStandard Error 0.02
Comparison: DVS SR compared to ESCp-value: 0.63595% CI: [-0.03, 0.06]Mixed Models Analysis
Secondary

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.

ArmMeasureValue (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 scaleStandard Deviation 0.42
EscitalopramChange in Hamilton Psychiatric Rating Scale for Anxiety From Baseline to Week 8 (HAM-A) Score-11.73 units on scaleStandard Deviation 0.4
Comparison: DVS SR compared to ESCp-value: 0.51695% CI: [-0.75, 1.49]Mixed Models Analysis
Secondary

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.

ArmMeasureValue (MEAN)Dispersion
Desvenlafaxine Succinate Sustained-release (DVS SR)Clinical Global Impression Improvement (CGI-I) Score at 8 Weeks1.93 units on scaleStandard Error 0.08
EscitalopramClinical Global Impression Improvement (CGI-I) Score at 8 Weeks1.81 units on scaleStandard Error 0.07
Comparison: DVS SR compared with ESCp-value: 0.2695% CI: [-0.09, 0.33]Mixed Models Analysis
Secondary

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).

ArmMeasureGroupValue (MEAN)Dispersion
Desvenlafaxine Succinate Sustained-release (DVS SR)Discontinuation-Emergent Signs and Symptoms (DESS) Total ScoreEnd of Therapy1.49 units on scaleStandard Deviation 3.09
Desvenlafaxine Succinate Sustained-release (DVS SR)Discontinuation-Emergent Signs and Symptoms (DESS) Total ScoreTaper week 11.18 units on scaleStandard Deviation 2.12
Desvenlafaxine Succinate Sustained-release (DVS SR)Discontinuation-Emergent Signs and Symptoms (DESS) Total ScoreTaper week 22.29 units on scaleStandard Deviation 3.46
Desvenlafaxine Succinate Sustained-release (DVS SR)Discontinuation-Emergent Signs and Symptoms (DESS) Total ScorePost-taper1.61 units on scaleStandard Deviation 3.55
EscitalopramDiscontinuation-Emergent Signs and Symptoms (DESS) Total ScorePost-taper1.48 units on scaleStandard Deviation 2.86
EscitalopramDiscontinuation-Emergent Signs and Symptoms (DESS) Total ScoreEnd of Therapy1.52 units on scaleStandard Deviation 3.65
EscitalopramDiscontinuation-Emergent Signs and Symptoms (DESS) Total ScoreTaper week 23.16 units on scaleStandard Deviation 4.58
EscitalopramDiscontinuation-Emergent Signs and Symptoms (DESS) Total ScoreTaper week 11.68 units on scaleStandard Deviation 3.28
Comparison: DVS SR vs. ESC: end of therapyp-value: 0.927t-test, 2 sided
Comparison: DVS SR vs. ESC: after 1 week of taperp-value: 0.055t-test, 2 sided
Comparison: DVS SR vs. ESC: after 2 weeks of taperp-value: 0.025t-test, 2 sided
Comparison: DVS SR vs. ESC: after \> 2 weeks of taperp-value: 0.653t-test, 2 sided
Secondary

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.

ArmMeasureValue (NUMBER)
Desvenlafaxine Succinate Sustained-release (DVS SR)Percentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase40.6 Percentage of Non-Responders
EscitalopramPercentage of Non-Responders Achieving Remission at Final Evaluation of 6-month Open-Label Extension Phase47.5 Percentage of Non-Responders
Secondary

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.

ArmMeasureValue (NUMBER)
Desvenlafaxine Succinate Sustained-release (DVS SR)Percentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase39.1 Percentage of Non-Responders
EscitalopramPercentage of Non-Responders Achieving Response at Final Evaluation of 6-month Open-Label (OL)Extension Phase50.8 Percentage of Non-Responders
Secondary

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.

ArmMeasureValue (NUMBER)
Desvenlafaxine Succinate Sustained-release (DVS SR)Percentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase)37.9 Percentage of patients
EscitalopramPercentage of Patients Achieving Remission at Final On-therapy Evaluation (Acute Phase)48.1 Percentage of patients
Comparison: DVS SR compared with ESC.p-value: 0.005495% CI: [0.39, 0.85]Chi-squared
Secondary

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.

ArmMeasureValue (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
EscitalopramPercentage of Patients Achieving Response to Treatment at Final On-therapy Evaluation (Acute Phase)73.4 percentage of patients
Comparison: DVS SR compared with ESC.p-value: 0.07795% CI: [0.4, 0.92]Chi-squared
Secondary

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.

ArmMeasureValue (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
EscitalopramPercentage of Responders Achieving Remission at Final On-therapy Evaluation (Double Blind Continuation Phase)61.3 percentage of responders
Comparison: DVS SR compared with ESC.p-value: 0.23495% CI: [0.83, 2.16]Chi-squared
Secondary

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.

ArmMeasureValue (NUMBER)
Desvenlafaxine Succinate Sustained-release (DVS SR)Percentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase88.9 percentage of responders
EscitalopramPercentage of Responders Improving Response to Remission During 6-month Double Blind Continuation Phase81.8 percentage of responders
Secondary

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.

ArmMeasureValue (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
EscitalopramPercentage of Responders Maintaining Response to Treatment at Final On-therapy Evaluation (Double Blind Continuation Phase)80.0 percentage of responders
Comparison: DVS SR compared with ESC.p-value: 0.70295% CI: [0.63, 2]Chi-squared

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026