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  1. Article ; Online: Efficacy and safety of lemborexant in midlife women with insomnia disorder.

    Terauchi, Masakazu / Cheng, Jocelyn Y / Yardley, Jane / Pinner, Kate / Moline, Margaret / Malhotra, Manoj / Inabe, Kanako / Nishida, Maika / Pappadopulos, Elizabeth

    Menopause (New York, N.Y.)

    2023  Volume 30, Issue 8, Page(s) 839–848

    Abstract: Objective: Insomnia is common in midlife women. The efficacy and safety of lemborexant (LEM), a competitive dual orexin receptor antagonist, was assessed for 12 months in a subgroup of midlife women (age, 40-58 y) from Study E2006-G000-303 (Study 303; ... ...

    Abstract Objective: Insomnia is common in midlife women. The efficacy and safety of lemborexant (LEM), a competitive dual orexin receptor antagonist, was assessed for 12 months in a subgroup of midlife women (age, 40-58 y) from Study E2006-G000-303 (Study 303; SUNRISE-2).
    Methods: This was a randomized, double-blind, placebo (PBO)-controlled (first 6 mo) study of adults with insomnia disorder ( N = 949). During treatment period 1 (TP1), participants received PBO or LEM 5 mg (LEM5) or 10 mg (LEM10). During TP2 (second 6 mo), LEM participants continued their assigned dose; PBO participants were rerandomized to LEM5 or LEM10. Assessments included patient-reported sleep- and fatigue-related measures and treatment-emergent adverse events.
    Results: The midlife female subgroup comprised 280 of 949 participants (TP1: PBO, n = 90 of 318 [28.3%]; LEM5, n = 82 of 316 [25.9%]; LEM10, n = 108 of 315 [34.3%]). At 6 months, median changes from baseline in subjective sleep-onset latency (in minutes) were -17.9, -20.7, and - 30.4 for PBO, LEM5, and LEM10 (vs PBO: LEM5, P = not significant; LEM10, P = 0.0310). At 6 months, mean changes from baseline in subjective wake after sleep onset (in minutes) were -37.0 (59.6), -50.1 (74.5), and -54.5 (65.4) for PBO, LEM5, and LEM10 (vs PBO: LEM5 and LEM10, P = not significant), with benefits sustained through 12 months. Greater decreases from baseline (improvement) in Insomnia Severity Index total score and Fatigue Severity Scale total score were seen with LEM versus PBO at 6 months; benefits continued through 12 months. Most treatment-emergent adverse events were mild to moderate in severity.
    Conclusions: Consistent with the total population, subjective sleep parameters improved, and improvement was sustained over time in midlife women. LEM was well tolerated, suggesting that LEM may be a potential treatment option for midlife women with insomnia.
    MeSH term(s) Adult ; Female ; Humans ; Middle Aged ; Double-Blind Method ; Pyridines/therapeutic use ; Pyrimidines/therapeutic use ; Sleep Initiation and Maintenance Disorders/drug therapy ; Treatment Outcome ; Menopause ; Perimenopause
    Chemical Substances lemborexant (0K5743G68X) ; Pyridines ; Pyrimidines
    Language English
    Publishing date 2023-06-20
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1205262-0
    ISSN 1530-0374 ; 1072-3714
    ISSN (online) 1530-0374
    ISSN 1072-3714
    DOI 10.1097/GME.0000000000002209
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  2. Article ; Online: Impact of lemborexant treatment on insomnia severity: analyses from a 12-month study of adults with insomnia disorder.

    Roth, Thomas / Rosenberg, Russell / Morin, Charles M / Yardley, Jane / Pinner, Kate / Perdomo, Carlos / Atkins, Norman / Pappadopulos, Elizabeth / Malhotra, Manoj / Moline, Margaret

    Sleep medicine

    2022  Volume 90, Page(s) 249–257

    Abstract: Objective/background: Evaluate changes in insomnia severity in subjects with moderate to severe insomnia (Insomnia Severity Index [ISI] score ≥15) treated for 12 months nightly with lemborexant.: Patients/methods: This phase 3 randomized study ... ...

    Abstract Objective/background: Evaluate changes in insomnia severity in subjects with moderate to severe insomnia (Insomnia Severity Index [ISI] score ≥15) treated for 12 months nightly with lemborexant.
    Patients/methods: This phase 3 randomized study comprised two 6-month treatment periods. In Period 1, 949 subjects were randomized to placebo, lemborexant 5 mg (LEM5) or 10 mg (LEM10). In Period 2, placebo subjects were rerandomized to LEM5 or LEM10; subjects initially randomized to lemborexant continued their assigned treatment. Insomnia severity was assessed using baseline ISI and 1-, 3-, 6-, 9-, and 12-month post-treatment scores.
    Results: Mean ISI scores improved significantly across treatment groups and disease severities, with greater decreases from baseline in the LEM5 and LEM10 versus placebo groups at months 1 (-7.1, -7.2, -5.2, respectively), 3 (-8.6, -8.9, -6.1, respectively), and 6 (-9.9, -9.8, -7.2 respectively); ISI score improvements were maintained with LEM5 and LEM10 at months 9 (-11.1 and -11.2, respectively) and 12 (-11.5 and -11.2, respectively). At months 1, 3, and 6, significantly more treatment responders (≥7-point ISI score decrease from baseline) were observed with LEM5 (44%-57%) and LEM10 (44%-52%) versus placebo (30%-41%). At months 1, 3, and 6, more remitters (ISI total score <10 and < 8) were observed with LEM5 (30%-44% and 22%-34%, respectively) and LEM10 (31%-41% and 22%-31%, respectively) versus placebo (18%-28% and 11%-21%, respectively).
    Conclusions: Lemborexant significantly reduced insomnia severity for 12 months and increased clinically meaningful response and remission rates versus placebo.
    Clinical trial registration: ClinicalTrials.gov, NCT02952820; ClinicalTrialsRegister.eu, EudraCT Number 2015-001463-39.
    MeSH term(s) Adult ; Double-Blind Method ; Humans ; Pyridines/therapeutic use ; Pyrimidines ; Sleep Initiation and Maintenance Disorders/drug therapy ; Treatment Outcome
    Chemical Substances Pyridines ; Pyrimidines ; lemborexant (0K5743G68X)
    Language English
    Publishing date 2022-02-08
    Publishing country Netherlands
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2012041-2
    ISSN 1878-5506 ; 1389-9457
    ISSN (online) 1878-5506
    ISSN 1389-9457
    DOI 10.1016/j.sleep.2022.01.024
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  3. Article ; Online: Economic and humanistic burden associated with noncommunicable diseases among adults with depression and anxiety in the United States.

    Armbrecht, Eric / Shah, Anuj / Schepman, Patricia / Shah, Ruchit / Pappadopulos, Elizabeth / Chambers, Richard / Stephens, Jennifer / Haider, Seema / McIntyre, Roger S

    Journal of medical economics

    2020  Volume 23, Issue 9, Page(s) 1032–1042

    Abstract: Aims: ...

    Abstract Aims:
    MeSH term(s) Absenteeism ; Adult ; Age Factors ; Anxiety Disorders/epidemiology ; Anxiety Disorders/psychology ; Chronic Disease ; Cost of Illness ; Cross-Sectional Studies ; Depressive Disorder, Major/epidemiology ; Depressive Disorder, Major/psychology ; Female ; Health Expenditures ; Health Resources ; Humans ; Male ; Middle Aged ; Noncommunicable Diseases/economics ; Noncommunicable Diseases/epidemiology ; Noncommunicable Diseases/psychology ; Quality of Life/psychology ; Retrospective Studies ; Severity of Illness Index ; Sex Factors ; Socioeconomic Factors ; United States/epidemiology
    Language English
    Publishing date 2020-06-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 2270945-9
    ISSN 1941-837X ; 1369-6998
    ISSN (online) 1941-837X
    ISSN 1369-6998
    DOI 10.1080/13696998.2020.1776297
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Clustering patients by depression symptoms to predict venlafaxine ER antidepressant efficacy: Individual patient data analysis.

    Kato, Masaki / Asami, Yuko / Wajsbrot, Dalia B / Wang, Xuemei / Boucher, Matthieu / Prieto, Rita / Pappadopulos, Elizabeth

    Journal of psychiatric research

    2020  Volume 129, Page(s) 160–167

    Abstract: Objective: To identify clusters of patients with major depressive disorder (MDD) based on the baseline 17-item Hamilton Rating Scale for Depression (HAM-D: Methods: Cluster analysis was performed to identify clusters based on standardized HAM-D: ... ...

    Abstract Objective: To identify clusters of patients with major depressive disorder (MDD) based on the baseline 17-item Hamilton Rating Scale for Depression (HAM-D
    Methods: Cluster analysis was performed to identify clusters based on standardized HAM-D
    Results: In 2599 patients, 3 patient clusters were identified, characterized as High modified Core (mCore) Symptoms/High Anxiety (cluster 1), High mCore Symptoms/Medium Anxiety (cluster 2), and Medium mCore Symptoms/Medium Anxiety (cluster 3). Significant effects of VEN vs placebo were observed on change from baseline in HAM-D
    Conclusions: Three unique clusters of patients were identified differing in baseline mCore symptoms and anxiety. Cluster membership may predict efficacy outcomes and contribute to dose effects in patients treated with VEN.
    Clinical trials registration: NCT01441440; other studies included in this analysis were conducted before the requirement to register clinical studies took effect.
    MeSH term(s) Antidepressive Agents/therapeutic use ; Cluster Analysis ; Cyclohexanols/therapeutic use ; Data Analysis ; Depression ; Depressive Disorder, Major/drug therapy ; Double-Blind Method ; Humans ; Serotonin Uptake Inhibitors/therapeutic use ; Treatment Outcome ; Venlafaxine Hydrochloride/therapeutic use
    Chemical Substances Antidepressive Agents ; Cyclohexanols ; Serotonin Uptake Inhibitors ; Venlafaxine Hydrochloride (7D7RX5A8MO)
    Language English
    Publishing date 2020-07-09
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 3148-3
    ISSN 1879-1379 ; 0022-3956
    ISSN (online) 1879-1379
    ISSN 0022-3956
    DOI 10.1016/j.jpsychires.2020.06.011
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  5. Article ; Online: Healthcare resource use and cost associated with timing of pharmacological treatment for major depressive disorder in the United States: a real-world study.

    McIntyre, Roger S / Prieto, Rita / Schepman, Patricia / Yeh, Yu-Chen / Boucher, Matthieu / Shelbaya, Ahmed / Chambers, Richard / Gao, Xin / Pappadopulos, Elizabeth

    Current medical research and opinion

    2019  Volume 35, Issue 12, Page(s) 2169–2177

    Abstract: Background: ...

    Abstract Background:
    MeSH term(s) Adult ; Antidepressive Agents/therapeutic use ; Cost-Benefit Analysis ; Depressive Disorder, Major/drug therapy ; Depressive Disorder, Major/economics ; Depressive Disorder, Major/epidemiology ; Early Medical Intervention/economics ; Early Medical Intervention/standards ; Female ; Health Care Rationing/methods ; Humans ; Male ; Serotonin Uptake Inhibitors/therapeutic use ; Serotonin and Noradrenaline Reuptake Inhibitors/therapeutic use ; Treatment Outcome ; United States/epidemiology
    Chemical Substances Antidepressive Agents ; Serotonin Uptake Inhibitors ; Serotonin and Noradrenaline Reuptake Inhibitors
    Language English
    Publishing date 2019-09-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80296-7
    ISSN 1473-4877 ; 0300-7995
    ISSN (online) 1473-4877
    ISSN 0300-7995
    DOI 10.1080/03007995.2019.1652053
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  6. Article: Economic and Humanistic Burden Associated with Depression and Anxiety Among Adults with Non-Communicable Chronic Diseases (NCCDs) in the United States.

    Armbrecht, Eric / Shah, Ruchit / Poorman, Gregory W / Luo, Linlin / Stephens, Jennifer M / Li, Benjamin / Pappadopulos, Elizabeth / Haider, Seema / McIntyre, Roger S

    Journal of multidisciplinary healthcare

    2021  Volume 14, Page(s) 887–896

    Abstract: Introduction: Patients with both major depressive disorder (MDD) and generalized anxiety disorder (GAD) in addition to one or multiple comorbid non-communicable chronic diseases (NCCDs) face unique challenges. However, few studies have characterized how ...

    Abstract Introduction: Patients with both major depressive disorder (MDD) and generalized anxiety disorder (GAD) in addition to one or multiple comorbid non-communicable chronic diseases (NCCDs) face unique challenges. However, few studies have characterized how the burden of co-occurring MDD and GAD differs from that of only MDD or only GAD among patients with NCCDs.
    Methods: In this study, we used Medical Expenditures Panel Survey data from 2010-2017 to understand how the economic and humanistic burden of co-occurring MDD and GAD differs from that of MDD or GAD alone among patients with NCCDs. We used generalized linear models to investigate this relationship and controlled for patient sociodemographics and clinical characteristics.
    Results: Co-occurring MDD and GAD was associated with increases in mean annual per patient inpatient visits, office visits, emergency department visits, annual drug costs, and total medical costs. Among patients with 3+ NCCDs, MDD or GAD only was associated with lower odds ratios (ORs) of limitations in activities of daily living (ADLs; 0.532 and 0.508, respectively) and social (0.503, 0.526) and physical limitations (0.613, 0.613) compared to co-occurring MDD and GAD. Compared to patients with co-occurring MDD and GAD, having MDD only or GAD only was associated with significantly lower odds of cognitive limitations (0.659 and 0.461, respectively) in patients with 1-2 NCCDs and patients with 3+ NCCDs (0.511, 0.416).
    Discussion: Comorbid MDD and GAD was associated with higher economic burden, lower quality of life, and greater limitations in daily living compared to MDD or GAD alone. Health-related economic and humanistic burden increased with number of NCCDs.
    Language English
    Publishing date 2021-04-23
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2453343-9
    ISSN 1178-2390
    ISSN 1178-2390
    DOI 10.2147/JMDH.S280200
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  7. Article ; Online: Impact of sertraline daily treatment regimen on adherence, persistence and healthcare resource utilisation in patients with major depressive disorder or obsessive-compulsive disorder: A real-world evidence analysis from the United States.

    Wang, Gang / Si, Tianmei / Imperato, Joseph S / Yang, LiLi / Zou, Kelly H / Jin, Ying Olive / Pappadopulos, Elizabeth A / Yan, Lei / Li, Jim Z / Yu, Wei

    International journal of clinical practice

    2021  Volume 75, Issue 10, Page(s) e14522

    Abstract: Objective: To generate real-world evidence (RWE) from the United States to assess the impact of pill burden and the importance of achieving a stable daily dose of sertraline (time taken, number of dose adjustments needed) on adherence/persistence and ... ...

    Abstract Objective: To generate real-world evidence (RWE) from the United States to assess the impact of pill burden and the importance of achieving a stable daily dose of sertraline (time taken, number of dose adjustments needed) on adherence/persistence and healthcare resource utilisation (HCRU).
    Methods: Retrospective analysis of the PharMetrics
    Results: Of 224 412 eligible patients, 108 729 stabilised on sertraline (50, 100 or 150 mg/d) and formed Cohorts 1-5. Stabilised patients on lower pill burden had statistically higher adherence and were more likely to remain persistent throughout 1-year post-index period vs patients on higher pill burden but same overall dose (100 mg/d [Cohort 2 vs 3] and 150 mg/d [Cohort 4 vs 5], respectively). Patients who did not stabilise had significantly lower adherence/persistence vs patients who achieved stable daily dose (Cohorts 1-5 combined). Persistence improved when stable daily dose was achieved quickly (within 1-4 months) and efficiently (within 1-3 dose adjustments). Probability of HCRU increased for patients who did not stabilise on their initial prescription.
    Conclusion: Simplifying treatment regimen and decreasing pill burden improved adherence and/or persistence with sertraline therapy (100 or 150 mg/d). Patients achieving stable daily dose of sertraline in an efficient and timely manner were more likely to remain persistent throughout 1-year follow-up.
    MeSH term(s) Depressive Disorder, Major/drug therapy ; Humans ; Medication Adherence ; Obsessive-Compulsive Disorder/drug therapy ; Patient Acceptance of Health Care ; Retrospective Studies ; Sertraline ; United States
    Chemical Substances Sertraline (QUC7NX6WMB)
    Language English
    Publishing date 2021-07-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 1386246-7
    ISSN 1742-1241 ; 1368-5031
    ISSN (online) 1742-1241
    ISSN 1368-5031
    DOI 10.1111/ijcp.14522
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  8. Article ; Online: Effect of desvenlafaxine 50 mg and 100 mg on energy and lassitude in patients with major depressive disorder: A pooled analysis.

    Lam, Raymond W / Wajsbrot, Dalia B / Meier, Ellen / Pappadopulos, Elizabeth / Mackell, Joan A / Boucher, Matthieu

    Journal of psychopharmacology (Oxford, England)

    2017  Volume 31, Issue 9, Page(s) 1204–1214

    Abstract: Nine randomized, double-blind, placebo-controlled studies of major depressive disorder were pooled to evaluate the effects of desvenlafaxine 50- and 100-mg/d on energy and lassitude in adults with major depressive disorder ( n=4279). Changes from ... ...

    Abstract Nine randomized, double-blind, placebo-controlled studies of major depressive disorder were pooled to evaluate the effects of desvenlafaxine 50- and 100-mg/d on energy and lassitude in adults with major depressive disorder ( n=4279). Changes from baseline to endpoint in 17-item Hamilton Rating Scale for Depression (HAM-D
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antidepressive Agents/therapeutic use ; Depressive Disorder, Major/drug therapy ; Desvenlafaxine Succinate/therapeutic use ; Double-Blind Method ; Fatigue/drug therapy ; Female ; Humans ; Male ; Middle Aged ; Psychiatric Status Rating Scales ; Young Adult
    Chemical Substances Antidepressive Agents ; Desvenlafaxine Succinate (ZB22ENF0XR)
    Language English
    Publishing date 2017-07-18
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 639313-5
    ISSN 1461-7285 ; 0269-8811
    ISSN (online) 1461-7285
    ISSN 0269-8811
    DOI 10.1177/0269881117719261
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  9. Article ; Online: A meta-analysis of the efficacy of venlafaxine extended release 75-225 mg/day for the treatment of major depressive disorder.

    Thase, Michael / Asami, Yuko / Wajsbrot, Dalia / Dorries, Kathleen / Boucher, Matthieu / Pappadopulos, Elizabeth

    Current medical research and opinion

    2017  Volume 33, Issue 2, Page(s) 317–326

    Abstract: Objective: To evaluate the short-term efficacy of venlafaxine extended release (ER) 75-225 mg/day compared with placebo for treating major depressive disorder (MDD) and to examine associations between baseline characteristics and efficacy outcomes in ... ...

    Abstract Objective: To evaluate the short-term efficacy of venlafaxine extended release (ER) 75-225 mg/day compared with placebo for treating major depressive disorder (MDD) and to examine associations between baseline characteristics and efficacy outcomes in MDD patients treated with venlafaxine ER 75-225 mg/day.
    Research design and methods: This meta-analysis included published and unpublished short-term, double-blind, placebo-controlled, Wyeth/Pfizer sponsored studies of venlafaxine ER at doses up to 225 mg/day in adults with MDD.
    Clinical trial registration: All trials were conducted before trial registration became mandatory.
    Main outcome measures: Change from baseline in the 17-item Hamilton Rating Scale for Depression (HAM-D
    Results: The full analysis set included 1087 patients from five studies that fulfilled selection criteria. Statistically significant separation between venlafaxine ER and placebo groups for HAM-D
    Conclusions: Venlafaxine ER 75-225 mg/day effectively reduced symptoms of depression in patients with MDD overall and in patients with either lower (≤23) or higher (>23) HAM-D
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antidepressive Agents, Second-Generation/administration & dosage ; Delayed-Action Preparations ; Depressive Disorder, Major/drug therapy ; Female ; Humans ; Male ; Middle Aged ; Venlafaxine Hydrochloride/administration & dosage
    Chemical Substances Antidepressive Agents, Second-Generation ; Delayed-Action Preparations ; Venlafaxine Hydrochloride (7D7RX5A8MO)
    Language English
    Publishing date 2017-02
    Publishing country England
    Document type Journal Article ; Meta-Analysis
    ZDB-ID 80296-7
    ISSN 1473-4877 ; 0300-7995
    ISSN (online) 1473-4877
    ISSN 0300-7995
    DOI 10.1080/03007995.2016.1255185
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  10. Article ; Online: Restoring function in major depressive disorder: A systematic review.

    Sheehan, David V / Nakagome, Kazuyuki / Asami, Yuko / Pappadopulos, Elizabeth A / Boucher, Matthieu

    Journal of affective disorders

    2017  Volume 215, Page(s) 299–313

    Abstract: Background: Functional impairment contributes to significant disability and economic burden in major depressive disorder (MDD). Treatment response is measured by improvement in depressive symptoms, but functional improvement often lags behind ... ...

    Abstract Background: Functional impairment contributes to significant disability and economic burden in major depressive disorder (MDD). Treatment response is measured by improvement in depressive symptoms, but functional improvement often lags behind symptomatic improvement. Residual deficits are associated with relapse of depressive symptoms.
    Methods: A literature search was conducted using the following terms: "major depressive disorder," "functional impairment," "functional outcomes," "recovery of function," "treatment outcome," "outcome assessment," "social functioning," "presenteeism," "absenteeism," "psychiatric status rating scales," and "quality of life." Search limits included publication date (January 1, 1995 to August 31, 2016), English language, and human clinical trials. Controlled, acute-phase, nonrecurrent MDD treatment studies in adults were included if a functional outcome was measured at baseline and endpoint.
    Results: The qualitative analysis included 35 controlled studies. The Sheehan Disability Scale was the most commonly used functional assessment. Antidepressant treatments significantly improved functional outcomes. Early treatment response predicted functional improvement, while baseline disease severity did not.
    Limitations: Clinical studies utilized various methodologies and assessments for functional impairment, and were not standardized or adequately powered.
    Conclusions: The lack of synchronicity between symptomatic and functional improvement highlights an unmet need for MDD. Treatment guided by routine monitoring of symptoms and functionality may minimize residual functional impairments.
    MeSH term(s) Antidepressive Agents/therapeutic use ; Depressive Disorder, Major/psychology ; Depressive Disorder, Major/therapy ; Humans ; Psychiatric Status Rating Scales ; Psychomotor Performance ; Quality of Life ; Recovery of Function
    Chemical Substances Antidepressive Agents
    Language English
    Publishing date 2017-06
    Publishing country Netherlands
    Document type Journal Article ; Meta-Analysis ; Review
    ZDB-ID 135449-8
    ISSN 1573-2517 ; 0165-0327
    ISSN (online) 1573-2517
    ISSN 0165-0327
    DOI 10.1016/j.jad.2017.02.029
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