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  1. Article ; Online: Antagonist Treatment for Opioid Use Disorder.

    Silverman, Bernard L / Akerman, Sarah C

    The American journal of medicine

    2017  Volume 130, Issue 3, Page(s) e117

    Language English
    Publishing date 2017-03
    Publishing country United States
    Document type Letter
    ZDB-ID 80015-6
    ISSN 1555-7162 ; 1873-2178 ; 0002-9343 ; 1548-2766
    ISSN (online) 1555-7162 ; 1873-2178
    ISSN 0002-9343 ; 1548-2766
    DOI 10.1016/j.amjmed.2016.08.048
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  2. Article ; Online: Reply to Kunoe (2020) and Ghosh & Singh (2020) regarding Nunes et al. (2020): Opioid use and dropout from extended-release naltrexone in a controlled trial: implications for mechanism.

    Nunes, Edward V / Bisaga, Adam / Krupitsky, Evgeny / Nangia, Narinder / Silverman, Bernard L / Akerman, Sarah C / Sullivan, Maria A

    Addiction (Abingdon, England)

    2020  Volume 115, Issue 11, Page(s) 2188–2190

    MeSH term(s) Humans ; Naltrexone/therapeutic use ; Narcotic Antagonists/therapeutic use ; Opioid-Related Disorders/drug therapy
    Chemical Substances Narcotic Antagonists ; Naltrexone (5S6W795CQM)
    Language English
    Publishing date 2020-07-16
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 1141051-6
    ISSN 1360-0443 ; 0965-2140
    ISSN (online) 1360-0443
    ISSN 0965-2140
    DOI 10.1111/add.15153
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  3. Article ; Online: Efficacy and Safety of a Combination of Olanzapine and Samidorphan in Adult Patients With an Acute Exacerbation of Schizophrenia: Outcomes From the Randomized, Phase 3 ENLIGHTEN-1 Study.

    Potkin, Steven G / Kunovac, Jelena / Silverman, Bernard L / Simmons, Adam / Jiang, Ying / DiPetrillo, Lauren / McDonnell, David

    The Journal of clinical psychiatry

    2020  Volume 81, Issue 2

    Abstract: Objective: To assess the antipsychotic efficacy and safety of a combination of olanzapine and samidorphan (OLZ/SAM).: Methods: This 4-week, phase 3, randomized, double-blind, placebo- and olanzapine-controlled study was conducted from December 2015 ... ...

    Abstract Objective: To assess the antipsychotic efficacy and safety of a combination of olanzapine and samidorphan (OLZ/SAM).
    Methods: This 4-week, phase 3, randomized, double-blind, placebo- and olanzapine-controlled study was conducted from December 2015 to June 2017 in adults with schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria who were experiencing an acute exacerbation. Patients were randomized 1:1:1 to OLZ/SAM, olanzapine monotherapy, or placebo. The primary and key secondary efficacy endpoint assessed was the change in Positive and Negative Syndrome Scale (PANSS) total score and Clinical Global Impressions-Severity of Illness Scale (CGI-S) score between baseline and week 4, respectively, for OLZ/SAM versus placebo. Safety monitoring occurred throughout.
    Results: 401 patients received ≥ 1 dose of study drug; 352 completed treatment. Treatment with OLZ/SAM resulted in significant improvements versus placebo in PANSS total and CGI-S scores from baseline to week 4 (least squares [LS] mean ± SE: -6.4 ± 1.8 [P < .001] and -0.38 ± 0.12 [P = .002], respectively). Olanzapine treatment resulted in similar improvements (PANSS and CGI-S LS mean ± SE of -5.3 ± 1.84 [P = .004] and -0.44 ± 0.12 [P < .001], respectively). Adverse events (AEs) occurred in 54.5%, 54.9%, and 44.8% of patients on OLZ/SAM, olanzapine, and placebo, respectively. Weight gain, somnolence, dry mouth, anxiety, and headache were the most common AEs (ie, ≥ 5%) with active treatment.
    Conclusions: OLZ/SAM treatment resulted in statistically and clinically significant efficacy improvements over 4 weeks versus placebo in adults with acutely exacerbated schizophrenia. Improvements were similar to those observed with olanzapine. OLZ/SAM was well tolerated, with a safety profile similar to that of olanzapine.
    Trial registrations: ClinicalTrials.gov identifier: NCT02634346; EudraCT number: 2015-003373-15​​.
    MeSH term(s) Acute Disease ; Adult ; Antipsychotic Agents/administration & dosage ; Antipsychotic Agents/pharmacology ; Double-Blind Method ; Drug Combinations ; Female ; Humans ; Male ; Middle Aged ; Naltrexone/administration & dosage ; Naltrexone/analogs & derivatives ; Naltrexone/pharmacology ; Narcotic Antagonists/administration & dosage ; Narcotic Antagonists/pharmacology ; Olanzapine/administration & dosage ; Olanzapine/pharmacology ; Outcome Assessment, Health Care ; Schizophrenia/drug therapy ; Symptom Flare Up
    Chemical Substances Antipsychotic Agents ; Drug Combinations ; Narcotic Antagonists ; Naltrexone (5S6W795CQM) ; 3-carboxamido-4-hydroxynaltrexone (7W2581Z5L8) ; Olanzapine (N7U69T4SZR)
    Language English
    Publishing date 2020-03-03
    Publishing country United States
    Document type Clinical Trial, Phase III ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 716287-x
    ISSN 1555-2101 ; 0160-6689
    ISSN (online) 1555-2101
    ISSN 0160-6689
    DOI 10.4088/JCP.19m12769
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  4. Article ; Online: IgA deficiency destabilizes homeostasis toward intestinal microbes and increases systemic immune dysregulation.

    Conrey, Peyton E / Denu, Lidiya / O'Boyle, Kaitlin C / Rozich, Isaiah / Green, Jamal / Maslanka, Jeffrey / Lubin, Jean-Bernard / Duranova, Tereza / Haltzman, Brittany L / Gianchetti, Lauren / Oldridge, Derek A / De Luna, Nina / Vella, Laura A / Allman, David / Spergel, Jonathan M / Tanes, Ceylan / Bittinger, Kyle / Henrickson, Sarah E / Silverman, Michael A

    Science immunology

    2023  Volume 8, Issue 83, Page(s) eade2335

    Abstract: The ability of most patients with selective immunoglobulin A (IgA) deficiency (SIgAD) to remain apparently healthy has been a persistent clinical conundrum. Compensatory mechanisms, including IgM, have been proposed, yet it remains unclear how secretory ... ...

    Abstract The ability of most patients with selective immunoglobulin A (IgA) deficiency (SIgAD) to remain apparently healthy has been a persistent clinical conundrum. Compensatory mechanisms, including IgM, have been proposed, yet it remains unclear how secretory IgA and IgM work together in the mucosal system and, on a larger scale, whether the systemic and mucosal anti-commensal responses are redundant or have unique features. To address this gap in knowledge, we developed an integrated host-commensal approach combining microbial flow cytometry and metagenomic sequencing (mFLOW-Seq) to comprehensively define which microbes induce mucosal and systemic antibodies. We coupled this approach with high-dimensional immune profiling to study a cohort of pediatric patients with SIgAD and household control siblings. We found that mucosal and systemic antibody networks cooperate to maintain homeostasis by targeting a common subset of commensal microbes. In IgA-deficiency, we find increased translocation of specific bacterial taxa associated with elevated levels of systemic IgG targeting fecal microbiota. Associated features of immune system dysregulation in IgA-deficient mice and humans included elevated levels of inflammatory cytokines, enhanced follicular CD4 T helper cell frequency and activation, and an altered CD8 T cell activation state. Although SIgAD is clinically defined by the absence of serum IgA, the symptomatology and immune dysregulation were concentrated in the SIgAD participants who were also fecal IgA deficient. These findings reveal that mucosal IgA deficiency leads to aberrant systemic exposures and immune responses to commensal microbes, which increase the likelihood of humoral and cellular immune dysregulation and symptomatic disease in patients with IgA deficiency.
    MeSH term(s) Humans ; Child ; Mice ; Animals ; IgA Deficiency ; Immunoglobulin A, Secretory ; Immunoglobulin M ; Homeostasis
    Chemical Substances Immunoglobulin A, Secretory ; Immunoglobulin M
    Language English
    Publishing date 2023-05-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ISSN 2470-9468
    ISSN (online) 2470-9468
    DOI 10.1126/sciimmunol.ade2335
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  5. Article ; Online: Transition of Patients with Opioid Use Disorder from Buprenorphine to Extended-Release Naltrexone: A Randomized Clinical Trial Assessing Two Transition Regimens.

    Comer, Sandra D / Mannelli, Paolo / Alam, Danesh / Douaihy, Antoine / Nangia, Narinder / Akerman, Sarah C / Zavod, Abigail / Silverman, Bernard L / Sullivan, Maria A

    The American journal on addictions

    2020  Volume 29, Issue 4, Page(s) 313–322

    Abstract: Background and objective: When patients seek to discontinue buprenorphine (BUP) treatment, monthly injectable extended-release naltrexone (XR-NTX) may help them avoid relapse. The efficacy of low ascending doses of oral NTX vs placebo for patients ... ...

    Abstract Background and objective: When patients seek to discontinue buprenorphine (BUP) treatment, monthly injectable extended-release naltrexone (XR-NTX) may help them avoid relapse. The efficacy of low ascending doses of oral NTX vs placebo for patients transitioning from BUP to XR-NTX is evaluated in this study.
    Methods: In a phase 3, hybrid residential/outpatient study, clinically stable participants with opioid use disorder (N = 101), receiving BUP for more than or equal to 3 months and seeking antagonist treatment, were randomized (1:1) to 7 residential days of descending doses of BUP and low ascending doses of oral NTX (NTX/BUP, n = 50) or placebo (PBO-N/BUP, n = 51). Both groups received standing ancillary medications and psychoeducational counseling. Following negative naloxone challenge, participants received XR-NTX (day 8). The primary endpoint was the proportion of participants who received and tolerated XR-NTX.
    Results: There was no statistical difference between groups for participants receiving a first dose of XR-NTX: 68.6% (NTX/BUP) vs 76.0% (PBO-N/BUP; P = .407). The mean number of days with peak Clinical Opiate Withdrawal Scale (COWS) score less than or equal to 12 during the treatment period (days 1-7) was similar for NTX/BUP and PBO-N/BUP groups (5.8 vs 6.3; P = .511). Opioid withdrawal symptoms during XR-NTX induction and post-XR-NTX observation period (days 8-11) were mild and similar between groups (mean peak COWS score: NTX/BUP, 5.1 vs PBO-N/BUP, 5.4; P = .464). Adverse events were mostly mild/moderate.
    Conclusions and scientific significance: Low ascending doses of oral NTX did not increase induction rates onto XR-NTX compared with placebo. The overall rate of successful induction across treatment groups supports a brief BUP taper with standing ancillary medications as a well-tolerated approach for patients seeking transition from BUP to XR-NTX. (Am J Addict 2020;00:00-00).
    MeSH term(s) Adult ; Buprenorphine/administration & dosage ; Buprenorphine/adverse effects ; Delayed-Action Preparations ; Dose-Response Relationship, Drug ; Drug Monitoring/methods ; Drug Substitution/adverse effects ; Drug Substitution/methods ; Female ; Humans ; Male ; Naltrexone/administration & dosage ; Naltrexone/adverse effects ; Narcotic Antagonists/administration & dosage ; Narcotic Antagonists/adverse effects ; Opioid-Related Disorders/drug therapy ; Substance Withdrawal Syndrome/etiology ; Substance Withdrawal Syndrome/therapy ; Treatment Outcome
    Chemical Substances Delayed-Action Preparations ; Narcotic Antagonists ; Buprenorphine (40D3SCR4GZ) ; Naltrexone (5S6W795CQM)
    Language English
    Publishing date 2020-04-04
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial
    ZDB-ID 1141440-6
    ISSN 1521-0391 ; 1055-0496
    ISSN (online) 1521-0391
    ISSN 1055-0496
    DOI 10.1111/ajad.13024
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  6. Article ; Online: Insulin and glucose metabolism with olanzapine and a combination of olanzapine and samidorphan: exploratory phase 1 results in healthy volunteers.

    Toledo, Frederico G S / Martin, William F / Morrow, Linda / Beysen, Carine / Bajorunas, Daiva / Jiang, Ying / Silverman, Bernard L / McDonnell, David / Namchuk, Mark N / Newcomer, John W / Graham, Christine

    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

    2021  Volume 47, Issue 3, Page(s) 696–703

    Abstract: A combination of olanzapine and samidorphan (OLZ/SAM) received US Food and Drug Administration approval in May 2021 for the treatment of adults with schizophrenia or bipolar I disorder. OLZ/SAM provides the efficacy of olanzapine, while mitigating ... ...

    Abstract A combination of olanzapine and samidorphan (OLZ/SAM) received US Food and Drug Administration approval in May 2021 for the treatment of adults with schizophrenia or bipolar I disorder. OLZ/SAM provides the efficacy of olanzapine, while mitigating olanzapine-associated weight gain. This exploratory study characterized the metabolic profile of OLZ/SAM in healthy volunteers to gain mechanistic insights. Volunteers received once-daily oral 10 mg/10 mg OLZ/SAM, 10 mg olanzapine, or placebo for 21 days. Assessments included insulin sensitivity during an oral glucose tolerance test (OGTT), hyperinsulinemic-euglycemic clamp, other measures of glucose/lipid metabolism, and adverse event (AE) monitoring. Treatment effects were estimated with analysis of covariance. In total, 60 subjects were randomized (double-blind; placebo, n = 12; olanzapine, n = 24; OLZ/SAM, n = 24). Olanzapine resulted in hyperinsulinemia and reduced insulin sensitivity during an OGTT at day 19, changes not observed with OLZ/SAM or placebo. Insulin sensitivity, measured by hyperinsulinemic-euglycemic clamp, was decreased in all treatment groups relative to baseline, but this effect was greatest with olanzapine and OLZ/SAM. Although postprandial (OGTT) glucose and fasting cholesterol concentrations were similarly increased with olanzapine or OLZ/SAM, other early metabolic effects were distinct, including post-OGTT C-peptide concentrations and aspects of energy metabolism. Forty-nine subjects (81.7%) experienced at least 1 AE, most mild or moderate in severity. OLZ/SAM appeared to mitigate some of olanzapine's unfavorable postprandial metabolic effects (e.g., hyperinsulinemia, elevated C-peptide) in this exploratory study. These findings supplement the body of evidence from completed or ongoing OLZ/SAM clinical trials supporting its role in the treatment of schizophrenia and bipolar I disorder.
    MeSH term(s) Adult ; Antipsychotic Agents/pharmacology ; Glucose ; Healthy Volunteers ; Humans ; Insulin ; Naltrexone/analogs & derivatives ; Narcotic Antagonists/pharmacology ; Olanzapine/adverse effects ; United States
    Chemical Substances Antipsychotic Agents ; Insulin ; Narcotic Antagonists ; Naltrexone (5S6W795CQM) ; 3-carboxamido-4-hydroxynaltrexone (7W2581Z5L8) ; Glucose (IY9XDZ35W2) ; Olanzapine (N7U69T4SZR)
    Language English
    Publishing date 2021-12-09
    Publishing country England
    Document type Clinical Trial, Phase I ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 639471-1
    ISSN 1740-634X ; 0893-133X
    ISSN (online) 1740-634X
    ISSN 0893-133X
    DOI 10.1038/s41386-021-01244-7
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  7. Article ; Online: Effects of the Opioid System Modulator, Samidorphan, on Measures of Alcohol Consumption and Patient-Reported Outcomes in Adults with Alcohol Dependence.

    O'Malley, Stephanie S / Todtenkopf, Mark S / Du, Yangchun / Ehrich, Elliot / Silverman, Bernard L

    Alcoholism, clinical and experimental research

    2018  Volume 42, Issue 10, Page(s) 2011–2021

    Abstract: Background: Demonstrating clinically meaningful benefits of alcohol use disorder treatments is challenging.: Methods: We report findings from a 12-week, phase 2, randomized, double-blind, placebo-controlled study of samidorphan (1, 2.5, or 10 mg/d) ... ...

    Abstract Background: Demonstrating clinically meaningful benefits of alcohol use disorder treatments is challenging.
    Methods: We report findings from a 12-week, phase 2, randomized, double-blind, placebo-controlled study of samidorphan (1, 2.5, or 10 mg/d) in adults with alcohol use disorder (NCT00981617). The primary end point was percentage of subjects with no heavy drinking days (PSNHDD) during weeks 5 to 12; secondary end points included alcohol consumption measures, craving, and patient-rated outcomes.
    Results: Altogether, 406 patients were included in the full analysis set (101, 104, 100, and 101 in the placebo, samidorphan 1, 2.5, and 10 mg treatment groups, respectively). There was no statistical difference between samidorphan and placebo groups on PSNHDD during weeks 5 to 12. However, dose-dependent reductions in cumulative rate of heavy drinking days were observed (-41%, p < 0.001 for samidorphan 10 mg/d vs. placebo; -30 and -32% for samidorphan 2.5 and 1 mg, p < 0.05 for both). A higher percentage of samidorphan- than placebo-treated patients had a ≥2-category downshift in World Health Organization (WHO) risk levels of drinking. There were significant reductions from baseline with samidorphan versus placebo in alcohol craving (for samidorphan 10 mg: -38.2 [standard error: 2.9] vs. placebo: -30.2 [2.8]; p = 0.044). On a Patient Global Assessment of Response to Therapy (PGART), samidorphan 10 mg was superior to placebo at 4, 8, and 12 weeks (p < 0.001, p < 0.001, p < 0.01, respectively). Improvement in PGART correlated with a reduction in craving and a decrease in WHO risk level.
    Conclusions: Results for the primary outcome measure PSNHDD were negative, but at variance with other measures and patient treatment perceptions that may be relevant for interventional studies. These findings highlight the importance of understanding the most relevant outcomes to patients and incorporating and prioritizing patient-centered outcomes when assessing interventions for alcohol use disorder.
    MeSH term(s) Adult ; Alcohol Drinking/drug therapy ; Alcohol Drinking/psychology ; Alcohol Drinking/trends ; Alcoholism/drug therapy ; Alcoholism/psychology ; Double-Blind Method ; Female ; Humans ; Male ; Middle Aged ; Naltrexone/analogs & derivatives ; Naltrexone/pharmacology ; Naltrexone/therapeutic use ; Narcotic Antagonists/pharmacology ; Narcotic Antagonists/therapeutic use ; Patient Reported Outcome Measures ; Receptors, Opioid, mu/antagonists & inhibitors ; Treatment Outcome
    Chemical Substances Narcotic Antagonists ; Receptors, Opioid, mu ; Naltrexone (5S6W795CQM) ; 3-carboxamido-4-hydroxynaltrexone (7W2581Z5L8)
    Language English
    Publishing date 2018-08-13
    Publishing country England
    Document type Clinical Trial, Phase II ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 428999-7
    ISSN 1530-0277 ; 0145-6008
    ISSN (online) 1530-0277
    ISSN 0145-6008
    DOI 10.1111/acer.13849
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  8. Article ; Online: Multiple Systems Estimation for Sparse Capture Data: Inferential Challenges When There Are Nonoverlapping Lists

    Chan, Lax / Silverman, Bernard W. / Vincent, Kyle

    Journal of the American Statistical Association. 2021 July 3, v. 116, no. 535 p.1297-1306

    2021  

    Abstract: Multiple systems estimation strategies have recently been applied to quantify hard-to-reach populations, particularly when estimating the number of victims of human trafficking and modern slavery. In such contexts, it is not uncommon to see sparse or ... ...

    Abstract Multiple systems estimation strategies have recently been applied to quantify hard-to-reach populations, particularly when estimating the number of victims of human trafficking and modern slavery. In such contexts, it is not uncommon to see sparse or even no overlap between some of the lists on which the estimates are based. These create difficulties in model fitting and selection, and we develop inference procedures to address these challenges. The approach is based on Poisson log-linear regression modeling. Issues investigated in detail include taking proper account of data sparsity in the estimation procedure, as well as the existence and identifiability of maximum likelihood estimates. A stepwise method for choosing the most suitable parameters is developed, together with a bootstrap approach to finding confidence intervals for the total population size. We apply the strategy to two empirical datasets of trafficking in US regions, and find that the approach results in stable, reasonable estimates. An accompanying R software implementation has been made publicly available. Supplementary materials for this article are available online.
    Keywords computer software ; data collection ; humans ; population size ; statistical analysis ; Human trafficking; Log-linear models; Mark-recapture; Model identifiability; Model selection; Modern slavery
    Language English
    Dates of publication 2021-0703
    Size p. 1297-1306.
    Publishing place Taylor & Francis
    Document type Article ; Online
    ZDB-ID 2064981-2
    ISSN 1537-274X
    ISSN 1537-274X
    DOI 10.1080/01621459.2019.1708748
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  9. Article ; Online: A phase 3, multicenter study to assess the 1-year safety and tolerability of a combination of olanzapine and samidorphan in patients with schizophrenia: Results from the ENLIGHTEN-2 long-term extension.

    Kahn, René S / Silverman, Bernard L / DiPetrillo, Lauren / Graham, Christine / Jiang, Ying / Yin, Jiani / Simmons, Adam / Bhupathi, Vasudev / Yu, Bei / Yagoda, Sergey / Hopkinson, Craig / McDonnell, David

    Schizophrenia research

    2021  Volume 232, Page(s) 45–53

    Abstract: Aim: A combination of olanzapine and samidorphan (OLZ/SAM) is in development for the treatment of patients with schizophrenia or bipolar I disorder and is intended to provide the efficacy of olanzapine while mitigating olanzapine-associated weight gain. ...

    Abstract Aim: A combination of olanzapine and samidorphan (OLZ/SAM) is in development for the treatment of patients with schizophrenia or bipolar I disorder and is intended to provide the efficacy of olanzapine while mitigating olanzapine-associated weight gain. This 52-week open-label extension (NCT02873208; ENLIGHTEN-2-EXT) assessed the long-term safety and tolerability of OLZ/SAM in patients with schizophrenia.
    Methods: Patients completing the 24-week randomized, double-blind, phase 3 ENLIGHTEN-2 study (NCT02694328) comparing weight change from baseline to week 24 with OLZ/SAM versus olanzapine were eligible to enroll in the 52-week ENLIGHTEN-2-EXT study. Assessments included adverse events (AEs; each visit), weight/waist circumference (every other week for the first 8 weeks, then every 4 weeks thereafter), metabolic laboratory parameters (weeks 4, 12, 24, 36, and 52), Positive and Negative Syndrome Scale (PANSS) scores (weeks 2, 4, 8, 12, 24, 36, and 52), and Clinical Global Impression-Severity (CGI-S) scores (weeks 2 and 4, then every 4 weeks thereafter through week 48, and at week 52). Analyses were based on observed results using descriptive statistics. Baseline was relative to the first OLZ/SAM dose in the extension study.
    Results: In total, 265 patients were enrolled and received at least 1 dose of OLZ/SAM; 167 (63.0%) completed the 52-week extension study. Common AEs (≥5%) were weight decreased (n = 23; 8.7%), extra dose administered (n = 21; 7.9%), headache (n = 18; 6.8%), and weight increased (n = 16; 6.0%). At week 52, the mean (SD) change from baseline for weight and waist circumference was -0.03 (6.17) kg and - 0.35 (6.12) cm, respectively. Changes in fasting lipid and glycemic parameters were generally small and remained stable over 52 weeks. During the extension, PANSS total scores remained stable, and at week 52, 81.3% of patients had CGI-S scores of 3 or less, reflecting mild illness severity.
    Conclusions: OLZ/SAM was generally well tolerated over 52 weeks. Weight, waist circumference, metabolic laboratory parameters, and schizophrenia symptoms remained stable throughout the study.
    MeSH term(s) Antipsychotic Agents/adverse effects ; Benzodiazepines/adverse effects ; Double-Blind Method ; Humans ; Naltrexone/analogs & derivatives ; Narcotic Antagonists ; Olanzapine/adverse effects ; Schizophrenia/drug therapy ; Treatment Outcome
    Chemical Substances Antipsychotic Agents ; Narcotic Antagonists ; Benzodiazepines (12794-10-4) ; Naltrexone (5S6W795CQM) ; 3-carboxamido-4-hydroxynaltrexone (7W2581Z5L8) ; Olanzapine (N7U69T4SZR)
    Language English
    Publishing date 2021-05-17
    Publishing country Netherlands
    Document type Clinical Trial, Phase III ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 639422-x
    ISSN 1573-2509 ; 0920-9964
    ISSN (online) 1573-2509
    ISSN 0920-9964
    DOI 10.1016/j.schres.2021.04.009
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  10. Article ; Online: Mitigation of Olanzapine-Induced Weight Gain With Samidorphan, an Opioid Antagonist: A Randomized Double-Blind Phase 2 Study in Patients With Schizophrenia.

    Martin, William F / Correll, Christoph U / Weiden, Peter J / Jiang, Ying / Pathak, Sanjeev / DiPetrillo, Lauren / Silverman, Bernard L / Ehrich, Elliot W

    The American journal of psychiatry

    2019  Volume 176, Issue 6, Page(s) 457–467

    Abstract: Objective: Preclinical evidence and data from a proof-of-concept study in healthy volunteers suggest that samidorphan, an opioid antagonist, mitigates weight gain associated with olanzapine. This study prospectively compared combination therapy of ... ...

    Abstract Objective: Preclinical evidence and data from a proof-of-concept study in healthy volunteers suggest that samidorphan, an opioid antagonist, mitigates weight gain associated with olanzapine. This study prospectively compared combination therapy of olanzapine plus either samidorphan or placebo for the treatment of schizophrenia.
    Methods: This was an international, multicenter, randomized phase 2 study of olanzapine plus samidorphan in patients with schizophrenia. The study had a 1-week open-label olanzapine lead-in period followed by a 12-week double-blind treatment phase in which patients were randomly assigned in a 1:1:1:1 ratio to receive olanzapine plus placebo (N=75) or olanzapine plus 5 mg (N=80), 10 mg (N=86), or 20 mg (N=68) of samidorphan. The primary aims were to confirm that the antipsychotic efficacy of olanzapine plus samidorphan was comparable to olanzapine plus placebo, to assess the effect of combining olanzapine with samidorphan on olanzapine-induced weight gain, and to assess the overall safety and tolerability of olanzapine plus samidorphan.
    Results: Antipsychotic efficacy, as assessed by total score on the Positive and Negative Syndrome Scale (PANSS), was equivalent across all treatment groups. Treatment with olanzapine plus samidorphan resulted in a statistically significant lower weight gain (37% lower weight gain compared with olanzapine plus placebo). The least square mean percent change from baseline in body weight was 4.1% (2.9 kg) for the olanzapine plus placebo group and 2.6% (1.9 kg) for the olanzapine plus samidorphan group (2.8% [2.1 kg] for the 5 mg group, 2.1% [1.5 kg] for the 10 mg group, and 2.9% [2.2 kg] for the 20 mg group). Adverse events reported at a frequency ≥5% in any of the olanzapine plus samidorphan groups and occurring at a rate ≥2 times greater than in the olanzapine plus placebo group were somnolence, sedation, dizziness, and constipation. Other safety measures were comparable between the olanzapine plus samidorphan groups and the olanzapine plus placebo group.
    Conclusions: The antipsychotic efficacy of olanzapine plus samidorphan was equivalent to that of olanzapine plus placebo, and olanzapine plus samidorphan was associated with clinically meaningful and statistically significant mitigation of weight gain compared with olanzapine plus placebo. Olanzapine plus samidorphan was generally well tolerated, with a safety profile similar to olanzapine plus placebo.
    MeSH term(s) Adult ; Antipsychotic Agents/therapeutic use ; Constipation/chemically induced ; Dizziness/chemically induced ; Double-Blind Method ; Drug Therapy, Combination ; Female ; Humans ; Least-Squares Analysis ; Male ; Middle Aged ; Naltrexone/analogs & derivatives ; Naltrexone/therapeutic use ; Narcotic Antagonists/therapeutic use ; Olanzapine/therapeutic use ; Schizophrenia/drug therapy ; Sleepiness ; Weight Gain
    Chemical Substances Antipsychotic Agents ; Narcotic Antagonists ; Naltrexone (5S6W795CQM) ; 3-carboxamido-4-hydroxynaltrexone (7W2581Z5L8) ; Olanzapine (N7U69T4SZR)
    Language English
    Publishing date 2019-03-08
    Publishing country United States
    Document type Clinical Trial, Phase II ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 280045-7
    ISSN 1535-7228 ; 0002-953X
    ISSN (online) 1535-7228
    ISSN 0002-953X
    DOI 10.1176/appi.ajp.2018.18030280
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