Evidence mapPaperPMID 36305696Full record

Trial reportSchizophrenia bulletin2023

Reduction in Multiple Cardiometabolic Risk Factors With Combined Olanzapine/Samidorphan Compared With Olanzapine: Post Hoc Analyses From a 24-Week Phase 3 Study.

Christoph U Correll, Evan Stein, Christine Graham, Lauren DiPetrillo, Sarah Akerman, Arielle D Stanford, Ying Jiang, Sergey Yagoda, David McDonnell, Craig Hopkinson

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Schizophrenia bulletin, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02694328 (A Phase 3 Study to Evaluate Weight Gain of ALKS 3831 Compared to Olanzapine in Adults With Schizophrenia), which is not on this map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02694328 phase3completednot on this map

A Phase 3 Study to Evaluate Weight Gain of ALKS 3831 Compared to Olanzapine in Adults With Schizophrenia

TypeinterventionalSponsorAlkermes, Inc.Ran2016 to 2018Enrolled561ConditionsSchizophreniaArmsALKS 3831, Olanzapine
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  3. Antidepressant Augmentation of Antipsychotic Treatment in Schizophrenia: A Narrative Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Christoph U CorrellDepartment of Psychiatry, Zucker Hillside Hospital, Northwell Health, Glen Oaks, NY, USA.
Evan SteinMetabolic & Atherosclerosis Research Center, Cincinnati, OH, USA.
Christine GrahamAlkermes, Inc., Waltham, MA, USA.
Lauren DiPetrilloAlkermes, Inc., Waltham, MA, USA.
Sarah AkermanAlkermes, Inc., Waltham, MA, USA.
Arielle D StanfordAlkermes, Inc., Waltham, MA, USA.
Ying JiangAlkermes, Inc., Waltham, MA, USA.
Sergey YagodaAlkermes, Inc., Waltham, MA, USA.
David McDonnellAlkermes Pharma Ireland Ltd., Dublin, Ireland.
Craig HopkinsonAlkermes, Inc., Waltham, MA, USA.
Alkermes (United States) · USAlkermes (Ireland) · IEDonald & Barbara Zucker School of Medicine at Hofstra/Northwell · USLouisville Metabolic and Atherosclerosis Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and hypothesesWeight gain and adverse cardiometabolic effects often limit the clinical utility of olanzapine. In ENLIGHTEN-2, combining olanzapine with the opioid receptor antagonist samidorphan (OLZ/SAM) mitigated olanzapine-associated weight gain. These analyses tested the hypothesis that OLZ/SAM would be associated with reduced adverse cardiometabolic effects compared with olanzapine. STUDY

designThis phase 3 double-blind study randomized adults with schizophrenia to OLZ/SAM or olanzapine for 24 weeks. Post hoc analyses assessed changes from baseline to week 24 in cardiometabolic risk parameters, including body mass index (BMI), risk of developing obesity (BMI ≥30 kg/m2) or metabolic syndrome, waist circumference, along with mean and potentially clinically significant changes in blood pressure, glucose, and lipids.

resultsAfter 24 weeks' treatment, compared with olanzapine, OLZ/SAM was associated with smaller least-squares mean (LSM) changes from baseline in systolic blood pressure (LSM difference, -2.63 mm Hg; 95% CI: -4.78, -0.47), diastolic blood pressure (LSM difference, -0.75 mm Hg; 95% CI: -2.31, 0.80), and BMI (LSM difference, -0.65 kg/m2; 95% CI: -1.01, -0.28). OLZ/SAM treatment was also associated with reduced risk of shifting from normal blood pressure to stage 1/2 hypertension (odds ratio [OR], 0.48; 95% CI: 0.24, 0.96), becoming obese (OR, 0.52; 95% CI: 0.32, 0.82), and developing metabolic syndrome (OR, 0.55; 95% CI: 0.31, 0.99) compared with olanzapine. No treatment group differences were noted for risk of hyperglycemia or hyperlipidemia.

conclusionsOLZ/SAM treatment was associated with lower risk of worsening cardiometabolic risk factors related to obesity, hypertension, and metabolic syndrome relative to olanzapine. NCT02694328, https://clinicaltrials.gov/ct2/show/NCT02694328.

Indexed as

Antipsychotic AgentsCardiovascular DiseasesHypertensionMetabolic SyndromeAdultBenzodiazepinesCardiometabolic Risk FactorsHumansNaltrexoneObesityOlanzapineWeight Gain3-carboxamido-4-hydroxynaltrexoneAntipsychotic AgentsBenzodiazepinesNaltrexoneOlanzapine3-carboxamido-4-hydroxynaltrexonedyslipidemiahyperglycemiahypertensionmetabolic syndromeschizophrenia

Identifiers

PMID36305696
PMCPMC10016392
OpenAlexW4307500299

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.