Evidence map›Paper›PMID 36905498›Full record

Trial reportAdvances in therapy2023

Patient and Healthcare Professional Preferences for Characteristics of Long-Acting Injectable Antipsychotic Agents for the Treatment of Schizophrenia.

Delbert G Robinson, Mark Suett, Amanda Wilhelm, Nayla Chaijale, Kelli R Franzenburg, Sanjay Gandhi, Blaine Cloud, Marko Mychaskiw

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Advances in therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03893825 (A Study to Evaluate the Safety, Tolerability, and Effect of Risperidone Extended-Release Injectable Suspension), which is not on this map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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.

NCT03893825 phase3completednot on this map

A Study to Evaluate the Safety, Tolerability, and Effect of Risperidone Extended-Release Injectable Suspension (TV-46000) for Subcutaneous Use as Maintenance Treatment in Adult and Adolescent Patients With Schizophrenia

TypeinterventionalSponsorTeva Branded Pharmaceutical Products R&D, Inc.Ran2019 to 2021Enrolled336ConditionsSchizophreniaArmsTV-46000, Placebo
3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

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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

8 authors.

Delbert G RobinsonDepartments of Psychiatry and Molecular Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA. drobinso@northwell.edu.ORCID 0000-0001-6606-4507
Mark SuettGlobal Medical Affairs, Teva UK Limited, Harlow, UK.
Amanda WilhelmNorth America Medical Affairs, Teva Branded Pharmaceutical Products R&D, Inc., Parsippany, NJ, USA.
Nayla ChaijaleGlobal Medical Affairs, Teva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Kelli R FranzenburgGlobal Medical Affairs, Teva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Sanjay GandhiGlobal Health Economics and Outcomes Research, Teva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Blaine CloudClinical SCORE, Chadds Ford, PA, USA.
Marko MychaskiwGlobal Health Economics and Outcomes Research, Teva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionStudies evaluating patient and healthcare professional (HCP) preferences regarding long-acting injectable (LAI) antipsychotic agent attributes are lacking.

methodsSurveys were administered to physicians, nurses, and patients who had at least two experiences with TV-46000, an investigational subcutaneous LAI antipsychotic agent for the treatment of schizophrenia, as part of the SHINE study (NCT03893825). Survey topics included preferences for route of administration, potential LAI dosing intervals (once-weekly, twice a month, once a month [q1m], every 2 months [q2m]), injection location, ease of use, syringe type, needle length, and need for reconstitution.

resultsPatients (n = 63) had a mean (SD) age of 35.6 (9.6) years, age at diagnosis of 18 (10) years, and were mostly male (75%). There were 49 HCPs: 24 physicians and 25 nurses. Patients rated "a short needle" (68%), a "choice of [q1m or q2m] dosing interval" (59%), and "injection instead of oral tablet" (59%) as the most important features. HCPs rated "single injection to initiate treatment" (61%), "flexible dosing interval" (84%), and "injection instead of oral tablet" (59%) as the most important features. Subcutaneous injections were rated "easy to [receive/administer]" by 62% of patients and 84% of HCPs. When choosing between subcutaneous injections and intramuscular injections, 65% of HCPs preferred subcutaneous injections and 57% of patients preferred intramuscular injections. It was important to most HCPs to have four dose strength options (78%), a prefilled syringe (96%), and no need for reconstitution (90%).

conclusionsPatients had a range of responses, and on some issues patient and HCP preferences differed. Altogether, this suggests the importance of providing patients with a range of options and the importance of patient-HCP discussions on treatment preference for LAIs.

Indexed as

Antipsychotic AgentsPhysiciansSchizophreniaAdultDelayed-Action PreparationsDelivery of Health CareFemaleHumansInjections, IntramuscularMaleAntipsychotic AgentsDelayed-Action PreparationsAntipsychotic agentEase of useLong-acting injectableSchizophrenia

Identifiers

PMID36905498
PMCPMC10129959

What OpenQuestion holds

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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 OpenQuestion graph.