Evidence map›Paper›PMID 40817174›Full record

Trial reportPsychopharmacology2026

The GPR139 agonist TAK-041 produces time-dependent alterations to cerebral blood flow and reward system function in patients with schizophrenia: a randomised placebo-controlled trial.

Peter C T Hawkins, Adam J Schwarz, James M Stone, Fiona Pepper, James Gilleen, Sam Gijsen, Ndabezinhle Mazibuko, Dimitrios Arkilo, Wei Yin, Jingtao Wu and 6 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03319953 (A Randomized, Double-Blind, Placebo Controlled, Two-Period Cross-Over, Proof of Activity Study to Evaluate the Effects of TAK-041 on Motivational Anhedonia as Add-On to Antipsychotics in Subjects With Stable Schizophrenia), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT03319953 phase2completednot on this map

A Randomized, Double-Blind, Placebo Controlled, Two-Period Cross-Over, Proof of Activity Study to Evaluate the Effects of TAK-041 on Motivational Anhedonia as Add-On to Antipsychotics in Subjects With Stable Schizophrenia

TypeinterventionalSponsorNeurocrine BiosciencesRan2017 to 2019Enrolled23ConditionsStable SchizophreniaArmsTAK-041, Placebo, Second Generation Antipsychotics (SGA)
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Peter C T HawkinsCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK.
Adam J SchwarzTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
James M StoneCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK.
Fiona PepperCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK.
James GilleenCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK.
Sam GijsenCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK.
Ndabezinhle MazibukoCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK.
Dimitrios ArkiloTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Wei YinTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Jingtao WuTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Polyna KhudyakovTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Rhett BehrjeTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Laura RosenTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Joel PosenerTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA.
Mitul A MehtaCentre for Neuroimaging Sciences, Institute of Psychiatry, Psychology & Neurosciences, King's College London, London, SE5 8AF, UK. Mitul.Mehta@kcl.ac.uk.ORCID http://orcid.org/0000-0003-1152-5323
Antonio LaurenzaTakeda Pharmaceuticals Ltd, Cambridge, MA, 02139, USA. antonio.laurenza@takeda.com.

Funding

Takeda Pharmaceuticals U.S.A. Takeda Pharmaceuticals U.S.A.
6 · The paper itself

Abstract

The negative and cognitive symptoms of schizophrenia are predictive of quality of life and functional recovery, but there are no approved drug options that target these symptoms directly. TAK-041 (also known as NBI-1065846) is a selective and potent small-molecule agonist of GPR139, an orphan G-protein-coupled receptor, which has been shown to reverse deficits related to negative and cognitive symptoms in animal models. In this proof-of-activity study to evaluate the effects of TAK-041 on motivational anhedonia, 23 adults with schizophrenia experiencing moderate to severe negative symptoms were administered a single 40 mg or 160 mg dose of TAK-041 in a randomised, double-blind, placebo-controlled, two-period crossover design. Functional magnetic resonance imaging (fMRI) assessment of reward function (monetary incentive delay [MID] task) and cerebral blood flow (CBF), as well as cognitive assessment with the Brief Assessment of Cognition in Schizophrenia (BACS) tool, were performed 3 h post dose and after 14 days. There was no significant effect of TAK-041 compared with placebo on BACS score at either timepoint. There was also no significant effect of TAK-041 on MID fMRI at day 1; however, at day 14, TAK-041 produced an increase in reward anticipatory activity in the ventral striatum compared with placebo. There was a significant decrease in CBF throughout the brain at day 1 that then reversed, resulting in a relative increase at day 14, compared with placebo. At day 14 there was a significant interaction between drug and CBF on reward anticipatory BOLD, indicating that drug-related changes to CBF may partially contribute to the observed BOLD effects (although the main effect of drug on the BOLD signal remained significant after including CBF as a covariate in the model). These data indicate that TAK-041 produces detectable changes in both CBF and reward task related fMRI signal in brain regions linked with symptoms and treatment response in schizophrenia. IND Number: 130074| EudraCT Number: 2017-001084-20| Clincaltrails.gov registry: NCT03319953.

Indexed as

Cerebrovascular CirculationReceptors, G-Protein-CoupledRewardSchizophreniaAcetamidesAdultAnhedoniaCognitionCross-Over StudiesDose-Response Relationship, DrugDouble-Blind MethodFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedAcetamidesReceptors, G-Protein-CoupledTAK-041Triazines

Identifiers

PMID40817174
PMCPMC13035629

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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.