Evidence map›Paper›PMID 41354763›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2026

ENX-104: a selective and potent D

Krishna C Vadodaria, Jordi Serrats, William Brubaker, Brian D Kangas, Diego A Pizzagalli, Dave S Garvey, Vikram Sudarsan, Kimberly E Vanover

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Krishna C VadodariaEngrail Therapeutics, San Diego, CA, USA. krishna@engrail.com.ORCID http://orcid.org/0000-0002-3455-0209
Jordi SerratsEngrail Therapeutics, San Diego, CA, USA.
William BrubakerEngrail Therapeutics, San Diego, CA, USA.
Brian D KangasHarvard Medical School, McLean Hospital, Belmont, MA, USA.ORCID http://orcid.org/0000-0002-4597-9801
Diego A PizzagalliHarvard Medical School, McLean Hospital, Belmont, MA, USA.ORCID http://orcid.org/0000-0002-7772-1143
Dave S GarveyDSG Pharma Consulting LLC, Little Rock, AR, USA.
Vikram SudarsanEngrail Therapeutics, San Diego, CA, USA.
Kimberly E VanoverEngrail Therapeutics, San Diego, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anhedonia, characterized by a diminished reactivity to pleasurable stimuli, is a core symptom across multiple neuropsychiatric disorders, including major depressive disorder. Disruptions in dopaminergic neurotransmission and dysfunction within the mesolimbic dopaminergic circuitry are key contributors to reward processing deficits. We hypothesized that low receptor occupancy-mediated antagonism of presynaptic inhibitory D

Indexed as

DopamineDopamine AntagonistsDopamine D2 Receptor AntagonistsReceptors, Dopamine D3RewardSynaptic TransmissionAnhedoniaAnimalsDose-Response Relationship, DrugMaleNucleus AccumbensRatsRats, Sprague-DawleyReceptors, Dopamine D2DopamineDopamine AntagonistsDopamine D2 Receptor AntagonistsReceptors, Dopamine D2Receptors, Dopamine D3

Identifiers

PMID41354763
PMCPMC13125307

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.