Evidence map›Paper›PMID 33070154›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2021

The effects of inhibition of fatty acid amide hydrolase (FAAH) by JNJ-42165279 in social anxiety disorder: a double-blind, randomized, placebo-controlled proof-of-concept study.

Mark E Schmidt, Michael R Liebowitz, Murray B Stein, Jennifer Grunfeld, Ilse Van Hove, W Kyle Simmons, Peter Van Der Ark, James A Palmer, Ziad S Saad, Darrel J Pemberton and 2 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
8.7field-weighted citation impact, top 1% 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.

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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Endocannabinoid contributions to the perception of socially relevant, affective touch in humans.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Trial
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  5. Article
  6. Review
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  8. Research Review: What we have learned about the endocannabinoid system in developmental psychopathology.Journal of child psychology and psychiatry, and allied disciplines · 2025
    Review
  9. Review
  10. Review
  11. Fatty acid amide hydrolase in major depressive episodes: A [Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
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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

12 authors at 5 institutions in 3 countries.

Mark E SchmidtJanssen Research & Development, Beerse, Belgium. mschmid4@its.jnj.com.
Michael R LiebowitzThe Medical Research Network, New York, NY, USA.
Murray B SteinUniversity of California San Diego, La Jolla, CA, USA.
Jennifer GrunfeldPeninsula Therapeutic & Research Group, Frankston, VIC, Australia.
Ilse Van HoveJanssen Research & Development, Beerse, Belgium.
W Kyle SimmonsJanssen Research & Development, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-0399-9003
Peter Van Der ArkJanssen Research & Development, Beerse, Belgium.
James A PalmerJanssen Research & Development, La Jolla, CA, USA.
Ziad S SaadJanssen Research & Development, La Jolla, CA, USA.
Darrel J PembertonJanssen Research & Development, Beerse, Belgium.
Luc Van NuetenJanssen Research & Development, Beerse, Belgium.
Wayne C DrevetsJanssen Research & Development, La Jolla, CA, USA.
Janssen (Belgium) · BEJanssen (United States) · USMedical Research Network · USPeninsula Health · AUUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

JNJ-42165279 is a selective inhibitor of fatty acid amide hydrolase (FAAH), the enzyme responsible for the degradation of fatty acid amides (FAA) including anandamide (AEA), palmitoylethanolamide (PEA), and N-oleoylethanolamide (OEA). We assessed the efficacy, safety, tolerability, pharmacokinetics, and pharmacodynamics of treatment with JNJ-42165279 in subjects with social anxiety disorder (SAD). This was a multicenter, double-blind, placebo-controlled study randomizing subjects to 12 weeks of treatment with either JNJ-42165279 (25 mg daily) or placebo (PBO). The primary endpoint was the change in the Liebowitz Social Anxiety Scale (LSAS) total score from baseline to end of study. Secondary endpoints included the Hamilton Anxiety Scale (HAM-A), Hamilton Depression Rating Scale (HDRS

Indexed as

Phobia, SocialAmidohydrolasesDose-Response Relationship, DrugDouble-Blind MethodFatty Acid Amide HydrolasesHumansPiperazinesTreatment OutcomeAmidohydrolasesFatty Acid Amide HydrolasesJNJ-42165279Piperazines

Identifiers

PMID33070154
PMCPMC8115178
OpenAlexW3093249185

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.