Evidence map›Paper›PMID 22229314›Full record

ReviewCNS & neurological disorders drug targets2011

Monoclonal antibodies as pharmacokinetic antagonists for the treatment of (+)-methamphetamine addiction.

S Michael Owens, William T Atchley, Michael D Hambuchen, Eric C Peterson, W Brooks Gentry

Abstract readReview
In one paragraph

Review in CNS & neurological disorders drug targets, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Methamphetamine Dysregulation of the Central Nervous System and Peripheral Immunity.The Journal of pharmacology and experimental therapeutics · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Effect of Bile Duct Ligation-induced Liver Dysfunction on Methamphetamine Pharmacokinetics and Locomotor Activity in Rats.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Nanomedicine: Going small to beat the high.Nature nanotechnology · 2016
    Article
  18. Article
  19. Article
  20. Article
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

5 authors at 1 institution in 1 country.

S Michael OwensDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. mowens@uams.edu
William T Atchley
Michael D Hambuchen
Eric C Peterson
W Brooks Gentry
University of Arkansas for Medical Sciences · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR029884 · NCRR · UNIV OF ARKANSAS FOR MED SCIS · PI LOWERY, CURTIS L · 2009 to 2011
$11.4M
Arkansas Center for Clinical and Translational ResearchUL1TR000039 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI BECK, CORNELIA MARIE, JAMES, LAURA P · 2012 to 2014
$10.0M
Translational Training in AddictionT32DA022981 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI Melissa Jean Zielinski · 2009 to 2026
$6.1M
Chimeric anti-Methamphetamine Monoclonal Antibody for Treating Stimulant ToxicityRC2DA028915 · NIDA · INTERVEXION THERAPEUTICS, LLC · PI GENTRY, W BROOKS, HOLTZ, R. BARRY · 2009 to 2010
$4.0M
ANTIBODY-BASED THERAPY FOR METHAMPHETAMINE ABUSER01DA011560 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI OWENS, SAMUEL MICHAEL · 1998 to 2008
$3.6M
IMMUNOTHERAPY FOR DRUG ABUSER01DA007610 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI OWENS, SAMUEL MICHAEL · 1992 to 2009
$3.4M
First Human Studies of a Chimeric Anti-Methamphetamine Monoclonal AntibodyR01DA031944 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI GENTRY, W BROOKS · 2011 to 2014
$3.1M
Mechanism-based Changes in Anti-METH Monoclonal Antibody Therapy During PregnancyF30DA029372 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI ATCHLEY, WILLIAM THOMAS · 2011 to 2013
$92k
NCATS NIH HHS UL1 TR000039NCRR NIH HHS 1UL1RR029884NCRR NIH HHS UL1 RR029884NIDA NIH HHS DA031944NIDA NIH HHS DA07610NIDA NIH HHS DA11560NIDA NIH HHS F30 DA029372NIDA NIH HHS R01 DA007610NIDA NIH HHS R01 DA011560NIDA NIH HHS R01 DA031944NIDA NIH HHS RC2 DA028915NIDA NIH HHS RC2DA028915
6 · The paper itself

Abstract

Developing specific medications to treat (+)-methamphetamine (METH) addiction is a difficult challenge because METH has multiple sites of action that are intertwined with normal neurological function. As a result, no small molecule medication for the treatment of METH addiction has made it through the FDA clinical trials process. With the invention of a new generation of proteinbased therapies, it is now possible to consider treating drug addiction by an entirely different approach. This new approach is based on the discovery of very high affinity anti-METH monoclonal antibodies (mAbs), which are non-addictive and antagonize METH effects from the blood stream without entering the brain. Due to a very long biological half-life, anti-METH mAbs would only need to be administered once every 2-4 weeks, aiding in patient compliance. As a relapse prevention medication, anti-METH mAbs could reduce or prevent the rewarding effects of a relapse to METH use and thereby improve a patient's probability of remaining in therapy and recovering from their addiction. In this review, we discuss the discovery process of anti-METH mAbs, with a focus on the preclinical development leading to high affinity anti-METH mAb antagonists.

Indexed as

AnimalsAntibodies, MonoclonalClinical Trials as TopicHumansMethamphetamineSubstance-Related DisordersTreatment OutcomeAntibodies, MonoclonalMethamphetamine

Identifiers

PMID22229314
PMCPMC3653579
OpenAlexW2118998593

What OpenQuestion holds

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LicenceTDM
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.