Evidence map›Paper›PMID 42873389›Full record

ReviewAdvances in therapy2026

Ibogaine for Substance Use Disorders.

Ahmed I Anwar, Abdul-Rahman A Hegazi, M Farris Sawaya, Joshua R Nelson, Audrey E Lashley, Jillian M Gatti, Kristy M Pham, Ibraheem A Hachem, Molly E McNulty, Destiny S Lewis and 2 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

12 authors.

Ahmed I AnwarSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA. aia003@lsuhs.edu.ORCID http://orcid.org/0000-0002-3140-357X
Abdul-Rahman A HegaziDepartment of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA, USA.
M Farris SawayaDepartment of Pharmacology, Toxicology and Neuroscience, School of Graduate Studies, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Joshua R NelsonSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Audrey E LashleySchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Jillian M GattiDepartment of Pharmacology, Toxicology and Neuroscience, School of Graduate Studies, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Kristy M PhamSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Ibraheem A HachemSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Molly E McNultyDepartment of Pharmacology, Toxicology and Neuroscience, School of Graduate Studies, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Destiny S LewisSchool of Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Kevin S MurnaneDepartment of Pharmacology, Toxicology and Neuroscience, School of Graduate Studies, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Alan D KayeDepartment of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Substance use disorders (SUDs) are a major global health burden, and psychedelic-assisted therapies are now gaining scientific interest, with ibogaine being considered as a candidate for anti-addictive effects across multiple substance classes. Ibogaine is a multi-target indole alkaloid acting on opioid, glutamatergic, serotonergic, and sigma systems with potential to rapidly reduce withdrawal and cravings after a single administration. Ibogaine is metabolized into noribogaine, which has a longer half-life and contributes to sustained pharmacological effects. These compounds act on multiple neurotransmitter systems including NMDA receptors, serotonin receptors, and opioid receptors, which allow it to have a broad neurobiological effect. It also has anti-addictive properties linked to neuroplasticity, dopamine modulation, and opioid receptor activity. Additionally, iboga has use in African rituals, with modern interest increasing in the twentieth century. Ibogaine now is an unregulated or semi-regulated substance with increased interest in controlled clinical development as well. Clinical evidence for ibogaine comes from observational studies and case reports, e.g., particularly in opioid use disorder. Ibogaine carries significant risks, particularly cardiotoxicity, neurological adverse effects including hallucinations, and reported fatalities. Safer derivates such as noribogaine and tabernanthalog (TBG) are being developed to retain anti-addictive efficacy and reduce toxicity. Ibogaine induces prolonged oneirogenic states involved in autobiographical memory processing, and outcomes are influenced by setting, integration therapy, and psychotherapy. Current research is largely observational, and studies are small, which highlights the need for standardized protocols and clinical trials. Overall, ibogaine represents a therapeutic candidate for SUDs, with broad anti-addictive potential. In this review, we provide an overview of ibogaine's history and pharmacology, critically examine its therapeutic potential in multiple SUDs, and discuss current limitations, emerging alternatives, and future directions.

Indexed as

AddictionMental illnessMethamphetamineOpioidSubstance useTreatment-seeking

Identifiers

What OpenQuestion holds

Textmetadata
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.