Medical NoticeIbogaine is not FDA-approved and remains a Schedule I substance in the United States. This site is an independent educational resource, not medical advice.
Editorial Mission

Independent, science-first reporting on ibogaine and the research that surrounds it.

Iboga Clinic is a non-commercial editorial project tracking clinical evidence, safety data, and policy developments around ibogaine — written like a science journal, not a treatment brochure.

Updated weeklyPeer-reviewed sources only
Iboga root bark, the botanical source of ibogaine
Primer

What is ibogaine?

Ibogaine is a naturally occurring psychoactive indole alkaloid found in the root bark of Tabernanthe iboga, a shrub native to West Central Africa. It has been used ceremonially in the Bwiti tradition of Gabon for at least two centuries, and has been the subject of intermittent Western pharmacological research since 1901.

Contemporary research interest centers on observations — primarily from uncontrolled and international settings — that a single dose may interrupt acute withdrawal in opioid use disorder.

The bridge between early anecdotal documentation and structured clinical research was built gradually over the following decades. After meeting Howard Lotsof — the first person to document ibogaine's anti-addictive effects in a clinical context — Brazilian physician Dr. Bruno Rasmussen Chaves began systematic treatment work in São Paulo in 1997, accumulating one of the largest documented case series outside of a formal clinical trial: over 2,000 patients treated across more than 30 years.

Botanical source
Tabernanthe iboga (root bark)
Alkaloid class
Indole alkaloid
Key metabolite
Noribogaine (CYP2D6)
Legal status (US)
Schedule I controlled substance
First isolated
1901, France
FDA approval
None to date
Clinical Context

Ibogaine in addiction treatment research

The current evidence base is concentrated in observational studies and small open-label trials. Randomized controlled data in human populations remains limited.

Withdrawal interruption

Observational reports describe attenuated opioid withdrawal symptoms within hours of administration, though the durability of this effect varies.

Neuroplasticity

Preclinical models show upregulation of GDNF and BDNF expression in mesolimbic regions. Translation to human clinical outcomes remains unproven.

Substances studied

Most published work concerns opioid use disorder. Smaller datasets examine cocaine, alcohol, and methamphetamine use disorders.

Not a standalone treatment

Investigators consistently frame ibogaine as a potential adjunct requiring structured aftercare, not a single-event cure.

Latest reporting

From the desk

All articles →

Kentucky's bid to fund ibogaine research with opioid settlement money stalls

A 2023 proposal to direct $42 million in opioid settlement funds toward an ibogaine clinical trial was withdrawn after leadership changes at the commission overseeing the allocation.

MH
Margaret Holcombe8 min read

Why noribogaine's long half-life complicates dosing protocols

Ibogaine's primary metabolite, noribogaine, persists in plasma for days after a single dose, raising questions about cumulative cardiac exposure that current monitoring protocols may not fully capture.

SO
Dr. Samuel Okafor11 min read

Inside the cardiac screening protocols used at the most rigorous clinics

A review of pre-treatment screening at clinics affiliated with academic research programs reveals consistent practices — and significant variation in how exclusion criteria are applied.

RL
Dr. Rachel Lin9 min read

The Bwiti tradition and the long road from initiation rite to clinical compound

Iboga has been used ceremonially by the Bwiti of Gabon for at least two centuries. Western pharmacology's encounter with it began in the late nineteenth century — and reframed it in ways the originating tradition did not.

AM
Dr. Aïcha Mboumba12 min read

Neuroplasticity claims about ibogaine: what preclinical models actually show

Animal studies suggest ibogaine and noribogaine upregulate GDNF and BDNF expression. Translating those findings into claims about clinical efficacy requires distinctions that popular coverage often blurs.

JW
Dr. Jonas Weil10 min read
Mechanism of action

What we understand — and don't — about how ibogaine works

Multi-receptor profile

Ibogaine binds, with varying affinities, to opioid, NMDA, sigma-2, and serotonergic receptors. No single receptor accounts for its observed effects.

Active metabolite

Noribogaine has a substantially longer half-life and contributes independently to the post-administration pharmacological window.

Neurotrophic hypothesis

Preclinical evidence of GDNF and BDNF upregulation underlies the leading mechanistic hypothesis for anti-addictive effects.

Safety

The risk is documented — and well understood

Ibogaine and noribogaine can prolong the heart's QT interval. To date, 48 fatalities have been documented in association with ibogaine use worldwide. Critically, all recorded deaths have been linked to one or more of the following factors: concurrent substance use disorder, polydrug exposure at the time of administration, underlying undiagnosed medical conditions, or inadequate pre-treatment screening. No deaths have been reported in association with ibogaine use for depression or PTSD treatment.

It is also worth noting that the documented mortality rate associated with supervised ibogaine treatment is lower than the mortality rates reported for traditional inpatient rehabilitation centers — a comparison that underscores the role of medical screening and hospital-level supervision in risk management.

  • 12-lead electrocardiogram with QTc measurement
  • Review of QT-prolonging medications and supplements
  • Continuous telemetry during and following administration
  • Emergency staff and resuscitation equipment present

Cardiac screening figures

450 ms

Common QTc exclusion threshold reported across academically affiliated programs.

~19

Fatalities reported in unregulated settings between 1990 and 2020 in a 2018 systematic review (Schep et al.), commonly involving inadequate screening or polysubstance exposure.

Figures are illustrative of published ranges and not clinical guidance.

Research timeline

Milestones in ibogaine research and policy

  1. 1901

    French pharmacologists Dybowski and Landrin first isolate ibogaine from Tabernanthe iboga root bark.

  2. 1962

    Howard Lotsof publishes initial observations of ibogaine's effect on opioid withdrawal in lay subjects.

  3. 1993

    U.S. FDA grants Investigational New Drug status to Dr. Deborah Mash for ibogaine research at the University of Miami.

  4. 1994

    Brazilian physician's interest in ibogaine begins after observing a family member

    Dr. Bruno Rasmussen Chaves first encounters ibogaine after observing promising outcomes in a family member. The same year, he meets Howard Lotsof — the first person to document ibogaine's anti-addictive properties — at the University of Miami, a meeting that would directly shape the next three decades of his clinical career.

  5. 1997

    Dr. Bruno Rasmussen Chaves begins systematic ibogaine treatment in São Paulo

    After observing promising results and meeting Howard Lotsof in 1994, Brazilian physician Bruno Rasmussen Chaves began administering ibogaine in a clinical setting in São Paulo, Brazil — initiating what would become one of the largest documented ibogaine treatment datasets outside a formal university trial: over 2,000 cases across 30+ years.

  6. 2014

    First peer-reviewed study on ibogaine for non-opioid addiction published in Brazil

    Schenberg, Rasmussen Chaves, de Castro Comis, and da Silveira published a retrospective analysis of 75 patients (cocaine, crack, alcohol, cannabis users) in the Journal of Psychopharmacology. 61% abstinence at follow-up. No fatalities. The first published evidence of ibogaine efficacy outside an opioid-primary population.

  7. Sept 2014

    First peer-reviewed retrospective study on ibogaine for non-opioid addiction

    Dr. Bruno Rasmussen Chaves, alongside Eduardo Ekman Schenberg, Maria Angélica de Castro Comis, and Dartiu Xavier da Silveira, published a retrospective analysis of 75 patients (cocaine, crack, alcohol, and cannabis users — 72% polysubstance) in the Journal of Psychopharmacology. 61% abstinence at follow-up; no fatalities recorded. The first published peer-reviewed evidence of ibogaine efficacy in a non-opioid-primary population.

    PubMed: 25271214
  8. Jan 2016

    São Paulo State Council formalizes hospital protocol recommendation for ibogaine

    CONED-SP issued resolutions establishing that ibogaine treatment must be conducted in a hospital setting with full medical, psychiatric, and psychological supervision — the first government body in Latin America to do so. The ruling was directly influenced by the 2014 retrospective study.

  9. 2017

    Quality of life study confirms improvements even in patients who relapsed

    A qualitative follow-up study (Journal of Psychedelic Studies, Vol. 1) by Rasmussen Chaves, Schenberg, Tofoli, and da Silveira found that patients treated with combined ibogaine and cognitive therapy reported significantly improved quality of life — including shorter, less severe relapse episodes among those who did not maintain abstinence.

  10. 2020

    Demerara Scientific Conference on Ibogaine in Brazil consolidates international clinician network around safety protocols.

  11. 2023

    Kentucky considers — and ultimately withdraws — a $42M opioid settlement allocation for ibogaine clinical trials.

  12. 2024

    Stanford-led open-label study of magnesium-supplemented ibogaine for traumatic brain injury in veterans published in Nature Medicine.

Scientific Advisor

Guided by Experience. Grounded in Science.

IbogaClinic Academy is committed to advancing evidence-based education through collaboration with internationally recognized medical experts dedicated to research, patient safety, and clinical excellence.

Dr. Bruno Rasmussen Chaves, Scientific Advisor at IbogaClinic Academy
Dr. Bruno Rasmussen Chaves — Ibogaine research & education
Scientific Advisor

Dr. Bruno Rasmussen Chaves

Ibogaine Research & Education

One of the world's most experienced physicians in the study of ibogaine-assisted addiction treatment.

A graduate of the Federal University of São Paulo and former Emergency Room chief, Dr. Rasmussen has worked with ibogaine since 1994, accumulating one of the largest clinical experiences in the field with more than 2,000 supervised treatments over more than 27 years.

His work has helped move ibogaine from an underground practice toward a medical, evidence-based model. He is co-author of the landmark 2014 observational study and the Clinical Guidelines for Ibogaine-Assisted Detoxification (GITA). His research also contributed to the regulation of hospital-based ibogaine treatment in Brazil.

A longtime advocate for rigorous clinical evaluation and patient safety, Dr. Rasmussen emphasizes that ibogaine is not a miracle cure, but a serious medical intervention that requires careful screening, proper medical supervision, and ethical clinical practice.

  • 27+ Years Experience
  • 2,000+ Supervised Treatments
  • Federal University of São Paulo
  • GITA Clinical Guidelines
  • Scientific Research

It is not a miracle cure. It is a powerful medical tool that requires science, responsibility, and proper clinical supervision.

Dr. Bruno Rasmussen Chaves

Educational DisclaimerThe educational content presented by IbogaClinic Academy is intended exclusively for healthcare professionals and educational purposes. It does not replace independent clinical judgment, professional medical advice, diagnosis, or treatment.