Clinical boundary Schedule I in the U.S. Serious cardiac risk Not FDA-approved No dosing or referrals Schedule I · cardiac risk Not FDA-approved · no referrals

Start here

Choose the path that matches why you came.

Every route starts with plain answers, then moves into sources, evidence, safety, policy, culture, or claims.

Core terms

Iboga, Ibogaine, Noribogaine, and analogs are not the same thing.

Plant tradition, extracted alkaloid, metabolite, and biotech derivative are separate lanes. Evidence, law, safety, and cultural context change depending on which lane you are reading.

01

Iboga

PLANT

Tabernanthe iboga, Central African origins, Gabonese context, conservation, stewardship.

OPEN LANE →
02

Ibogaine

ALKALOID

The psychoactive indole alkaloid studied for substance use and TBI, with serious safety and legal constraints.

OPEN LANE →
03

Noribogaine

METABOLITE / DEVELOPMENT

A metabolite and current development focus. FDA permitted a phase I U.S. study in April 2026 — not approval.

OPEN LANE →
04

Analogs

18-MC, TABERNANTHALOG, ...

Biotech derivatives tracked by molecule, evidence type, sponsor, and clinical status. Not interchangeable.

OPEN LANE →

Safety desk

Cardiac and interaction risk comes first.

Benefit claims are hard to interpret without the safety frame.

Published safety literature repeatedly centers the heart. QT/QTc prolongation, bradycardia, rhythm events, electrolyte abnormalities, medication interactions, polysubstance exposure, and emergency readiness shape how Ibogaine evidence is read.

QT/QTc
QT interval, QTc correction, bradycardia, arrhythmia concern, and electrolyte context appear repeatedly in safety literature.
CYP2D6
Metabolism and medication interactions matter when reading Ibogaine, Noribogaine, and analog claims.
Electrolytes
Withdrawal physiology, dehydration, electrolytes, cardiac risk, and polysubstance use can change safety interpretation.

Emergency readiness

Reputable research and clinical discussions emphasize screening, monitoring, exclusion criteria, medication review, and the ability to respond to cardiac or medical emergencies.

Open safety desk →

Evidence by condition

Read the condition, then the quality of evidence.

The same template is used for each condition: human studies, sample sizes, design quality, outcomes, limitations, safety signals, and what is not proven.

Condition Evidence Setting What's not proven
Opioid use disorder Evidence: Moderateearly human and observational Often uncontrolled, selection-biased, and setting-dependent; approved medications remain the essential comparator. Ibogaine is not proven to cure opioid addiction.
Alcohol use disorder Evidence: Moderateinvestigational Phase I permission is safety-focused and does not establish efficacy. Noribogaine is not FDA-approved for alcohol use disorder.
Traumatic brain injury Evidence: Moderatenotable open label human signal Open-label observational data can generate hypotheses but cannot establish broad efficacy. Ibogaine is not proven as a general TBI treatment.
PTSD and trauma symptoms Evidence: Moderatesecondary outcomes and observational Controlled studies with clear PTSD endpoints and adequate follow-up remain limited. Ibogaine is not proven as a PTSD treatment.
Depression and mood symptoms Evidence: Moderatesecondary outcomes and small reports Depression-specific controlled Ibogaine evidence remains limited. Ibogaine is not proven as a depression treatment.
Parkinson's disease Evidence: Lowcase report watchlist A single case cannot establish efficacy, generalizability, or safety. Ibogaine is not proven as a Parkinson's treatment.
Withdrawal Evidence: Moderateearly human signal by context Acute symptom change is easier to observe than durable relapse prevention. Craving reduction or withdrawal relief is not the same as a cure.
Cravings Evidence: Moderateearly human signal by context Acute symptom change is easier to observe than durable relapse prevention. Craving reduction or withdrawal relief is not the same as a cure.

What's moving

Latest policy, research, media, and claim updates.

Rows are source-linked and dated so news, policy, and research signals do not blur into clinical proof.

Source type: LawConfidence: High

FDA allowed an early-phase noribogaine study to proceed in the U.S.

FDA announced that DemeRx NB may begin a closely monitored phase I noribogaine hydrochloride study for alcohol use disorder. This is not drug approval, not a finding of safety or effectiveness, and not patient access guidance.

Source
Source type: LawConfidence: High

Oklahoma HB 3834 was approved by the governor.

Oklahoma's bill page shows HB 3834, the Oklahoma Breakthrough Therapy Act for ibogaine clinical trials, approved by the governor on May 12, 2026. It does not make ibogaine FDA-approved and does not erase federal Schedule I constraints.

Source
Source type: LawConfidence: High

Texas remains the central public-funding case study.

Texas SB 2308 created a pathway for a selected consortium to conduct ibogaine drug development clinical trials and includes a subchapter that applies only if FDA approves ibogaine for a medical condition. Texas law is not proof of efficacy and does not mean treatment is available outside federal law and research controls.

Source
Source type: LawConfidence: High

Tennessee HOPE Act materials describe proposed ibogaine drug-development trials.

The Tennessee fiscal note for HB 2075 / SB 2149 describes the Helping Open Pathways to Effective Treatment Act and proposed cohort-based ibogaine drug-development trials. The fiscal note is not clinical evidence and explicitly frames key activity around FDA approval and state/federal constraints.

Source
Source type: MediaConfidence: Moderate

Podcast and interview discovery is now a standing intake lane.

The source catalog contains a growing podcast/interview directory and a dedicated Listening Library Curator role. Interview statements are not treated as facts until converted into claim records and traced to supporting sources.

Source
Read the full changes feed →

Claim checks

Common statements get a verdict.

Cure language, FDA-approval claims, clinic success rates, and “natural means safe” claims need source checks before they are repeated.

VERDICT Overstated

“Ibogaine cures addiction.”

Evidence suggests possible effects on withdrawal, craving, and relapse for some people, but cure language outruns the evidence and hides risk.

VERDICT False

“The FDA allowed Noribogaine, so it is approved.”

FDA allowed an early phase study to proceed. That is not approval and does not establish safety or effectiveness.

VERDICT False

“Natural means safe.”

Iboga and Ibogaine can be natural and still carry serious cardiac and interaction risks.

Read the claim-check archive →

Culture, stewardship, conservation

Iboga begins in Central African forest and living Bwiti traditions.

Public sources place Iboga in western equatorial Africa and describe older Central African knowledge systems before colonial and biomedical documentation. Public history, conservation, terminology, and stewardship can be discussed without treating private ceremony or lineage-held knowledge as internet content.