Iboga
PLANT
Tabernanthe iboga, Central African origins, Gabonese context, conservation, stewardship.
OPEN LANE →A public reference for the plant, the molecules, the evidence, the risks, the law, and the cultures that have carried Iboga for generations. Sources labeled by type and confidence. No dosing, no referrals, no miracle claims.
Try QT prolongation · Texas SB 2308 · Noribogaine FDA · Bwiti stewardship · Hamilton Morris
Find anything fast: search a topic, then follow the source labels into evidence, safety, policy, culture, media, or trackers.
I'm a researcher · clinician · journalist · policymaker · cultural reader · general reader
Last full review · 2026-05-18346 sources indexed4 claim checks2 corrections logged
Start here
Every route starts with plain answers, then moves into sources, evidence, safety, policy, culture, or claims.
Start with what is known, what is not known, what is risky, and what is culturally protected.
Clinician Safety and evidence briefOpen the cardiac-risk frame, interaction categories, adverse-event themes, and evidence-by-condition table.
Claims Check treatment claimsReview cure language, clinic success rates, FDA-approval claims, and natural-means-safe statements.
Culture Read culture and stewardshipUse public cultural context, conservation, reciprocity, terminology, and benefit-sharing notes.
Policy Track law and policyStart with federal status, then state rows, public funding, trials, and international policy records.
Sources Open the source catalogSearch the catalog, inspect counts by source type, and export CSV or BibTeX for review.
Core terms
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.
PLANT
Tabernanthe iboga, Central African origins, Gabonese context, conservation, stewardship.
OPEN LANE →ALKALOID
The psychoactive indole alkaloid studied for substance use and TBI, with serious safety and legal constraints.
OPEN LANE →METABOLITE / DEVELOPMENT
A metabolite and current development focus. FDA permitted a phase I U.S. study in April 2026 — not approval.
OPEN LANE →18-MC, TABERNANTHALOG, ...
Biotech derivatives tracked by molecule, evidence type, sponsor, and clinical status. Not interchangeable.
OPEN LANE →Safety desk
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.
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
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
Rows are source-linked and dated so news, policy, and research signals do not blur into clinical proof.
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.
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.
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.
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.
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.
Claim checks
Cure language, FDA-approval claims, clinic success rates, and “natural means safe” claims need source checks before they are repeated.
Evidence suggests possible effects on withdrawal, craving, and relapse for some people, but cure language outruns the evidence and hides risk.
FDA allowed an early phase study to proceed. That is not approval and does not establish safety or effectiveness.
Iboga and Ibogaine can be natural and still carry serious cardiac and interaction risks.
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.