Preliminary Efficacy and Safety of Ibogaine in the Treatment of Methadone Detoxification

NCT04003948 | Completed Phase 2

• 1 other identifier: IBO-METAD-001
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

Methadone is a very long-acting opiate very difficult to detox from. In Spain there are a lot of methadone dependent people in the aftermath of the heroin epidemic of the 1980s. Many have been dependent for more than 15 years and a number of them have a relatively stable life condition (have work, family, housing, etc.) and a relatively good health condition in comparison with current heroin users. This Phase-II RCT is a collaboration with the Sant Joan Hospital in Reus, Spain. Twenty patients on the methadone maintenance program will be recruited. Patients will be randomized to two groups: One receiving 6 doses of 100 mg of ibogaine; and the other one receiving ascending doses of ibogaine (100-200-300-400-500-600). Methadone use will be interrupted and for both groups ibogaine will be administered when clinical symptoms of opioid withdrawal appear. After an ibogaine dose, when symptoms of opioid withdrawal appear again, half of the methadone dose used last time will be administered. By doing so, methadone doses will be progressively reduced until no withdrawal symptoms appear.

Conditions

Drug Dependence; Drug Use Disorders; Opioid Dependence

Keywords

Ibogaine; Methadone; Drug dependence; Addiction

Outcome Measures

Primary Outcomes (1)

• Methadone dose

  Rate of decrease of methadone dose used

  0-6 months

Secondary Outcomes (2)

• Adverse events

  0-24 hours

• Cardiovascular effects

  0-24 hours

Study Arms (2)

Fixed dose

EXPERIMENTAL

Ibogaine Hydrochloride 100 mg on each administration.

Drug: Ibogaine Hydrochloride

Ascending dose

EXPERIMENTAL

Ibogaine Hydrochloride on ascending doses (100-200-300-400-500-600).

Drug: Ibogaine Hydrochloride

Interventions

Ibogaine Hydrochloride DRUG

Fixed or ascending doses of ibogaine will be administered for the treatment of opioid withdrawal syndrome.

Ascending dose; Fixed dose

Eligibility Criteria

• Age: 18 Years - 60 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Aged between 18 and 60 years.
• Body weight within normal range (Quetelet's index between 19 and 27) expressed as weight (kg) / height (m2).
• Normal clinical records and physical examination.
• Subjects without organic disorders.
• Laboratory tests (hematology, biochemistry and urinalysis) within the range of normal values, according to the laboratory reference values of the "Hospital Universitari Sant Joan de Reus". Variations may be admitted according to the clinical criteria of the Principal Investigator.
• Clinically acceptable temperature, blood pressure and pulse rate in supine and standing position (SBP between 100-140 mm Hg/ DBP between 50-90 mm Hg / HR between 50-100 bpm). Blood pressure and pulse will be measured after a minimum of 3 minutes of resting.
• Having not participated in another clinical trial in the last 2 months.
• Free acceptance to participate in the study by obtains signed informed consent form approved by the ethics committee.
• ECG values within the range of normal values (PR \< 240 ms, QRS \< 110 ms and QTc \< 430 ms in men and QTc \< 450 ms in women, and heart rate \>50 bpm.

You may not qualify if:

• Background of allergy, idiosyncrasy or hypersensitivity to drugs..
• Intake of any medication within 2 weeks prior taking the study treatment (except for use of paracetamol in short-term symptomatic treatments), including over-the-counter products (including natural food supplements, vitamins and medicinal plants products), or any enzymatic inductor or inhibitor before the drug administration.
• Viral activity for hepatitis B, C or HIV.
• Background or clinical evidence of cardiovascular, respiratory, renal, hepatic, endocrine, gastrointestinal, hematological or neurological disease or other chronic diseases.
• History of severe psychiatric disease like psychosis, bipolar disorder or dissociative disorders, or a high risk to develop them as reported by psychometric questionnaires.
• Past or current risk of suicide.
• Having undergone major surgery during the previous 6 months before the enrollment.
• Positive results of the drugs at screening period or the day before starting treatment period: Amphetamines, Cocaine, Ethanol, Opiates (not methadone), and not prescribed Benzodiazepines (positive results may be repeated at the discretion of the PI).
• Not understanding the nature of the study and potential consequences.
• lead ECG obtained at screening with PR ≥ 220 msec, QRS ≥120 msec and QTc ≥ 440 msec for men and ≥450 for women, bradycardia (\<50 bpm) or clinically significant minor ST wave changes or any other abnormal changes on the screening ECG that would interfere with measurement of the QT interval.
• Pregnancy or lactation status (females).
• Not understanding the informed consent.

Sponsors & Collaborators

• International Center for Ethnobotanical Education, Research, and Service: lead
• Multidisciplinary Association for Psychedelic Studies: collaborator
• University Rovira i Virgili: collaborator
• Universidad Autonoma de Madrid: collaborator
• Hospital Universitari Sant Joan de Reus: collaborator
• University of Sao Paulo: collaborator

Study Sites (1)

Hospital Universitari Sant Joan

Reus, Tarragona, 43204, Spain

Location

MeSH Terms

Conditions

Substance-Related Disorders; Opioid-Related Disorders; Behavior, Addictive

Condition Hierarchy (Ancestors)

Chemically-Induced Disorders; Mental Disorders; Narcotic-Related Disorders; Compulsive Behavior; Impulsive Behavior; Behavior

Study Officials

• José Carlos Bouso, PhD

  International Center for Ethnobotanical Education, Research, and Service

  PRINCIPAL INVESTIGATOR

• Tre Borràs, MD

  Hospital Universitari Sant Joan de Reus

  PRINCIPAL INVESTIGATOR

• Genís Ona, MSc

  International Center for Ethnobotanical Education, Research, and Service

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 27, 2019
• First Posted: July 1, 2019
• Study Start: October 28, 2020
• Primary Completion: April 26, 2024
• Study Completion: April 26, 2024
• Last Updated: January 17, 2025

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

ES (1)