Clinical trial

A Randomized Controlled Clinical Trial of the Neuroimmune Modulator Ibudilast for the Treatment of Alcohol Use Disorder

Name
18-000963
Description
This study is a double-blind, placebo-controlled randomized clinical trial of IBUD (50mg BID) for the treatment of Alcohol Use Disorder (AUD). Eligible participants will undergo a 12-week medication treatment period and 5 in-person visits over 16 weeks.
Trial arms
Trial start
2018-10-01
Estimated PCD
2023-04-19
Trial end
2023-04-19
Status
Completed
Phase
Early phase I
Treatment
Ibudilast
targets neurotrophin signaling and neuroimmune function
Arms:
Ibudilast
Other names:
Pinatos, MN-166
Placebo oral capsule
matched to active drug, ibudilast
Arms:
Placebo Oral Capsule
Other names:
Sugar Pill
Size
102
Primary endpoint
Percent heavy drinking days
12 week-treatment period
Eligibility criteria
Inclusion Criteria: 1. Be between the ages of 18 and 65 2. Meet current (i.e., past 12 months) DSM-5 diagnostic criteria for alcohol use disorder moderate or severe 3. Be treatment-seeking for AUD 4. Report drinking at least 28 drinks per week if male (21 drinks per week if female) in the 28 days prior to consent Exclusion Criteria: 1. Have a current (last 12 months) DSM-5 diagnosis of substance use disorder for any psychoactive substances other than alcohol and nicotine 2. Have a lifetime DSM-5 diagnosis of schizophrenia, bipolar disorder, or any psychotic disorder 3. Have a positive urine screen for narcotics, amphetamines, or sedative hypnotics; 4. Have clinically significant alcohol withdrawal symptoms as indicated by a score ≥ 10 on the Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-R) 5. Be pregnant, nursing, or planning to become pregnant while taking part in the study; and must agree to one of the following methods of birth control (if female), unless she or partner are surgically sterile: * Oral contraceptives * Contraceptive sponge * Patch * Double barrier * Intrauterine contraceptive device * Etonogestrel implant * Medroxyprogesterone acetate contraceptive injection * Complete abstinence from sexual intercourse * Hormonal vaginal contraceptive ring 6. Have a medical condition that may interfere with safe study participation (e.g., unstable cardiac, renal, or liver disease, uncontrolled hypertension or diabetes) 7. Have AST, ALT, or GGT ≥ 3 times upper normal limit 8. Have attempted suicide in the past 3 years and/or have had serious suicidal intention or plan in the past year 9. Currently be on prescription medication that contraindicates use of IBUD, including alpha or beta agonists, theophylline, or other sympathomimetic 10. Currently be on any medications for AUD or any psychotropic medications (e.g., psychostimulants and benzodiazepines) with the exception of stable antidepressants (stable dose for ≥4 weeks) 11. Have any other circumstances that, in the opinion of the investigators, compromises participant safety.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Two-Arm, Randomized, Double-Blind, Placebo-Controlled', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 102, 'type': 'ACTUAL'}}
Updated at
2024-04-24

1 organization

1 product

1 drug

1 indication

Product
Placebo