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Phase 2 N=44 Randomized Double-blind Basic Science

Phase IIa Study of AV411, a Glial Activation Inhibitor, for Opioid Withdrawal

Opioid-Related Disorders

Enrolled (actual)
44
Serious AEs
0.0%
Results posted
Dec 2016
Primary outcome: Primary: Subjective Opioid Withdrawal Scale Score (SOWS) — 16; 4; 24 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
AV411 (Drug); Placebo (PCB) (Drug)
Age
Adult · 21+ yrs
Sex
All
Sponsor
New York State Psychiatric Institute
Primary completion
Apr 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Subjective Opioid Withdrawal Scale Score (SOWS)
16; 4; 24
SECONDARY
The Effects of AV411 on the Analgesic Effects of Oxycodone.
40; 42; 38

Summary

Repeated use and/or abuse of opioid medications is generally associated with a characteristic withdrawal syndrome that develops after cessation of drug administration. The present study is designed to evaluate the effectiveness of AV411 to alter opioid-induced withdrawal symptoms.

Eligibility Criteria

Inclusion Criteria

  • Adults between the ages of 21 and 45
  • Current dependence on heroin according to (Diagnostic and Statistical Manual) DSM-IV criteria
  • Non-treatment seeking

Exclusion Criteria

  • Female participants who are currently pregnant or breastfeeding. Lack of effective birth control 10 days before Study Day 1 (15 days prior to the first PET scan)
  • Self-reported use of methadone, buprenorphine, or levo-alpha-acetylmethadol (LAAM) in the past 14 days
  • Participants who have a positive history of neurological illness (including epilepsy) or those who have received anti-convulsant therapy during the past 5 years
  • Liver disease requiring medication or medical treatment, and/or aspartate or alanine aminotransferase levels greater than 3 times the upper limit of normal
  • Gastrointestinal or renal disease that would significantly impair absorption, metabolism or excretion of study drug, or require medication or medical treatment
  • Neurological or psychiatric disorders including psychosis, bipolar disorder, organic brain disease, any seizure history or other disorders that require treatment or that could make study compliance difficult
  • Positive tuberculosis (PPD) TB skin test along with a clinical history and chest X-ray indicative of active tuberculosis. (Individuals who have a positive PPD test and have a negative chest X-ray, are not symptomatic for tuberculosis, and do not require anti-tuberculosis therapy will be eligible to participate. Participants will be asked if they ever tested positive for tuberculosis. If so, they will not be given a PPD and a chest X-ray and clinical history will be used for evaluation purposes).
  • Presence or positive history of severe medical illness or any cardiovascular disease or heart abnormality, such as low hemoglobin (Hb 150/90.
  • Requirement for any of the following medications (current or within the past 4 weeks): psychotropics (including sedative/hypnotics, antidepressants, neuroleptics), anticonvulsants, antihypertensives, antiarrhythmics, or antiretroviral medications,. Participants on any current psychoactive prescription medications will be excluded.
  • Current dependence (by DSM-IV criteria) on methadone, LAAM, or buprenorphine
  • Participants for whom detoxification is not "clinically recommended" such as those with a significant history of overdose following detoxification
  • Participation in an investigational drug study within the past 3 months
  • Hypersensitivity to any of the medications used in this study
  • Participants who are positive for HIV or chronic active hepatitis
  • Metal implants or paramagnetic objects contained within the body which may interfere with the MRI scan, as determined in consultation with a neuroradiologist and according to the guidelines set forth in the following reference book commonly used by neuroradiologists: "Guide to MR procedures and metallic objects" Shellock Frank G., Lippincott Williams & Wilkins Healthcare, Philadelphia, 2001.
  • Lifetime exposure to radiation in the workplace, or participation in nuclear medicine procedures, including research protocols, in the past year
  • Positive Allen Test indicating lack of collateral blood flow to hand
  • History of Reynaud's syndrome
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00723177). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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