Safety Study of a Disrupted Adenovirus (Ad) Serotype Cocaine Vaccine for Cocaine-dependent Individuals
Launched by WEILL MEDICAL COLLEGE OF CORNELL UNIVERSITY · May 26, 2015
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new type of vaccine designed to help people who are dependent on cocaine. The vaccine, called dAd5GNE, aims to create a response in the body that helps block the effects of cocaine on the brain, potentially aiding in recovery from addiction. The study will include participants aged 21 to 69 who have been diagnosed with a cocaine use disorder and have used cocaine within the last 60 days. It’s important for potential participants to be in good overall health and not have severe mental health issues or significant heart problems.
If you meet the eligibility requirements, you can expect to participate in treatments while also being involved in behavioral therapy programs. This trial is currently recruiting participants, and those who join will be closely monitored for safety and how well the vaccine works. Please note that this study is specifically for individuals who are committed to making a change and are looking for help with their cocaine dependency.
Gender
ALL
Eligibility criteria
- • Accrual will be random, with no bias as to gender or racial/ethnic group. Because the accrual process will be random, it is possible that there may be differences in the proportion of males and females, and racial/ethnic groups among the study individuals. All subjects will be concurrently participating in behavioral therapy programs run by Dr. Beeder's clinical team. Each case will be reviewed with the Eligibility Committee, comprised of three investigators other than the PI, to determine eligibility. The Principal Investigator will not participate in this process.
- • All subjects must fulfill all inclusion criteria and none of the exclusion criteria in order to participate in this study.
- Inclusion Criteria:
- • 1. All subjects should be able to provide informed consent.
- • 2. Must provide HIV informed consent.
- • 3. Males and females, 21- 69 years of age.
- • 4. Individuals that have been diagnosed with a cocaine use disorder according to DSM-V-TR criteria, with documented evidence of cocaine use within the past 60 days and have previously used an average of 1 to 10 grams of powdered and/or crack cocaine (via insufflation or smoking only) per week. Any prior 1 to 4 month period of cocaine abstinence in the past year will be excluded when calculating average cocaine use to evaluate study eligibility.
- • 6. Fertile males and females must agree to use adequate forms of contraception for the duration of the entire study.
- • 7. Body weight \> 45 kg.
- Exclusion Criteria:
- • 1. Individuals not deemed in good overall health by the investigator.
- • 2. Diagnosed history of severe psychotic disorders.
- • 3. Abnormal EKG at screening with changes consistent with cardiac disease.
- • 4. History of significant cardiovascular disease, hypertension, prior myocardial infarction and/or cerebrovascular event.
- • 5. Individuals who are currently on beta-blockers.
- • 6. Physical signs or laboratory values suggestive of systemic disorders.
- • 7. History of attempted suicide, as assessed by Columbia-Suicide Severity Rating Scale (C-SSRS) and/or committed homicide.
- • 8. History of diagnosed obsessive compulsive disorder (OCD).
- • 9. Known allergy to soy.
- • 10. Individuals who are currently taking alprazolam (Xanax) or ziprasidone (Geodon).
- • 11. Evidence of active infection of any types, including COVID-19, or positive for human immunodeficiency virus (HIV).
- • 12. Historical or current use of immunomodulators or immunosuppressants \<5 years prior to screening.
- • 13. Receipt of blood within 3 months of screening.
- • 14. Females who are pregnant or nursing.
- • 15. Concurrent participation in any other FDA approved Investigational New Drug.
- • 16. Abnormal liver function (transaminases greater than 2x the upper limit of normal values)
- • 17. eGFR \<30 mL/min/1.73 m2
- 18. Severe substance use disorder based on DSM-V-TR criteria (excluding cocaine, nicotine, caffeine, alcohol, marijuana and opiates prescribed for medication assisted therapy or pain treatment) currently not in remission according to one of the following criteria:
- • Early Full Remission: This specifier is used if none of the criteria for Dependence or Abuse have been met for at least 1 month, but less than 12 months OR
- • Early Partial Remission: This specifier is used if only one or more (but not all) of the criteria for Dependence or Abuse has/have been met for at least 1 month, but less than 12 months. OR
- • Sustained Full Remission: This specifier is used if none of the criteria for Dependence or Abuse have been met at any time during a period of 12 months or longer OR
- • Sustained Partial Remission: This specifier is used if only one or more (but not all) of the criteria for Dependence or Abuse has/have been met for a period of 12 months or longer OR
- • On Agonist Therapy: This specifier is used if the individual is on a prescribed agonist medication, and none of the criteria for Dependence or Abuse has been met for that class of medication for at least the past month (except tolerance to, or withdrawal from, the agonist). This category also applies to those being treated for Dependence using a partial agonist or an agonist/antagonist OR
- • Substance Use Related Disorder (mild) up to two disorders: Patients that are assessed to have mild substance-use-related disorders according to the DSM-V criteria will be allowed to participate in the study as long as the number of the disorder-resulting substances does not exceed two (with the exception of the nicotine, caffeine, alcohol, marijuana and opiates prescribed for medication assisted therapy or pain treatment).
- • 19. History of any seizure disorder.
- • 20. Individuals with history of Guillain-Barré Syndrome.
- • 21. Diagnosis of \>2 Substance Use Related Disorders (mild) based on DSM-V- TR criteria (excluding nicotine, caffeine, alcohol, marijuana and opiates prescribed for medication assisted therapy or pain treatment
- • 22. On a prescribed agonist medication, with criteria for dependence or abuse for that class ofmedication for at least the past month (except tolerance to, or withdrawal from, the agonist
About Weill Medical College Of Cornell University
Weill Medical College of Cornell University is a leading academic institution dedicated to advancing medical research and education. As a prominent sponsor of clinical trials, it focuses on innovative healthcare solutions and the development of new therapies across various medical disciplines. The institution is committed to fostering collaborative research efforts that enhance patient care and improve health outcomes. With a robust infrastructure and a team of experienced researchers and clinicians, Weill Cornell aims to translate scientific discoveries into practical applications, ensuring a strong emphasis on ethical standards and regulatory compliance throughout the clinical trial process.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
Patients applied
Trial Officials
Ronald G Crystal, MD
Principal Investigator
Weill Medical College of Cornell University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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