Mode
Text Size
Log in / Sign up
Phase 2 N=15 Randomized Double-blind Treatment

Therapeutic Cocaine Vaccine: Human Laboratory Study

Cocaine Dependence

Enrolled (actual)
15
Serious AEs
0.0%
Results posted
Dec 2017
Primary outcome: Primary: Cocaine Intoxication — 59; 51; 45; 44 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Cocaine vaccine (TA-CD) (Biological)
Age
Adult · 21+ yrs
Sex
All
Sponsor
New York State Psychiatric Institute
Primary completion
Jul 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Cocaine Intoxication
59; 51; 45; 44; 42; 38
SECONDARY
Cocaine Cardiovascular Effects
75; 82; 92; 79; 98; 109
SECONDARY
Plasma Cocaine
5; 125; 160; 20; 145; 260

Summary

Clinical data demonstrate that a cocaine vaccine (TA-CD: Celtic Pharmaceutical) produces selective anti-cocaine antibodies, yet the impact of these antibodies on cocaine's direct effects is unknown. The objective of this human laboratory study was to measure the relationship between antibody titers and the effects of smoked cocaine on ratings of intoxication, craving and cardiovascular effects. Cocaine-dependent volunteers not seeking drug treatment spend 2 nights per week for 13 weeks inpatient where the effects of cocaine (0, 25, 50 mg) are determined prior to vaccination and at weekly intervals thereafter. Vaccinations occur at weeks 1, 3, 5 and 9.

Eligibility Criteria

Inclusion Criteria

  • Meets DSM-IV criteria for current cocaine dependence. The volunteer may meet criteria for other substance abuse, but not dependence (other than nicotine).
  • Primary route of cocaine administration is smoking.
  • Age 21-45.
  • Females must be surgically sterilized or post- menopausal
  • Able to give informed consent, and comply with study procedures.

Exclusion Criteria

  • Dependence on substances other than cocaine or nicotine.
  • Judged to be noncompliant with study protocol.
  • History of autoimmune disease, immune deficiency or hypersensitivity to other vaccines. An HIV test must be negative.
  • Currently uses drugs intravenously
  • Currently taking any psychotropic medication
  • Laboratory tests that are clinically unacceptable to the study physician (BP > 140/90; BUN, creatinine, LFTs > 1.5 ULN; hematocrit < 34 for women, < 36 for men)
  • Blood or blood products given in the three months prior to vaccination
  • Other vaccines, including flu vaccine, given within 30 days of screening.
  • Ongoing active infection
  • Currently taking immunosuppressives -
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00965263). 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.

Back to search