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Investigation of the Drug Dimethoxbenzylidene Anabaseine in Treating Schizophrenia Patients

Phase 1 Trial of 3-2,4 Dimethoxbenzylidene Anabaseine in Schizophrenia

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00255918
Enrollment
12
Registered
2005-11-21
Start date
2004-03-31
Completion date
2005-10-31
Last updated
2015-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychotic Disorders, Schizophrenia

Keywords

Evoked Potentials, 3-(2,4-dimethoxybenzylidene)anabaseine, DMXB-A, Receptors, Nicotinic

Brief summary

This study will determine the effectiveness of a drug, dimethoxbenzylidene anabaseine, in producing beneficial effects similar to that of nicotine in individuals with schizophrenia.

Detailed description

Schizophrenia is a chronic and severe brain disorder that can significantly impact quality of life. It is characterized by delusions, paranoia, and disordered thinking. The cause of schizophrenia has not yet been determined. However, there are many treatments, including drug therapy and cognitive behavioral therapy, that may help to alleviate symptoms of the condition. Nicotinic receptors are involved in a number of biological processes; they are numerous throughout the central and peripheral nervous systems and are diverse in structure and expression. Genetic and neurobiological research has identified decreased expression of the a7 nicotinic receptor as an element in schizophrenia that is related to poor psychosocial outcome. Data indicate that drug therapy may reduce this deficit in receptor expression. Nicotine has been found to stimulate the a7 nicotinic receptor; however, the physiological dependence associated with nicotine makes it an undesirable option. Dimethoxbenzylidene anabaseine (DMXB-A) can stimulate the a7 nicotinic receptor; its advantages include easy oral administration and the lack of dependence-causing effects. This study will determine whether DMXB-A can safely and effectively stimulate the a7 nicotinic receptor in schizophrenia patients and reduce their neurobiological symptoms. This study will last 6 weeks. Participants will have study visits each week for the duration of the study. During each visit, participants will be randomly assigned to receive either DMXB-A or placebo. An electrocardiogram (EKG) will measure the heart function of participants and participants' blood pressure will be measured. After the first dose of either DMXB-A or placebo, participants will receive a second dose 2 hours later. An evoked potential test, which measures the brain's response to stimuli, will be performed after both doses. Neuropsychological tests, such as verbal reasoning and visual retention, will be performed following the second dose of either DMXB-A or placebo.

Interventions

DRUGDimethoxybenzylidene anabaseine (DMXB-A)

DMXB-A 150 mg immediate release followed by DMXB-A 75 mg 2 hours after the intiial dose

DRUGPlacebo

Placebo dosed to match active medication

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of schizophrenia

Exclusion criteria

* History of cardiovascular illness or neurological illness other than schizophrenia * Current substance abuse, including nicotine * History of clozapine use

Design outcomes

Primary

MeasureTime frameDescription
Total Scale Score for the Repeatable Battery for the Assessment of Neuropsychological StatusMeasured at 2 hours after drug or placeboten subtests which give five scores, one for each of the five domains tested (immediate memory, visuospatial/constructional, language, attention, delayed memory).

Secondary

MeasureTime frameDescription
Brief Psychiatric Rating ScaleMeasured 4 hours after drug or placebo administrationBrief Psychiatric Rating Scale (BPRS) is a rating scale used to measure psychiatric symptoms
P50 auditory evoked potential test amplitude/conditioning amplitude ratioMeasured 2.5 hours after drug or placebo administrationThe evoked response amplitude measured in mV to the initial auditory stimulus which is compared to the evoked response amplitude which is measured in mV to a second auditory stimulus that occurs 500 ms later.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026