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Research Topic : CLOZAPINE
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  • Funded Activity

    Clozapine-induced Bone Marrow Toxicity: An In Vitro Model For The Study Of Agranulocytosis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $41,072.00
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    Funded Activity

    N-Acetyl Cysteine In Schizophrenia Resistant To Clozapine: A Double-Blind Randomised Placebo-Controlled Trial Targeting Negative Symptoms

    Funder
    National Health and Medical Research Council
    Funding Amount
    $981,789.00
    Summary
    Many patients with schizophrenia remain treatment resistant even after “last resort” medications like clozapine. This proposal will conduct a novel multi-site randomised placebo controlled trial of adjunctive N-acetyl cysteine in patients with clozapine resistant schizophrenia. Treatment efficacy will be examined at 8, 26 and 52 weeks.
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    Funded Activity

    Uncoupled Research Fellowship

    Funder
    National Health and Medical Research Council
    Funding Amount
    $780,307.00
    Summary
    I am a Neuroscientist-Neurologist investigating brain pathways and neurotransmitters controlling body temperature. My research is highly relevant to human physical and mental health.
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    Funded Activity

    Clozapine Toxicity: Role Of Pharmacogenetic Variation In CYP Enzymes And Bioactivation Mechanisms In Patient Neutrophils

    Funder
    National Health and Medical Research Council
    Funding Amount
    $336,000.00
    Summary
    The treatment of mental disorders such as schizophrenia involves the administration of potent drug combinations to patients. Some individuals, however, do not respond to commonly-used antipsychotic drugs and their condition only improves with a unique drug called clozapine. The major problem with clozapine is its toxicity toward blood cells, heart and other organs. All people who receive clozapine must be monitored closely, especially in the first 3-4 months after starting therapy. Several new d .... The treatment of mental disorders such as schizophrenia involves the administration of potent drug combinations to patients. Some individuals, however, do not respond to commonly-used antipsychotic drugs and their condition only improves with a unique drug called clozapine. The major problem with clozapine is its toxicity toward blood cells, heart and other organs. All people who receive clozapine must be monitored closely, especially in the first 3-4 months after starting therapy. Several new drugs have been suggested to be safer versions of clozapine but these are all ineffective. Clozapine is the only agent that is effective in people who do not respond to the other drugs used to treat schizophrenia. Thus, clozapine toxicity, which necessitates discontinuation of the drug, is a devastating outcome because there is no alternative treatment that is available. Another significant problem with clozapine is that its rate of removal from the body is slowed down by many other drugs that are used concurrently. The problems with clozapine occur in some but not all individuals. This suggests that the patient's genetic makeup and their exposure to drugs and environmental agents determine the incidence of toxicity. The present project looks at how clozapine is removed from the body and how it is converted into a toxic product that damages cells. These processes will be examined, with emphasis on differences between individual patients, and strategies to protect cells from damage from the toxic derivative will be tested. Corresponding studies will be done in patients who are receiving clozapine as treatment for psychoses. We will be able to compare experimental and clinical findings in order to identify those patients who appear to be at risk. This will be possible before the toxic effects occur and will help us to identify subjects in whom the drug should only be used with great care. We may also devise strategies that will minimise the incidence of toxicity.
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    Funded Activity

    The Amygdala And Emotionally-mediated Sudden Cutaneous Vasoconstriction In Rats

    Funder
    National Health and Medical Research Council
    Funding Amount
    $461,788.00
    Summary
    Discovering how the brain organizes our emotional life is important for understanding mental illness. In rats, blood flow to the skin falls when the animal detects a possibly dangerous event. Rats go pale with fright , just as humans do. The falls in blood flow are inhibited by drugs used to treat people with schizophrenia. The grant investigates whether the amygdala is an important brain centre controlling the skin blood vessels, and whether anti-schizophrenia drugs act in the amygdala.
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