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Scheme : Development Grants
Research Topic : TARGETED
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Cancer Therapy (excl. Chemotherapy and Radiation Therapy) (2)
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  • Funded Activity

    Development Of Follistatin As Novel Cancer Therapeutic

    Funder
    National Health and Medical Research Council
    Funding Amount
    $494,324.00
    Summary
    In this project, we aim to rapidly commercialise our discovery that Follistatin, an endogenous hormone, can dramatically improve the efficacy of platinum-based chemotherapy in lung cancer.
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    Funded Activity

    Targeting Ribosomal RNA Transcription With CX-5461 As A New Approach For Treating Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $864,067.00
    Summary
    We have made the fundamental discovery that ribosomal gene transcription is not simply a 'house keeping' process in cancer cells but is required to maintain malignant cell viability. Strikingly inhibition of ribosomal gene transcription using a novel small molecule inhibitor, CX-5461, shows profound selectivity for malignant cells over normal cells. This proposal will translate these observations into 'first in man' phase 1 clinical trials of CX-5461 for the treatment of blood cancers.
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    Funded Activity

    Stability Engineering Of Human Antibody Therapeutics

    Funder
    National Health and Medical Research Council
    Funding Amount
    $421,104.00
    Summary
    Therapeutic monoclonal antibodies are among the fastest growing class of drugs with more than $30 billion sales in 2011. Unfortunately, antibodies often display limited stability and a tendency to aggregate. This greatly hinders their development and results in high failure rates of otherwise promising candidates. We have recently identified mutations that render human antibodies resistant to aggregation. Here we apply this technology to a monoclonal antibody candidate developed by a leading pha .... Therapeutic monoclonal antibodies are among the fastest growing class of drugs with more than $30 billion sales in 2011. Unfortunately, antibodies often display limited stability and a tendency to aggregate. This greatly hinders their development and results in high failure rates of otherwise promising candidates. We have recently identified mutations that render human antibodies resistant to aggregation. Here we apply this technology to a monoclonal antibody candidate developed by a leading pharmaceutical company.
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    Funded Activity

    Harnessing Anticalin Technology As A Multi-targeted Treament Approach For Vision Loss

    Funder
    National Health and Medical Research Council
    Funding Amount
    $627,273.00
    Summary
    Diabetes is a leading cause of vision loss and blindness worldwide and is caused by two factors called VEGF and Ang2, which damage blood vessels. Current treatments only block VEGF and many patients do not respond and suffer irreversible damage to sight. We have used ground-breaking anticalin technology to make a new drug (PRS-AUS1) that blocks both VEGF and Ang2. Studies will be performed in animal models and move to patients where we expect improved outcomes compared to current treatments.
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    Funded Activity

    Achieving Targeted Delivery Of Drugs To Uterine Muscle In Women For The Prevention Of Preterm Labour

    Funder
    National Health and Medical Research Council
    Funding Amount
    $469,008.00
    Summary
    We have patented liposomes targeted to the uterus, which enable us to deliver drugs specifically to the muscle cells of the uterus, increasing safety. The liposomes can be loaded with drugs that either block or promote contractions, creating a versatile drug delivery system that could treat premature labour or postpartum haemorrhage which are major clinical problems. We seek support to demonstrate their effectiveness in mouse and primate models of preterm labour prior to human studies.
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    Funded Activity

    Preclinical Development Of A Therapeutic Anticancer Antibody To C-Met

    Funder
    National Health and Medical Research Council
    Funding Amount
    $435,530.00
    Summary
    Many common cancers cannot be effectively treated. A range of these cancers (e.g. gastric and lung cancer) display the molecule c-Met on their cell surface. c-Met promotes tumour growth; therefore, blocking c-Met is a promising strategy for treating these cancers. However, no antibodies or drugs that target c-Met have been licensed. The therapeutics that are being developed to target c-Met all have considerable limitations. Thus, there is an opportunity to develop a 'best-in-class' therapeutic.
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    Funded Activity

    Development Of A Novel MicroRNA Mimic For Cancer Treatment

    Funder
    National Health and Medical Research Council
    Funding Amount
    $534,179.00
    Summary
    Liver cancer is a major health burden globally, with a very poor prognosis. New treatments are urgently needed. We have developed proof-of-concept data showing that a tiny RNA, called a microRNA, is a powerful inhibitor of liver cancer growth. We will use this grant application to further develop the microRNA with novel chemistry so that it can be readily translated into early phase clinical trials in the near future.
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    Funded Activity

    Sortase Peptide Technology: Enzymatic Site-specific Bioconjugation To Improve Antibody Drug Conjugate Production And Performance

    Funder
    National Health and Medical Research Council
    Funding Amount
    $402,046.00
    Summary
    Cancer is characterised by uncontrolled cell growth, leading to invasion and destruction of adjacent tissues. It is a major cause of death in Australia. Targeted drug delivery is an attractive therapeutic strategy that has the potential to lower systemic drug concentrations and reduce side effects. We are developing more efficient cancer drugs.
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    Showing 1-8 of 8 Funded Activites

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