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Strategy

    Identify new mechanisms and molecules to selectively kill cancer and infectious organisms

    • - Collaborate/partner to optimize and evaluate the molecules preclinically as potential medicines
    • - Provide/partner these molecules/assets to organizations that can develop them into medicines


    Develop and implement platforms and tools/assays to identify effective molecular mechanisms of action

    • - Make tools and platforms available for collaboration and fee for service
    • - Identify pharmacological link between gene and patient



iRND3 discovery strategy


Learn and confirm cycle of drug discovery and development

iRND3 focus is on the discovery phase (green). The approval of a medicine to treat an unmet medical need involves an iterative cycle of testing and learning. This figure describes some of the important phases in the process.

The process of discovery and development of a new medicine is initiated in response to an unmet medical need to treat a disease. Physiological, genetic and chemical knowledge provide an understanding of the disease. This knowledge will lead to the identification of translation biomarkers that are used to evaluate the effectiveness of a potential medicine. The available knowledge informs drug discovery strategies which are used as starting points for the practical process of discovering a new medicine.

iRND3 uses this knowledge to inform its lead discovery strategies. The lead discovery strategies are used to identify new medicine candidates. A candidate molecule will then be tested for proof of concept in predictive models of disease. The candidates that are effective in the disease models will be optimized for biopharmaceutics properties and safety to provide a drug candidate ready for clinical studies in humans.

The left hand of the circle (from 6 to 12 o’clock) is the development phase of drug discovery which involves testing for safety and efficacy in humans leading to registration. Multiple iterations are generally required before a medicine with sufficient efficacy at a safe dose is discovered, tested in humans and registered.


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