Steroid-enhancing Selective Casein Kinase Inhibitors: First In Class Novel Inhaled Anti-asthma Agents
Funder
National Health and Medical Research Council
Funding Amount
$538,064.00
Summary
Chronic lung diseases reduce quality and duration of life of 0.5 billion globally (1 in 4 Australians). Current drugs fail to adequately reduce the decline in lung function. This development is based on the discovery of an enzyme pathway contributing to poor lung function. The project will identify the best doses of the drug and the best combinations with existing drugs to reduce the lung scarring and inflammation. These new findings support efforts to secure investment for clinical testing.
Anticalins: Inhalable Biologicals For Severe Asthma
Funder
National Health and Medical Research Council
Funding Amount
$577,933.00
Summary
This grant aims to develop a new class of medicines called 'anticalins'. Anticalins behave like a successful class of medicines called monoclonal antibodies (mAbs). MAbs are too fragile and large to be inhaled to treat lung disease but anticalins are small and robust. We will be developing an anticalin (PRS-060) which blocks damaging immune reactions in severe asthma. By inhaling PRS-060 we hope to make a new and clinically useful medicine for a common form of poorly-controlled severe asthma.
Novel NLRP3 Inhibitors For Steroid Resistant Asthma
Funder
National Health and Medical Research Council
Funding Amount
$927,117.00
Summary
Asthma causes 40,000 hospitalisations p.a. with 5-10% of asthmatics having severe steroid resistant asthma, a common and debilitating disease, where current treatments do not work. Effective therapies are urgently required. Based on our research, we have novel molecules showing high level of efficacy in models of severe steroid resistant asthma. These molecules will be further investigated to deliver a drug candidate for commercialisation within 3 years.
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.
Evaluation Of The Safety Of Lead Compounds For Allergic Asthma
Funder
National Health and Medical Research Council
Funding Amount
$310,568.00
Summary
Asthma is one of the most common chronic respiratory diseases in developed countries and is typically treated with corticosteroids which provide symptomatic relief and coarse non-specific treatment of the underlying disease. We are pursuing innovative therapies by targeting a different enzyme, HPGD2S, involved in the inflammatory mechanisms of asthma. We have developed potent, anti-inflammatory drug candidates and aim to profile the safety of these compounds before entering clinical studies.
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.Read moreRead less
Prostaglandin D2 (PGD2) is a key driver of asthma and allergic rhinitis. We have developed drug-like compounds that block the synthesis of PGD2 by inhibiting the hematopoietic prostaglandin D2 synthase (HPGD2S) enzyme. This project aims to develop these compounds further to ultimately treat a subset of the asthma population that are not well treated, refractory asthmatics.
Next Generation Hand-held Nebulisers For Aerosol Drug Delivery: Using Microfluidics To Tune Particle Size
Funder
National Health and Medical Research Council
Funding Amount
$726,160.00
Summary
Chronic respiratory diseases (Asthma, COPD) affect 14% of Australians with a greater disease burden felt by elderly and young patients. These patients experience more difficulty administering medication through conventional inhalers due to a lack of coordination and dexterity. We present a patented technology which improves the pulmonary delivery of medication through a microfluidic method, within a system designed specifically to improve user experience and patient monitoring.
This project aims to develop a treatment for hearing loss (none exist) that can be progressed to a clinical trial for patients with significant hearing impairment. The treatment involves the use of drug delivery particles that we have shown to be effective in preventing the loss of sensory auditory cells in deafness. The project will further develop and validate this technology in deafness models so that it can be applied to human patients in a first in human trial.
The Development Of Human Hematopoietic Prostaglandin D2 Synthase Inhibitors In Allergic Asthma And Related Disorders
Funder
National Health and Medical Research Council
Funding Amount
$428,071.00
Summary
Prostaglandin D2 (PGD2) is a key mediator of asthma and allergic rhinitis. We have developed drug-like compounds that block the synthesis of PGD2 by inhibiting the hematopoietic prostaglandin D2 synthase (HPGD2S) enzyme. This project aims to evaluate the potential of these compounds to treat asthma and to further optimize the drug-like characteristics of our lead molecules.