FightMND invests $20.2M in the fight against MND in 2023

FightMND will invest a further $20.2 million into Motor Neurone Disease (MND) research to find better treatments and a cure.

Of this years total, over $16.54 million will be committed to vital MND research projects identified through FightMND’s competitive grant round.

Twenty-three exciting new projects will be supported including one clinical trial, seven drug development projects and four projects that will focus on identifying the cause/s of MND.  Seven innovative projects will tackle some of the biggest hurdles in MND, such as the delay in diagnosis.

In addition, six outstanding researchers have been awarded scholarship and fellowship funding in this year’s grant round and will commit the next four years of their careers to battling the disease in research labs and clinics.

The gene that put Australia on the map for MND research 

In March 1993, SOD1 was the first gene linked to MND with the help of Nigel Laing and a team of Australian researchers in WA. As a student at the time, and now a research professor in the MND field, Anthony Akkari witnessed the impact the discovery made in MND research. 

Anthony remembers Professor Laing investigating the inheritance patterns in a large West Australian family affected by MND and a discussion with Professor Laing about MND: “It was that particular conversation, on that day, that engaged me as a student, curious and driven to research this inherited MND,” said Anthony. “Later that same year, my own father was diagnosed with MND; these two events turned me into both a neuromuscular disease researcher and carer for someone with MND.” 

For Anthony, the history of the SOD1 gene discovery as a cause of MND highlights the strides made in MND research by Australian researchers. “Australia’s MND researchers have always had a view beyond the horizon when working to advance the understanding of MND.” 

Professor Akkari has penned an article on the discovery, to access please click the link below.

$84.88M invested into vital MND research since 2014

Thanks to our supporters, FightMND is now one of the world’s largest independent funders of MND research.

By funding the best, high-quality research and connecting the world’s most innovative MND minds, FightMND is playing a lead role in the global fight to find a cure for this devastating disease

We work closely with other relevant MND bodies, taking a lead role in new drug development and clinical trials and doing so with a sense of urgency on behalf of all Australians currently fighting MND.

We have now invested more than $84.88 million into research projects and initiatives since we began in 2014.

2022 CLINICAL TRIALS

Phase 3 Clinical Trial – Randomised double-blind placebo-controlled Phase 3 trial of Lithium Carbonate in MND, a sub-study of a Multi-arm, Adaptive, Groupsequential trial NETwork to evaluate drug
efficacy in patients with MND (MAGNET).

Professor Matthew Kiernan
The University of Sydney, NSW

Phase 2 Clinical Trial – A placebo-controlled safety and efficacy of ambroxol in individuals with MND,

Associate Professor Bradley Turner
The Florey
The University of Melbourne, VIC

2022 DRUG DEVELOPMENT PROJECTS

Drug Development projects are focused on advancing promising new drugs or therapies through the final stages of testing in preparation for their assessment in clinical trials with MND patients. In 2021, FightMND awarded 5 Drug Development projects.

1. THERAPIES TARGETING MUSCLE

Intramuscular allosteric agonism of purinergic P2X7 receptor as a pharmacological approach to enhance skeletal muscle regeneration in MND

Dr Giovanni Nardo
Mario Negri Institute for Pharmacological
Research, Italy

2. TREATMENTS TARGETING MULTIPLE CAUSES OF MND

Validation of the clinical-stage drug candidate RRx-001 as a novel disease modifying therapeutic for MND.

Dr Tony Reid
EpicentRx, Inc., California, USA

2022 DISCOVERY PROJECTS

1. GENETIC AND ENVIRONMENTAL INTERACTIONS

Epidemiology in a dish: using human iPSC to discover common and genotype specific molecular signatures of the multistep hypothesis of MND.

Associate Professor Anthony Cook
University of Tasmania, TAS

2. RESCUING THE BLOCKAGE OF CRITICAL FUNCTIONS IN MOTOR NEURONS CAUSED BY GENE DEFECTS

Trouble at the ribosome in C9ORF-72-driven MND

Dr Danny Hatters
The University of Melbourne, VIC

3. CHANGES IN THE FUNCTION OF CELLS IN THE BRAIN AND SPINAL CORD THAT NORMALLY SUPPORT MOTOR NEURON HEALTH

Multiomic interrogation of patient-derived neurotoxic glia

Dr Jeffrey Liddell
The University of Melbourne, VIC

2022 COLLABORATIVE INITIATIVES PROJECTS

1. MND BIOMARKER PROGRAM

Pre-familial and early MND biomarker program

Associate Professor Mary-Louise Rogers
Flinders University, SA

2. MND BRAIN IMAGING INITIATIVE

AMII: Asia-pacific MND Imaging Initiative

Dr Sicong Tu
The University of Sydney, NSW

2022 IMPACT PROJECTS

1. GENE THERAPY/DRUG DELIVERY

Enhanced neuronal delivery, gene targeting and neuroprotection: development of a multimodal drug against MND

Dr Loren Flynn
Murdoch University, WA

2. GENE THERAPIES

Targeted degradation of misfolded TDP-43 as a therapy for MND

Dr Luke McAlary
The University of Wollongong, NSW

3. DISEASE MODELS

Advanced modelling of upper motor neuron MND pathology using human pluripotent stem cells

Professor Clare Parish
The University of Melbourne, VIC

4. DISEASE MODELS

Evaluation of a novel inducible muscle specific TDP-43 mouse model of MND

Professor Aaron Russell
Deakin University, VIC

5. GENE THERAPIES

Therapeutic targeting of TDP-43 through selective reduction of ataxin-2 expression with peptide-conjugated antisense oligonucleotides

Dr Fazel Shabanpoor
The University of Melbourne, VIC

6. PAUL FISHER IMPACT GRANT – DISEASE HETEROGENEITY

RNA-binding proteins involved in the pathogenesis and disease heterogeneity
of sporadic MND

Dr Rachel Tan
The University of Sydney, NSW

7. DISEASE MODELS

Developing a validated C9orf72 mouse model of ALS/FTD using genome editing MND

Associate Professor Bradley Turner
The University of Melbourne, VIC

8. DISEASE MODELS

New viral-mediated TDP-43 mouse models of MND

Dr Adam Walker
The University of Queensland, QLD

9. DISEASE MODELS/DRUG DELIVERY

Development of a human MND Neurovascular Unit model to improve therapeutic translation in drug testing

Associate Professor Anthony White
QIMR Berghofer Medical Research
Institute, QLD

10. DISEASE HETEROGENEITY/DISEASE BIOMARKERS

Profiling monocytes in MND to assess disease progression and heterogeneity

Professor Trent Woodruff
The University of Queensland, QLD

2022 FELLOWSHIPS

1. BILL GUEST MID-CAREER RESEARCH FELLOWSHIP

The Bill Guest Mid-Career Research Fellowship is named in recognition of the extraordinary contribution of Bill Guest AM, the inaugural Chairman at FightMND.

Dr Adam Walker – Bill Guest Mid-Career Research Fellow
The University of Queensland, QLD

PROJECT:
Clearing TDP-43 pathology for MND therapy

2. MID-CAREER RESEARCH FELLOWSHIP

Dr Rachel Tan
The University of Sydney, NSW

PROJECT:
Reversing TDP-43 pathology and neuronal loss in sporadic MND

3. EARLY CAREER RESEARCH FELLOWSHIP

Dr Taide Wang
The University of Melbourne, VIC

PROJECT:
Therapeutic targeting of ferroptotic cell death in MND

Dr Taide Wang was also the inaugural recipient of the Angie Cunningham Scholarship.

FOR RESEARCHERS – 2024 RESEARCH FUNDING

As the largest independent funder of MND/ALS research in Australia, FightMND’s vision is a world without MND. Integral in this vision is our determination to help facilitate the translation of the growing body of new knowledge about the disease into treatments and ultimately a cure for MND/ALS patients internationally. FightMND’s 2024 grant round opens on November 2 2023 with funding opportunities for both national and international researchers through a number of research schemes.

 

Join the fight,
donate today

Donate Now

2021 DRUG DEVELOPMENT PROJECTS

1. Preventing neuroinflammation in MND by inhibiting the mPTP

A/Prof Seth Masters
(WEHI, VIC)

2. Alpha 5 Beta 1 Integrin as a potential treatment for MND

Prof Lawrence Steinman
(Alpha 5 Integrin LLC, CA, USA)

3. Developing a monoclonal antibody modulating CD38 against MND

Dr Damien Toulorge
(ENCEFA, France)

4. Targeting misfolded proteins with misfoldUbLs as a therapeutic strategy for MND

Prof Justin Yerbury
(University of Wollongong, NSW)

5. Targeting CK1e-mediated TDP-43 Phosphorylation in MND

Dr John Ravits
(University of California – San Diego, CA, USA)

2021 IMPACT PROJECTS

To accelerate the development of effective therapies for MND, FightMND IMProving and ACcelerating Translation (IMPACT) grants support projects focused on overcoming one or more key barriers preventing the advancement of potential treatments through to clinical trial. In 2021, FightMND awarded 10 IMPACT grants to support projects dedicated to accelerating promising research discoveries through to the clinic.

1. Disease biomarkers – Generating a proteomics-based biomarker for MND

Dr Allan McRae
(University of Queensland, QLD)

2. Disease biomarkers – EC-FUS – A novel biomarker for MND examined using a unique antibody

Prof Julie Atkin
(Macquarie University, NSW)

3. Disease biomarkers – The Glymphatic System: A novel biomarker of disease severity in MND

A/Prof David Wright
(Monash University, VIC)

4. Disease heterogeneity – Exploiting cryptic relatedness in global MND to uncover disease- and phenotype-linked genes

Dr Kelly Williams
(Macquarie University, NSW)

5. Disease heterogeneity – Developing a high-throughput system to identify MND risk genes

Dr Fleur Garton
(University of Queensland, QLD)

6. Disease heterogeneity – Identifying novel structural variations in MND genes to improve clinical trial outcomes

Prof P. Anthony Akkari
(Perron Institute for Neurological and Translational Science, WA)

7. Gene therapies – Restoring autoregulation of TDP43 in MND using splice-switching antisense oligonucleotides

A/Prof Lezanne Ooi
(University of Wollongong, NSW)

8. Drug delivery/Gene therapies – Enhancing delivery of gene therapy to motor neurons and glial cells using focused ultrasound

Dr Kara Vine
(University of Wollongong, NSW)

9. Regenerative medicine – Subpial spinal cord delivery as a stem cell-based treatment for MND

A/Prof Lachlan Thompson
(University of Melbourne, Florey, VIC)

10. Disease models – Harnessing phase separation as a preclinical strategy for the treatment of MND

Dr Marco Morsch
(Macquarie University, NSW)