PROJECT TRYMe

 

 

PROJECT TRYMe: An International Collaboration to find Effective Treatments for Motor Neuron Disease

Amyotrophic Lateral Sclerosis (ALS), also known as Motor Neurone Disease (MND) is a fatal neurodegenerative disease that strikes in midlife and kills one person every 2 days in Ireland.  People with MND experience rapidly progressive and ultimately fatal decline in their ability to move their muscles, to speak and to swallow. Half of those affected by MND experience decline in their ability to process information and to manage their behaviour.

We now know that MND overlaps with other more common brain conditions including dementia and schizophrenia. 

There is no effective treatment for MND.  Despite huge investment over the years in animal models of MND, we have not yet succeeded in translating successful treatments to humans.  In the past 15 years, over 45 clinical trials of new treatments in human have failed, costing hundreds of millions of euro. This is because human MND  is more than one condition, but our clinical trials have not reflected this.  

It is time to move to a new precision-medicine based approach towards treatment.

To achieve this we need a radical change in how we engage in research.  MND is a human disease. We must shift the focus from animal research to human research. We will not find new treatments without working together and investing in the study of people with the disease. 


European MND Centres must join forces to capitalize on our individual strengths, and to build on new and creative approaches that enhance our collective scientific expertise.  It is also imperative that we include those who are experiencing the disease first hand.


By working together, we have a better chance of succeeding in our shared goal to find a treatment for MND.  Project TryMe is a new international initiative that will focus only on the human form of the disease.  We need those with MND to work with us, so that we can try to find new treatments together.

The objective of Project TryMe is to have the right drug in the right dose, for the right patient at the right time.  
The best way to achieve this is for researchers to study the human condition.

Centres of MND  research in Ireland, Holland, the UK, France, Belgium and Italy, working at the highest international level, have joined in the Project TryMe campaign.  Each centre has cutting edge skills and scientific expertise in MND that will contribute to our goal of a precision medicine-based approach towards new treatments for MND. The Project TryMe campaign will raise funds for specific research initiatives that will enhance and share this expertise across sites.

An important obstacle to finding new treatments for MND has been our incomplete understanding of genetic factors. Project MinE (www.projectmine.com) was designed to address this. 
Project MinE is a crowd funded initiative, in which 13 partner countries have raised funds to support genome sequencing of DNA samples from their own population.  Project MinE is achieving its goals by analysing the genetic code of 15,000 MND patients and 7,500 healthy people in exquisite detail to discover every gene that contributes to MND  risk.


Having raised €1.6 million, the Irish arm of Project MinE based in Trinity College Dublin has contributed DNA samples of 700 MND patients and 350 healthy participants to the project.  


Project MinE has already made many important discoveries that are reshaping our understanding of MND and has taught us that there are many subtypes with distinctive characteristics. Each subgroup of patients is likely to require a different treatment.  


But Genetics is only part of the story. We also need to focus on how the disease manifests in individual patients.  We need to combine our collective clinical studies with our new genetic insights to have a true Precision Medicine approach towards new treatments.  


Project TryMe will combine the genetic information from Project Mine with innovative approaches towards disease categorization, using shared methods developed by individual partners within the Project TryMe consortium. These additional cutting-edge methods include novel approaches towards epidemiology, clinical assessment, neuropsychology and behavioural assessment, biochemical measures, MRI, and brain signal analysis and measurements of patient outcome.  
European Researchers in Project TryMe will combine all of  these approaches to identify new ways for grouping patients into different clusters, and to develop new and more cost-effective ways of testing new drugs.   


This will allow us to enroll groups of patients in new clinical trials that are specifically targeted towards their type of disease. 

Ireland has excelled in patient categorization for many years.   
Our work capitalizes on the natural research strengths within the Irish population (epidemiology and genetics) and scientific expertise within the MND Research Group at Trinity College Dublin.
Our contribution will be in 7 thematic areas, outlined in detail in the attached Appendix:

  • Genetics
  • Epidemiology
  • Cognition
  • Imaging
  • Signal Analysis
  • Outcome measures
  • Patient and Caregiver Ecosystem

Appendix: Detailed of the Irish Research Contribution to Project TRYMe

The Irish MND Research Group has a strong track record in genetics research, including the identification of a new causative gene in MND in 2006, and contributions to 3 new genes in the past 18 months. Genetics research has developed considerably over the past 3 -5 years and requires highly trained statisticians and bio-informaticians to analyses the trillions of data points generated from genomic sequencing.  

As part of the Project Mine initiative (www.projectMinE.com) , we will continue to  engage in detailed analysis of Irish MND genetics, using state of the art bioinformatics technology, in collaboration with colleagues in the Smurfit Institute of Genetics TCD. (Funding for genomics has been generated from the Project Mine initiative)

Deliverables:

  • Identification of new susceptibility genes in MND
  • Identification of genes that “travel together” (oligogenic inheritance)
  • Identification of gene interactions that contribute to ALS 
  • Identification of new pathways for drug development
  • Genetic Association between MND and Schizophrenia
  • Characterization of the genetic profile of the Irish population

5-year cost:   This project is funded from Project MinE

The Irish Register of MND captures and verify all new patients who have consented to their inclusion on the Register.  It is the longest running Register of its kind in the world, and is internationally recognized as a 'gold standard'. 

This resource permits continued collection of information about lifetime exposures from people with MND and recruitment matched controls as part of our international collaboration with colleagues in Holland and Italy as part of the ENCALS network (www.ENCALS.com)

Each person with MND is asked for detailed information about their employment and recreational history. We also collect information about family history, and we are currently exploring the hypothesis that those with a strong family history of other related neurological and neuropsychiatric conditions harbour susceptibility genes that may contribute to both MND and other neurological/neuropsychiatric conditions. DNA is used to look for these “at risk” genes, and to determine how they interact with environmental exposures.

Deliverables from the theme:

  • Continuation of the Irish Register, inclusion of high quality verified data, and regular quality control analysis.
  • 2,300 individuals have been included on the Register to date. Family aggregation studies have shown that the familial rate of MND in Ireland is 30%.
  • Exposures that are likely to increase the risk of developing MN
5 year Cost:  Register Manager:  €80,000 per annum
  Epidemiologist:  €90,000 per annum
  Statistician:  €90,000 per annum

Using the Irish Register and population-based controls, we are characterizing the cognitive and behavioural profile of MND patients in Ireland and are studying the neuropsychiatric and neurobehavioral conditions in families of people with MND using a previously described semi- structured interview, chart review and death certification. All patients and controls provide a DNA sample as part of our study of genetic and environmental factors in MND. Control kindreds are selected based on age, gender and educational status of the MND patients, and undergo similar analyses. Index patients and first-degree relatives are invited to participate in a detailed study using a previously used standardized neuropsychological battery including extensive assessment of cognitive and behavioural status and social cognition, and neuroimaging using standardized structural and functional protocols.    The aim of this work is to identify families that are likely to harbour genes that can contribute to both neurological and neuropsychiatric conditions.
DNA from these families is sequenced to identify previously unknown genes that contribute to disease susceptibility.

Deliverables

  • Definition of cognitive and behavioural subtypes in MND
  • Improved stratification of clinical trials
  • Improved targeting of drugs to patient sub-cohorts
  • Characterization of the clinical, behavioural and cognitive sub-phenotypes of MND
5 Year Cost:  Senior Neuropsychologist: €100,000 per annum
  Research Assistants:  €100,000 per annum

The aim of this work is to develop non-invasive imaging modalities into accurate diagnostic, prognostic and monitoring of the changes in the brain in MND. The findings have implications for diagnostic applications, clinical management, pharmaceutical trials, and characterising anatomical patterns of pathological spread in neurodegeneration. The theme leader in imaging, Dr Peter Bede collaborates the Signal Analysis Theme Group, led by Dr Bahman Nasseroleslami. This exciting work will help us to find better and more reliable markers of disease onset, progression and subgroup categorization, in MND, and has enormous potential as a biomarker of future clinical trials.

Deliverables

  • Early and accurate diagnosis of MND
  • Identification of selective regions of degeneration that correlate with changes in neuropsychology and EEG
  • Identification of subgroups of MND for new clinical trials in MND.
Research Costs: Research Scientist:  €70,000 per annum
  Clinician Scientist:  €90,000 per annum
  Imaging costs:  €100,000 per annum

There is evolving evidence that MND is cause by disintegration of networks of nerves, rather than death of individual nerve cells. We believe that the failure of translation of drugs from animals to humans is likely due to the complexity of neural networks in humans, which are disrupted in diverse ways (disease heterogeneity).


The purpose of this research theme is to change how we look at MND based on the dysfunction levels in several specific neural networks.
Work in Trinity College Dublin is at the forefront of this type of signal analysis in the brain of those with MND.  The theme leader is a Neural Engineer (Dr. Bahman Nassereloslami). 


The group is developing novel and inexpensive ways to separate patient groups based on differential types of network disruption. We collect brain waves (EEG) during resting-state to identify which networks are disrupted. We then study networks by EEG during thinking tasks, and movement-related networks by activating the motor nerves within the brain by a non-invasive device (magnetic stimulation). We correlate these measures with results from neuropsychological tests of thinking and behaviour, and with changes in MRI, and will use these new tools as biomarkers that will help to separate patients into different subgroups, and that can be used to measure disease progression over time in clinical trials.

Deliverables

  • Identification of early differences in brain networking – improving diagnoses
  • Identification of subgroups with different patterns of network disruption that respond to different drugs
  • Tracking disease progression in clinical triMND and improving quantitative outcomes
  • Finding better ways to measure thinking and behavioural changes by identifying the patterns of network disruption
Research Costs: Senior Neural Engineer:  € 120,000 per annum
  Research Scientist    € 60,000 per annum
  Clinician Scientist:  €80,000 per annum

This work is focused on the decreased functional ability in walking ability (gait) hand function (dexterity), swallowing, and speech that occurs in MND.  The theme leader (Dr. Meldrum, and main researcher (Dr. Murray) are both academic physiotherapists who have recently joined the MND Research Group.  Their theme relates to the development of better outcome measure for clinical trials.

The objective in clinical trials is to measure the effect of a compound on functional ability by determining whether it can slow down or stop the rate of neurological decline. But detection of meaningful change requires reliable quantitative outcome measurements, and most of scales used for clinical trials are semi- qualitative. This means they attribute a numerical value to a clinical assessment by an examiner. Because clinical examination can be very variable, conversion of the clinical findings to a rigid ordinal scale introduces problems with reliability and variance, which increases the risk of failure to identify a real effect of a new drug. Also, most scales do not provide a "clinical meaningfulness" measurement. We have no way of determining the real-life impact of a drug, because we cannot convert the numerical outcome measurement into how functions of everyday life.   We are developing sensitive non-subjective tests to resolve the problems of variance in the outcome measure for MND (the ALSFRS-R).

Deliverables

  • Quantitative outcome measures using novel devices
  • Better and more accurate outcome measures for clinical trials
  • Definition of clinical meaningfulness of a drug.
Research Costs: Senior Clinician Scientist (Physiotherapist):  €90,000 per annum
  Research Scientist:     €60,000 per annum
  Research Engineer:     €60,000 per annum

We are tracking the patient journey from diagnosis to end of life to understand the entire cost from a financial perspective. We are also studying the effect of the illness on the family “ecosystem”, by engaging with patients and carergivers determine quality of life, caregiver burden and palliative care needs.

Along with physical decline, thinking and behaviour changes are significant factors that contribute to caregiver burden in MND and there is evolving evidence that caregivers’ psychological status may also influence the mental and physical outcome of patients. However, the presence of cognitive/behavioural changes in MND is often under-recognized by healthcare professionals and the burden of care associated with these changes is not addressed. We are investigating the consequences of cognitive and behavioural effects on caregiver burden in MND

We achieve this through assessment of objective and subjective caregiver burden using both structured and semi-structured interview techniques. We are developing a rational approach to enable self-management of burden and develop guidelines for health care professionals to recognize cognitive and behavioural change in MND and the associated burden for caregivers.

Deliverables

  • Total Cost of MND
  • Whole illness model of MND
  • New tools to measure the impact of a new therapeutics on the patient journey, for the purposes of health technology assessment
  • New interventions to limit caregiver burden
Research Costs: Senior Research Scientist: €90,000 per annum
  Research Assistants (x3): €90,0000 per annum
  Health Economist:   €60,000 per annum   

 

TOTAL COSTS (including estimated annual increments)

 

 

YEAR 1

YEAR 2

YEAR 3

YEAR 4

YEAR 5

TOTAL €

 

THEME 1

FUNDED

THEME 2

260,000

270.000

280,000

290,000

300,000

1,400,000

 

THEME 3

200,000

210,000

220,000

230,000

240,000

1,100,000

 

THEME 4

260,000

270,000

280,000

290,000

300,000

1,400,000

 

THEME 5

260,000

270,000

280,000

290,000

300,000

1,400,000

 

THEME 6

210,000

220,000

230,000

240,000

250,000

1,150,000

 

THEME 7

240,000

250,000

260,000

270,000

280,000

1,300,000

 

RESEARCH MANAGER

90,000

95,000

100,000

105,000

110,000

500,000

 

 

 

 

 

 

 

 

 

TOTAL

1,520,000

1,585,000

1,650,000

1,715,000

1,780,000

8,250,000