SBIR-STTR Award

Commercialization of a Diagnostic Test for Amyotrophic Lateral Sclerosis (ALS)
Award last edited on: 4/26/19

Sponsored Program
STTR
Awarding Agency
NIH : NINDS
Total Award Amount
$1,121,400
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Robert P Bowser

Company Information

Iron Horse Diagnostics Inc

21053 N 75th Street
Scottsdale, AZ 85255
   (602) 810-0812
   manager@ironhorsedx.com
   www.ironhorsedx.com

Research Institution

St Joseph's Hospital and Medical center

Phase I

Contract Number: 1R42NS083227-01
Start Date: 9/1/13    Completed: 8/31/14
Phase I year
2013
Phase I Amount
$165,702
Amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease) is a fatal neurodegenerative disease with a typical lifespan of 3 - 5 years after diagnosis. The initial symptoms can be similar to many other neurologic disorders and often begin with limb weakness, muscle fasciculations, or increasing difficulties in speech or breathing. No definitive diagnostic tests currently exist for ALS, and clinical diagnosis typically takes 12 months from symptom onset and relies on ruling out other potential causes of the clinical symptoms. Earlier diagnosis will permit more rapid initiation of treatment with newer drug therapies in development, or equally important provide a means to rapidly rule out ALS as a cause of the symptoms. Iron Horse Diagnostics, Inc. was created to finalize the development of diagnostic and prognostic indicators of ALS and market these assays as laboratory developed tests (LDTs) in a Clinical Laboratory Improvement Amendments (CLIA) certified lab. We have produced a series of peer-reviewed publications convincingly demonstrating that significant levels of pNfH and complement c3 can be detected in the blood and CSF of ALS patients, and that the levels detected by our assays provide diagnostic utility for ALS. We propose a series of tasks to optimize and validate our assays in a CLIA certified laboratory, the last remaining steps before commercialization. This is a FastTrack application because the remaining steps before Phase III are well defined with highly definable go/no-go gates. During Phase I of the proposed work, we will finalize and optimize assays as diagnostic indicators of ALS by testing samples for indicative proteins and translating the assay technology onto a new platform. Phase II will expand on this by conducting a multi-center prospective clinical research study and qualifying the assays using patient samples in a CLIA-certified lab to determine the overall accuracy of the ALS diagnostic. The goal of this proposal is to generate a sensitive and validated LDT (Lab Developed Test) for these biomarkers useful for clinically diagnosing ALS in a CLIA certified lab. A certified LDT will be marketed to clinicians as a service.

Public Health Relevance Statement:


Public Health Relevance:
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that currently lacks a diagnostic test. Iron Horse Diagnostics has cerebrospinal fluid and blood---based diagnostic assays that in our application will be qualified, validated and commercialized as a laboratory developed test (LDT) for ALS.

NIH Spending Category:
ALS; Brain Disorders; Clinical Research; Neurodegenerative; Neurosciences; Rare Diseases

Project Terms:
Age; Amendment; Amyotrophic Lateral Sclerosis; Antibodies; base; Biological Assay; Biological Markers; Blood; Blood specimen; Breathing; Cerebrospinal Fluid; Clinic; Clinical; clinical Diagnosis; Clinical Research; commercialization; Complement; Development; Diagnosis; Diagnostic; diagnostic accuracy; Diagnostic tests; Disease; Early Diagnosis; Enzyme-Linked Immunosorbent Assay; Equipment; Equus caballus; Evaluation; experience; Goals; Immunoassay; Iron; Laboratories; Limb structure; Longevity; Marketing; Measures; Motor; Muscle fasciculation; Muscular Atrophy; nervous system disorder; Neurodegenerative Disorders; Neurologist; neuromuscular; Neuropathy; Paralysed; Patient Care; Patients; Peer Review; Pharmacotherapy; Phase; Production; Prognostic Marker; prospective; Proteins; public health relevance; Publications; Qualifying; Reagent; research study; Sampling; Sensitivity and Specificity; Series; Services; Speech; Symptoms; Technology; Testing; Time; Translating; Work

Phase II

Contract Number: 4R42NS083227-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2014
(last award dollars: 2015)
Phase II Amount
$955,698

Amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease) is a fatal neurodegenerative disease with a typical lifespan of 3 - 5 years after diagnosis. The initial symptoms can be similar to many other neurologic disorders and often begin with limb weakness, muscle fasciculations, or increasing difficulties in speech or breathing. No definitive diagnostic tests currently exist for ALS, and clinical diagnosis typically takes 12 months from symptom onset and relies on ruling out other potential causes of the clinical symptoms. Earlier diagnosis will permit more rapid initiation of treatment with newer drug therapies in development, or equally important provide a means to rapidly rule out ALS as a cause of the symptoms. Iron Horse Diagnostics, Inc. was created to finalize the development of diagnostic and prognostic indicators of ALS and market these assays as laboratory developed tests (LDTs) in a Clinical Laboratory Improvement Amendments (CLIA) certified lab. We have produced a series of peer-reviewed publications convincingly demonstrating that significant levels of pNfH and complement c3 can be detected in the blood and CSF of ALS patients, and that the levels detected by our assays provide diagnostic utility for ALS. We propose a series of tasks to optimize and validate our assays in a CLIA certified laboratory, the last remaining steps before commercialization. This is a FastTrack application because the remaining steps before Phase III are well defined with highly definable go/no-go gates. During Phase I of the proposed work, we will finalize and optimize assays as diagnostic indicators of ALS by testing samples for indicative proteins and translating the assay technology onto a new platform. Phase II will expand on this by conducting a multi-center prospective clinical research study and qualifying the assays using patient samples in a CLIA-certified lab to determine the overall accuracy of the ALS diagnostic. The goal of this proposal is to generate a sensitive and validated LDT (Lab Developed Test) for these biomarkers useful for clinically diagnosing ALS in a CLIA certified lab. A certified LDT will be marketed to clinicians as a service.

Public Health Relevance Statement:


Public Health Relevance:
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that currently lacks a diagnostic test. Iron Horse Diagnostics has cerebrospinal fluid and blood---based diagnostic assays that in our application will be qualified, validated and commercialized as a laboratory developed test (LDT) for ALS.

Project Terms:
Age; Amendment; Amyotrophic Lateral Sclerosis; Antibodies; base; Biological Assay; Biological Markers; Blood; Blood specimen; Breathing; Cerebrospinal Fluid; Clinic; Clinical; clinical Diagnosis; Clinical Research; commercialization; Complement; Development; Diagnosis; Diagnostic; diagnostic accuracy; Diagnostic tests; Disease; Early Diagnosis; Enzyme-Linked Immunosorbent Assay; Equipment; Equus caballus; Evaluation; experience; Goals; Immunoassay; Iron; Laboratories; Limb structure; Longevity; Marketing; Measures; Motor; Muscle fasciculation; Muscular Atrophy; nervous system disorder; Neurodegenerative Disorders; Neurologist; neuromuscular; Neuropathy; Paralysed; Patient Care; Patients; Peer Review; Pharmacotherapy; Phase; Production; Prognostic Marker; prospective; Proteins; public health relevance; Publications; Qualifying; Reagent; research study; Sampling; Sensitivity and Specificity; Series; Services; Speech; Symptoms; Technology; Testing; Time; Translating; Work