Amyotrophic Lateral SclerosisLONELYALSNCT07312240
LONgitudinal and Integrated Evaluation of Biomarkers in reLation to phenotYpe in ALS
A study testing Lumbar Puncture for analysis of Cerebrospinal Fluid, Deep Phenotyping and Routine blood chemistry analysis and genetic analysis in people with Amyotrophic Lateral Sclerosis, run by Istituto Auxologico Italiano at 1 site in Italy.
Trial summary
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive degeneration of upper and lower motor neurons, leading to paralysis and death. Despite its uniformly fatal outcome, ALS shows marked clinical heterogeneity with respect to phenotype, progression rate, cognitive involvement… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Amyotrophic Lateral Sclerosis
- What is being tested?
- Lumbar Puncture for analysis of Cerebrospinal Fluid, Deep Phenotyping and Routine blood chemistry analysis and genetic analysis
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 140 participants
- Where
- 1 siteItaly
- Study dates
- 17 Apr 2025to 15 Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- diagnosis of Amyotrophic Lateral Sclerosis (ALS);
- age ≥18 y;
- feasibility of lumbar puncture (LP);
- informed consent.
- age ≥18 y;
- individuals undergoing LP for neurological symptoms;
- no evidence of nervous system pathology;
- informed consent.
Who cannot join
- severe medical comorbidities;
- recent traumatic, inflammatory, vascular, or neoplastic Central Nervous System disease; contraindications to LP.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Italy1 site, 1 recruiting
- Recruiting
Istituto Auxologico Italiano IRCCS
Milan, Lombardy, 20149
Federico Verde, MD, +39-02619111, f.verde@auxologico.it
About this study
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive degeneration of upper and lower motor neurons, leading to paralysis and death. Despite its uniformly fatal outcome, ALS shows marked clinical heterogeneity with respect to phenotype, progression rate, cognitive involvement, and survival. This heterogeneity limits prognostic accuracy and complicates patient stratification in both clinical practice and research settings.
Neurochemical biomarkers have emerged as promising tools to improve diagnosis, prognostication, and understanding of ALS pathophysiology. Among them, neurofilament light chain (NfL) represents the most established biomarker, reflecting axonal degeneration. Additional biomarkers, including glial fibrillary acidic protein (GFAP), phosphorylated tau (p-tau181), and Alzheimer's disease-related markers (Aβ42 and Aβ40), may provide complementary information regarding astroglial activation, motor neuron subtype involvement, and cognitive-behavioral features. However, the phenotypic correlates, longitudinal trajectories, and biological determinants of these biomarkers in ALS are not yet fully understood.
The LONELYALS study is an ongoing, monocentric, observational cohort study with a case-control component, designed to investigate the relationships between ALS phenotype and a comprehensive panel of cerebrospinal fluid (CSF) and blood biomarkers. The study will enroll 140 adult patients with ALS and collect longitudinal clinical, neuropsychological, biological, and laboratory data over a follow-up period of up to 36 months. By integrating biomarker measurements with detailed phenotypic characterization, the study aims to clarify biomarker origins, determinants, and prognostic value, and to identify novel CSF biomarkers relevant to ALS.
Read the detailed description
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting upper and lower motor neurons and leading to muscle weakness, paralysis, and premature death. Although ALS is uniformly fatal, it is characterized by substantial clinical and biological heterogeneity, including differences in site of onset, rate of disease progression, cognitive and behavioral involvement, and survival. This heterogeneity poses major challenges for prognostication, patient counseling, and the design and interpretation of clinical trials.
In recent years, neurochemical biomarkers have gained increasing relevance in ALS research. Neurofilaments, particularly neurofilament light chain (NfL), are currently the most widely studied biomarkers and are considered indicators of axonal degeneration. Elevated NfL levels in cerebrospinal fluid (CSF) and blood have been consistently observed in ALS and are associated with disease severity and survival. However, several key questions remain unresolved, including the relative contribution of upper versus lower motor neuron degeneration to NfL release, the extent to which NfL reflects disease aggressiveness versus anatomical disease burden, and the factors influencing its distribution between CSF and blood.
Other biomarkers may capture complementary aspects of ALS pathophysiology. Glial fibrillary acidic protein (GFAP), a marker of astrocytic activation, has been reported to be increased in ALS and may be related to extra-motor and cognitive features. Phosphorylated tau (p-tau181), widely used as a biomarker of Alzheimer's disease, has recently been proposed as a potential ALS biomarker, possibly reflecting lower motor neuron degeneration. In addition, classic Alzheimer's disease biomarkers such as Aβ42 and Aβ40 may provide insights into cognitive impairment and overlapping neurodegenerative mechanisms in ALS. The relationships among these biomarkers, their longitudinal evolution, and their associations with clinical phenotype and disease progression remain insufficiently characterized.
The LONELYALS study (LONgitudinal and integrated Evaluation of biomarkers in reLation to phenotYpe in ALS) is an ongoing, monocentric, observational clinical-epidemiological study focusing on biological material. The study adopts a prospective cohort design with a case-control component and is conducted at a single specialized ALS center. A total of 140 adult patients with ALS, aged 18 to 90 years, are being enrolled and followed longitudinally for up to 36 months. Patients are recruited during inpatient admissions, and all participants provide biological samples and clinical data according to standardized procedures.
The study involves the collection and analysis of CSF and blood samples, including genetic material, alongside comprehensive clinical, neurological, and neuropsychological assessments. Biomarkers of interest include established and emerging neurochemical markers related to axonal degeneration, astroglial activation, tau pathology, and amyloid metabolism. Longitudinal sampling allows evaluation of biomarker trajectories over time and their relationship with disease progression.
The primary objectives of the study are to explore the associations between baseline biomarker levels and ALS phenotype, to assess the relationships between CSF and blood biomarker concentrations, and to evaluate the prognostic value of biomarkers with respect to longitudinal clinical evolution. Additional aims include investigating the influence of physiological and pathophysiological factors-such as age, sex, body mass index, and renal function-on biomarker levels; exploring interrelationships among different biomarkers; and identifying novel CSF biomarkers relevant to ALS.
By integrating longitudinal biomarker data with detailed phenotypic characterization, the LONELYALS study seeks to improve understanding of ALS pathophysiology and heterogeneity. The results are expected to support biomarker-based patient stratification, facilitate more accurate prognostication, and contribute to the development of personalized clinical management strategies. In the longer term, improved biomarker characterization may also enhance patient selection and outcome assessment in future interventional trials.
- Conditions
- Amyotrophic Lateral Sclerosis
- Being tested
- Lumbar Puncture for analysis of Cerebrospinal Fluid, Deep Phenotyping, Routine blood chemistry analysis and genetic analysis
- Keywords
- Amyotrophic Lateral Sclerosis, Phenotyping, Biomarker
- Medical subject headings
- Amyotrophic Lateral Sclerosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Lumbar Puncture for analysis of Cerebrospinal FluidDiagnostic test
Lumbar Puncture for analysis of Cerebrospinal Fluid for subsequent discovery and validation of a novel biomarker
Deep PhenotypingDiagnostic test
Clinical, neurophysiological, neuroradiological, neuropsychological phenotyping and respiratory investigation
Routine blood chemistry analysis and genetic analysisDiagnostic test
Plasma sampling and genetic analysis
| Study group | Role | What they receive |
|---|---|---|
| ALS Patients | Other | Patients with Amyotrophic Lateral Sclerosis Receives: Diagnostic Test: Lumbar Puncture for analysis of Cerebrospinal Fluid; Diagnostic Test: Deep Phenotyping; Diagnostic Test: Routine blood chemistry analysis and genetic analysis |
| Controls | Other | Individuals undergoing Lumbar Puncture for neurological symptoms but finally having no evidence of nervous system pathology Receives: Diagnostic Test: Lumbar Puncture for analysis of Cerebrospinal Fluid |
What is being measured
The primary outcome is the main question the study is designed to answer.
Clinical - ALSFRS-R score
Measured: At enrolment, at 6 months, at 12 months
Clinical - Penn UMN Score
Measured: At enrolment, at 6 months, at 12 months
Clinical - LMN score
Measured: At enrolment, at 6 months, at 12 months
Neuropsychological phenotyping
Score at Montreal Cognitive Assessment
Measured: At enrollment
Neurophysiological - Limb denervation score (EMG)
Measured: At enrollment
Neurophysiological - CMCT (central motor conduction time) (TMS, transcranial magnetic stimulation)
Measured: At enrolment
Arterial blood gas analysis - PaO2
Measured: At enrollment
Arterial blood gas analysis - PaCO2
Measured: At enrolment
Neuroradiological phenotyping
Presence or absence of T2-FLAIR hyperintensity of the corticospinal tracts
Measured: At enrollment
Neurochemical - Plasma NFL
Measured: An enrolment, at 6 months, at 12 months
Outcome measure for controls
Exclusion of ALS or other neurodegenerative diseases
Measured: At enrolment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Dec 2025
- Study start17 Apr 2025
- Primary completion15 Dec 2027 (estimated)
- Study completion15 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Amyotrophic Lateral SclerosisStudies of the same condition, open and under way.
- More trials run by Istituto Auxologico ItalianoThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 140 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Istituto Auxologico Italiano
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07312240
- Sponsor's protocol ID
- 23A307
- Acronym
- LONELYALS
- Status last verified
- Dec 2025
- First submitted
- 17 Dec 2025
- Last updated
- 31 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- LONgitudinal and Integrated Evaluation of Biomarkers in reLation to phenotYpe in ALS
- ClinicalTrials.gov ID
- NCT07312240
- Acronym / sponsor ID
- LONELYALS / 23A307
- Conditions
- Amyotrophic Lateral Sclerosis
- Keywords
- Amyotrophic Lateral Sclerosis, Phenotyping, Biomarker
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 140 participants (estimated)
- Lead sponsor
- Istituto Auxologico ItalianoUniversity, hospital or other
- Study start
- 17 Apr 2025 (actual)
- Primary completion
- 15 Dec 2027 (estimated)
- Study completion
- 15 Dec 2027 (estimated)
- First posted
- 31 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive degeneration of upper and lower motor neurons, leading to paralysis and death. Despite its uniformly fatal outcome, ALS shows marked clinical heterogeneity with respect to phenotype, progression rate, cognitive involvement, and survival. This heterogeneity limits prognostic accuracy and complicates patient stratification in both clinical practice and research settings.
Neurochemical biomarkers have emerged as promising tools to improve diagnosis, prognostication, and understanding of ALS pathophysiology. Among them, neurofilament light chain (NfL) represents the most established biomarker, reflecting axonal degeneration. Additional biomarkers, including glial fibrillary acidic protein (GFAP), phosphorylated tau (p-tau181), and Alzheimer's disease-related markers (Aβ42 and Aβ40), may provide complementary information regarding astroglial activation, motor neuron subtype involvement, and cognitive-behavioral features. However, the phenotypic correlates, longitudinal trajectories, and biological determinants of these biomarkers in ALS are not yet fully understood.
The LONELYALS study is an ongoing, monocentric, observational cohort study with a case-control component, designed to investigate the relationships between ALS phenotype and a comprehensive panel of cerebrospinal fluid (CSF) and blood biomarkers. The study will enroll 140 adult patients with ALS and collect longitudinal clinical, neuropsychological, biological, and laboratory data over a follow-up period of up to 36 months. By integrating biomarker measurements with detailed phenotypic characterization, the study aims to clarify biomarker origins, determinants, and prognostic value, and to identify novel CSF biomarkers relevant to ALS.
Detailed description
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting upper and lower motor neurons and leading to muscle weakness, paralysis, and premature death. Although ALS is uniformly fatal, it is characterized by substantial clinical and biological heterogeneity, including differences in site of onset, rate of disease progression, cognitive and behavioral involvement, and survival. This heterogeneity poses major challenges for prognostication, patient counseling, and the design and interpretation of clinical trials.
In recent years, neurochemical biomarkers have gained increasing relevance in ALS research. Neurofilaments, particularly neurofilament light chain (NfL), are currently the most widely studied biomarkers and are considered indicators of axonal degeneration. Elevated NfL levels in cerebrospinal fluid (CSF) and blood have been consistently observed in ALS and are associated with disease severity and survival. However, several key questions remain unresolved, including the relative contribution of upper versus lower motor neuron degeneration to NfL release, the extent to which NfL reflects disease aggressiveness versus anatomical disease burden, and the factors influencing its distribution between CSF and blood.
Other biomarkers may capture complementary aspects of ALS pathophysiology. Glial fibrillary acidic protein (GFAP), a marker of astrocytic activation, has been reported to be increased in ALS and may be related to extra-motor and cognitive features. Phosphorylated tau (p-tau181), widely used as a biomarker of Alzheimer's disease, has recently been proposed as a potential ALS biomarker, possibly reflecting lower motor neuron degeneration. In addition, classic Alzheimer's disease biomarkers such as Aβ42 and Aβ40 may provide insights into cognitive impairment and overlapping neurodegenerative mechanisms in ALS. The relationships among these biomarkers, their longitudinal evolution, and their associations with clinical phenotype and disease progression remain insufficiently characterized.
The LONELYALS study (LONgitudinal and integrated Evaluation of biomarkers in reLation to phenotYpe in ALS) is an ongoing, monocentric, observational clinical-epidemiological study focusing on biological material. The study adopts a prospective cohort design with a case-control component and is conducted at a single specialized ALS center. A total of 140 adult patients with ALS, aged 18 to 90 years, are being enrolled and followed longitudinally for up to 36 months. Patients are recruited during inpatient admissions, and all participants provide biological samples and clinical data according to standardized procedures.
The study involves the collection and analysis of CSF and blood samples, including genetic material, alongside comprehensive clinical, neurological, and neuropsychological assessments. Biomarkers of interest include established and emerging neurochemical markers related to axonal degeneration, astroglial activation, tau pathology, and amyloid metabolism. Longitudinal sampling allows evaluation of biomarker trajectories over time and their relationship with disease progression.
The primary objectives of the study are to explore the associations between baseline biomarker levels and ALS phenotype, to assess the relationships between CSF and blood biomarker concentrations, and to evaluate the prognostic value of biomarkers with respect to longitudinal clinical evolution. Additional aims include investigating the influence of physiological and pathophysiological factors-such as age, sex, body mass index, and renal function-on biomarker levels; exploring interrelationships among different biomarkers; and identifying novel CSF biomarkers relevant to ALS.
By integrating longitudinal biomarker data with detailed phenotypic characterization, the LONELYALS study seeks to improve understanding of ALS pathophysiology and heterogeneity. The results are expected to support biomarker-based patient stratification, facilitate more accurate prognostication, and contribute to the development of personalized clinical management strategies. In the longer term, improved biomarker characterization may also enhance patient selection and outcome assessment in future interventional trials.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ALS Patients | Other | Diagnostic Test: Lumbar Puncture for analysis of Cerebrospinal Fluid, Diagnostic Test: Deep Phenotyping, Diagnostic Test: Routine blood chemistry analysis and genetic analysisPatients with Amyotrophic Lateral Sclerosis |
| Controls | Other | Diagnostic Test: Lumbar Puncture for analysis of Cerebrospinal FluidIndividuals undergoing Lumbar Puncture for neurological symptoms but finally having no evidence of nervous system pathology |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (8 listed)
- diagnosis of Amyotrophic Lateral Sclerosis (ALS);
- age ≥18 y;
- feasibility of lumbar puncture (LP);
- informed consent.
- age ≥18 y;
Key exclusion criteria (2 listed)
- severe medical comorbidities;
- recent traumatic, inflammatory, vascular, or neoplastic Central Nervous System disease; contraindications to LP.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Lumbar Puncture for analysis of Cerebrospinal FluidLumbar Puncture for analysis of Cerebrospinal Fluid for subsequent discovery and validation of a novel biomarker | Diagnostic test | ALS Patients, Controls |
| Deep PhenotypingClinical, neurophysiological, neuroradiological, neuropsychological phenotyping and respiratory investigation | Diagnostic test | ALS Patients |
| Routine blood chemistry analysis and genetic analysisPlasma sampling and genetic analysis | Diagnostic test | ALS Patients |
Primary outcome
Clinical - ALSFRS-R score
Time frame: At enrolment, at 6 months, at 12 months
Clinical - Penn UMN Score
Time frame: At enrolment, at 6 months, at 12 months
Clinical - LMN score
Time frame: At enrolment, at 6 months, at 12 months
Neuropsychological phenotyping
Time frame: At enrollment
Score at Montreal Cognitive Assessment
Neurophysiological - Limb denervation score (EMG)
Time frame: At enrollment
Neurophysiological - CMCT (central motor conduction time) (TMS, transcranial magnetic stimulation)
Time frame: At enrolment
Arterial blood gas analysis - PaO2
Time frame: At enrollment
Arterial blood gas analysis - PaCO2
Time frame: At enrolment
Neuroradiological phenotyping
Time frame: At enrollment
Presence or absence of T2-FLAIR hyperintensity of the corticospinal tracts
Neurochemical - Plasma NFL
Time frame: An enrolment, at 6 months, at 12 months
Outcome measure for controls
Time frame: At enrolment
Exclusion of ALS or other neurodegenerative diseases
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Dec 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Lumbar Puncture for analysis of Cerebrospinal Fluid, Deep Phenotyping and Routine blood chemistry analysis and genetic analysis in people with Amyotrophic Lateral Sclerosis, run by Istituto Auxologico Italiano at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 31 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Federico Verde, MD (+3902619111, f.verde@auxologico.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Clinical - ALSFRS-R score (time frame: At enrolment, at 6 months, at 12 months). The study lists 11 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Dec 2025.