Motor Neurone Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are willing to take part, have been fully informed about the study, and agree to sign a consent form and follow all study procedures.
- You are between 18 and 80 years old (any gender), and if you are 18 or older with ALS, you weigh more than 40 kilograms (about 88 pounds).
- You have been diagnosed with ALS (Amyotrophic Lateral Sclerosis) according to specific 2020 diagnostic guidelines called the "Gold Coast Criteria," at a "confirmed" or "probable" level.
- Tests (clinical, nerve, or tissue tests) show signs that the lower part of your nervous system's motor pathways is affected.
- You score 1 or higher on a frailty assessment scale called the Frailty Phenotype scale (confirm with trial site).
- Other diseases have been ruled out as the cause of your symptoms.
- You agree to provide blood, stool, and urine samples during the study for research purposes.
Who may not be able to join:
- You have another neurological condition with symptoms similar to ALS, such as neck or back spine problems or dementia.
- You have an autoimmune disease such as Multiple Sclerosis, Rheumatoid Arthritis, Lupus, Myasthenia Gravis, or similar conditions.
- Your kidneys are not working well enough (based on a specific kidney function test result below a certain level).
- Your liver is significantly damaged, shown by abnormal liver blood tests or a known liver condition such as hepatitis or cirrhosis.
- You have a serious lung condition such as COPD or pulmonary fibrosis.
- You have had a heart attack or a heart procedure in the last 6 months, or you have moderate-to-severe heart failure.
- You have another serious disease affecting your nervous system, heart, lungs, blood, hormone system, or you have a serious mental illness.
- You have a known or suspected history of alcohol or drug abuse.
- Your expected survival is 3 months or less.
- You are pregnant, breastfeeding, or planning to become pregnant, or you are unwilling to use effective contraception from the start of the study until 3 months after stopping the study medication (this applies to both women and men whose partners could become pregnant).
- You are known to be allergic to any ingredients in the trial treatment, or you have a history of serious allergic reactions.
- Researchers believe you may misuse the study drugs in a way that could affect the results.
- You have any other serious physical or mental health condition, or abnormal test results, that researchers feel would make participation unsafe or unsuitable.
- You have or have had a malignant (cancerous) tumour.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 0571-56007429
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Assessing patient nutritional improvement using Third Lumbar Skeletal Muscle Index (L3-SMI).; The improvement of frailty in patients treated by the Frailty Phenotype (FP) Scale assessment.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.