Motor Neurone Disease Trial, Recruiting NCT06765499 Sponsor: First People's Hospital of Hangzhou Condition: Motor Neurone Disease
Back to Motor Neurone Disease

Motor Neurone Disease Trial, Recruiting

NCT06765499
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
First People's Hospital of Hangzhou
Registry
ClinicalTrials.gov
Start date
4 March 2025
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov