Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:51 PM
Ignite Modification Date:
2025-12-24 @ 10:51 PM
NCT ID:
NCT03293069
Eligibility Criteria:
Inclusion Criteria:
* Categorized as; possible, laboratory supported probable, probable, or definite ALS (revised El Escorial criteria)
* Spinal and bulbar forms of ALS
* Duration of the disease of less than 18 months since the first symptoms of motor deficit or amyotrophy (isolated cramps or fasciculation will not be considered).
* Duration of the disease of less than 6 months since the diagnosis
* An upright slow vital capacity ≥ 75% of the predicted value for age, height, and sex or at least one test on inspiratory pressure ≥ 60% of the predicted value for age, height, and sex which could be either maximal inspiratory pressure or a SNIFF test. (The best predictive test is sniff test but sometime patients are not able to do it.) (In case of a limit abnormal value for one of them, it will be recommended that patient re-assessment occurs three months later).
* A mild functional handicap score for ALSFRS-R ≥36
* An upright slow vital capacity \> 70% of the predicted value for age, height, and sex and
* Able to swallow (required for oral treatment)
* Patients weight included between 40 kg and 130 kg
* If the patient is under riluzole, it has to be for at least 1 month before inclusion with stable dose (to rule out the principal risk of hepatitis)
Exclusion Criteria:
* Patients with high frequency of comorbidity or vital risks that may reasonably impair life expectancy
* Progressing axis I psychiatric disorders (psychosis, hallucinations, substance addiction, bipolar disorder, severe depression, suicidal ideation), in accordance with the Diagnostic and Statistical Manual of Mental Disorders. Before entry into the study, exclusion or stabilization of conditions must occur for patients suffering from mild or moderate depressive episodes (not in remission) or severe and uncontrolled anxiety.
* Dementia according to the Diagnostic and Statistical Manual of Mental Disorders
* Exposure to any other experimental drug up to 30 days before day 1
* Due to the risk of agranulocytosis (estimated at 2%) caused by the Investigational Medicinal Products (IMPs) and the unknown mechanism by which this agranulocytosis is induced, combining Deferiprone with other medicinal products known to cause agranulocytosis (as described in the IB) will not be allowed. Such medicinal products include clozapine as well as some NSAIDs (e.g. Phenylbutazone or Metamizole), antithyroid agents, sulfonamide antibiotics or methotrexate.
* A history of relapsing neutropenia
* Patients with agranulocytosis or with a history of agranulocytosis.
* Hypersensitivity to Deferiprone
* Patients with anaemia (regardless of latter aetiology) or a history of another haematological disease. Haemochromatosis is not an exclusion criterion if controlled.
* Pregnant or breastfeeding women or women of childbearing potential not taking highly effective contraception.
* Kidney or liver failure.
* Inability to provide informed consent.
* Participation in another clinical trial within 1 month prior to inclusion in the study
* Patients under trusteeship
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT03293069
Study Brief:
Protocol Section:
NCT03293069