Status:
COMPLETED
A Study of Monepantel in Individuals With Motor Neurone Disease
Lead Sponsor:
Neurizon Therapeutics Limited
Collaborating Sponsors:
FightMND
Calvary Health Care Bethlehem
Conditions:
Motor Neuron Disease
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
Brief Summary
Amyotrophic lateral sclerosis/ Motor Neurone Disease (ALS/MND) is a rare and invariably fatal neurological disease. ALS/MND has a terribly high burden on patients, family and carers, and carries great...
Eligibility Criteria
Inclusion
- Signed informed consent obtained prior to initiation of any study-specific procedures and treatment
- Familial or sporadic ALS/MND diagnosed as clinically possible, probable, or definite according to Awaji-shima Consensus Recommendations
- Seated slow vital capacity (SVC) ≥ 3L in males and ≥ 2.5L in females at screening
- Not taking riluzole or on a stable dose of riluzole for at least 4 weeks prior to the screening visit. While on study, subjects are not allowed to start taking riluzole during the study
- Patient has a competent caregiver who can support the patient's involvement in the study, including assisting the administration of study drug
- Adequate bone marrow reserve, renal and liver function:
- absolute neutrophil count (ANC) ≥1500/µL;
- platelet count ≥ 100,000/µL;
- hemoglobin ≥ 9 g/dL;
- creatinine clearance ≥ 60 mL/min (Cockroft \& Gault formula);
- alanine aminotransferase ALT, SGPT) and/or aspartate aminotransferase (AST, SGOT)
- ≤ 2 x upper limit of normal (ULN);
- total bilirubin ≤ 1.5 x ULN;
- serum albumin ≥ 2.8 g/dL
- Women and men with partners of childbearing potential must use effective contraception while on study treatment and women of childbearing potential must have a negative pregnancy test at screening
Exclusion
- Inability to swallow oral medications or presence of a gastrointestinal disorder (e.g., malabsorption) deemed to jeopardize intestinal absorption of study drug
- Dependence on mechanical ventilation (invasive or non-invasive, including Continuous Positive Airway Pressure (CPAP) or Bi-level Positive Airway Pressure (BiPAP) for any part of day or night prior to the screening visit. Dependence on mechanical ventilation is defined as being unable to lie flat (supine) without it, unable to sleep without it, or daytime use
- Exposure to any other investigational agent within 3 months prior to the screening visit
- Active gastrointestinal disease within 30 days of the screening visit. Gastro-esophageal reflux disease (GERD) is not considered active gastrointestinal disease and is not exclusionary
- Known immune compromising illness or treatment
- Presence of any of the following clinical conditions:
- drug abuse or alcoholism;
- unstable cardiac, pulmonary, renal, hepatic, endocrine, or hematologic disease;
- active infectious disease;
- AIDS or AIDS-related complex;
- diagnosis of malignancy within 2 years of screening (adequately treated basal cell or squamous cell carcinoma of skin or non-invasive bladder cancer or carcinoma in situ of the bladder, breast or cervix are allowed;
- unstable psychiatric illness defined as psychosis or untreated major depression within 90 days of the screening visit;
- neuromuscular disease other than ALS/MND
- Dementia that may affect either outcome measures or patient understanding and/or compliance with study requirements and procedures
- Women and men of childbearing potential not using effective contraception while on study treatment
- Women who are breast-feeding
- Patients at risk of or known to carry a SOD1 mutation or VCP mutation
Key Trial Info
Start Date :
June 28 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 29 2023
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT04894240
Start Date
June 28 2022
End Date
November 29 2023
Last Update
December 21 2023
Active Locations (2)
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1
Macquarie University
Sydney, New South Wales, Australia, 2109
2
Calvary Health Care Bethlehem
Melbourne, Victoria, Australia, 3195