Motor Neuron Disease Clinical Trial
Official title:
A Fase II, Randomized, Double-Blind, Placebo-Controlled, Multicentre Study for the Safety and Efficacy on Spasticity Symptoms of a Cannabis Sativa Extract in Motor Neuron Disease Patients
The clinical primary hypothesis is that there will be a difference between a Cannabis Sativa
extract and placebo in their effect on spasticity in Motor Neuron Disease (MND) patients
with signs of involvement of the upper motor neuron (UMN) resulting in disabling spasticity.
Secondary goals of the study are to evidence of improvement in other symptoms (in particular
pain), and to show favourable trends on functionality measures. Finally, cannabis based drug
safety and tolerability will be studied through vital parameters (including weight and
pulmonary function) measurement, and analyzing ALS function rating scale progression slope
hopefully, showing a slowing of the functional values decrease, owing to cannabis
neuroprotective effects)
CANALS project has as a main objective to analyse the safety profile, tolerability and
efficacy of a Cannabis Sativa (Sativex) derivative on patients affected by spasticity due to
motor neuron disease.
Muscular rigidity (or spasticity) is a symptom that affects many patients with motor neuron
disease, concurring to reduce personal autonomy, patients' quality of life and can
potentially cause secondary symptomatology (as pain or secondary muscular retractions).
Currently available anti-spasticity drugs are often unsatisfactory and their pharmacological
action can cause weakness as a secondary effect. There many arguments supporting the use of
cannabinoid derivatives in motor neuron diseases. Cannabinoids receptor is expresses both in
the brain and in the spinal cord. In animal models cannabinoids have an anti-spasticity
effect. Moreover recent studies on ALS animal models demonstrated a neuroprotective effect
of cannabinoids, including the preservation of the motor ability and a survival increase of
the treated animals. Recently many clinical trials (some of them performed at the
Neurological Division of San Raffaele Hospital) demonstrated cannabinoid efficacy on
spasticity in Multiple Sclerosis patients. CAnnabinois would be able to reduce spasticity
with no secondary weakness effect on treated patients. The results of these studies led to
the drug approval in certain countries and by the European Community for the treatment of
spasticity in Multiple Sclerosis.
The aim of this study is to analyze the safety, tolerability and efficacy profile of a
Cannabis Sativa (Sativex) derivative on patients affected by spasticity due to motor neuron
disease ( Amyotrophic Lateral Sclerosis and Primary Lateral Sclerosis). The study will be
performed along 7 weeks. During the first week will be asked patients to note down in the
clinical diary elements related to their symptomatology. Afterwards patients will be
randomized in two groups: drug-treated and placebo treated. The study will be followed by a
6-weeks open-label phase during which all patients will receive the active drug (Phase B)
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT04579666 -
MERIDIAN: A Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Adults With Amyotrophic Lateral Sclerosis (ALS)
|
Phase 2 | |
Completed |
NCT03706391 -
Study of ALS Reversals 4: LifeTime Exposures
|
||
Active, not recruiting |
NCT03067857 -
Autologous Bone Marrow-Derived Stem Cell Therapy for Motor Neuron Disease
|
Phase 1/Phase 2 | |
Completed |
NCT02464748 -
Telehealth in Motor Neurone Disease
|
N/A | |
Completed |
NCT00956488 -
Supported Treadmill Ambulation Training (STAT) for Patients Diagnosed With Amyotrophic Lateral Aclerosis
|
Phase 1/Phase 2 | |
Terminated |
NCT00537446 -
Effect of Noninvasive Ventilation on Lung Function in Amyotrophic Lateral Sclerosis
|
N/A | |
Recruiting |
NCT04944940 -
Clinical, Molecular and Imaging Biomarkers in Spinal and Bulbar Muscular Atrophy (SBMA)
|
||
Recruiting |
NCT03362658 -
Novel MRI Biomarkers for Monitoring Disease Progression in ALS
|
||
Completed |
NCT00714636 -
Cerebrospinal Fluid Repository
|
N/A | |
Completed |
NCT00076687 -
Safety Study of Botulinum Toxin Type A in Post-Upper Limb Stroke Patients With Reduced Lung Function
|
Phase 2 | |
Completed |
NCT00071435 -
Brain Function in Primary Lateral Sclerosis
|
N/A | |
Completed |
NCT00001220 -
Ultrasound and Videofluoroscopy for Diagnosing Swallowing Disorders
|
N/A | |
Completed |
NCT03487263 -
Dose-Escalation, Safety and Pharmacokinetic Study of IC14 in Motor Neurone Disease
|
Phase 1 | |
Enrolling by invitation |
NCT05725759 -
Rehabilitation in SOD1 ALS Treated With Tofersen
|
||
Active, not recruiting |
NCT03811301 -
[BrainConnexion] - Neurodevice Phase I Trial
|
N/A | |
Completed |
NCT02469896 -
A Trial of Tocilizumab in ALS Subjects
|
Phase 2 | |
Completed |
NCT02011204 -
Study of Electrical Impedance Myography (EIM) in ALS
|
N/A | |
Completed |
NCT01495390 -
A Longitudinal Study of Amyotrophic Lateral Sclerosis (ALS) Biomarkers
|
N/A | |
Completed |
NCT02870634 -
Phase 1 Dose Escalation and PK Study of Cu(II)ATSM in ALS/MND
|
Phase 1 | |
Recruiting |
NCT06201650 -
Neurofilament Light Chain in Amyotrophic Lateral Sclerosis
|