Dalfampridine in Egyptian Patients With Multiple Sclerosis
NCT05730738 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2023-02-16
Summary
The only approved treatment for impaired ambulation in MS is Dalfampridine (also known as fampridine, 4-aminopyridine, 4-AP). Fampridine penetrates the blood-brain barrier and improves impaired axonal conduction by selectively blocking potassium channels. Moreover, further studies investigated the possible beneficial effect of dalfampridine on cognitive functions and fatigue.
The main objective of this study is to investigate the effect of dalfampridine on gait impairment, cognitive functions and fatigue in a sample of Egyptian patients with multiple sclerosis.
Conditions
Interventions
- DRUG
-
Dalfampridine ER, 10 Mg Oral Tablet, Extended Release
The only approved treatment for impaired ambulation in MS is Dalfampridine (also known as fampridine, 4-aminopyridine, 4-AP). Fampridine penetrates the blood-brain barrier and improves impaired axonal conduction by selectively blocking potassium channels
- DRUG
-
placebo similar to Dalfampridine capsule
Sponsors & Collaborators
-
Ain Shams University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-06-01
- Primary Completion
- 2023-12-01
- Completion
- 2024-12-01
Countries
- Egypt
Study Locations
More Related Trials
-
Expanded Access Study Amifampridine Phosphate in Lambert-Eaton Myasthenic Syndrome (LEMS),Congenital Myasthenic Syndrome
NCT02189720 ·Status: APPROVED_FOR_MARKETING
-
Randomized Study of 3,4-Diaminopyridine for Lambert-Eaton Myasthenic Syndrome
NCT00004832 ·Status: COMPLETED ·Phase: NA
-
Dalfampridine and Gait in Spinocerebellar Ataxias
NCT01811706 ·Status: COMPLETED ·Phase: NA
-
Safety and Tolerability of Dalfampridine in Subjects With Cerebral Palsy
NCT01468350 ·Status: COMPLETED ·Phase: PHASE1
-
An Open Label, Proof of Concept Study to Evaluate the Effects of Dalfampridine Withdrawal on Gait and Balance Parameters in Subjects With Multiple Sclerosis (MS)
NCT01535664 ·Status: COMPLETED
-
Effectiveness of 3,4-Diaminopyridine in Lambert-Eaton Myasthenic Syndrome
NCT01511978 ·Status: COMPLETED ·Phase: PHASE2
-
Study of NMDA Antagonists and Neuropathic Pain
NCT01602185 ·Status: COMPLETED ·Phase: PHASE2
-
Phase 3 Study of Dexpramipexole in ALS
NCT01281189 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Evaluate the Long-Term Safety, Tolerability and Efficacy of Dalfampridine.
NCT02422940 ·Status: TERMINATED ·Phase: PHASE3
-
Effect of Dalfampridine in Patients With Hereditary Spastic Paraplegia
NCT05613114 ·Status: COMPLETED ·Phase: NA
-
Dexamfetamine Sulphate in Patients With Glioma Suffering From Severe Asthenia
NCT02363075 ·Status: UNKNOWN ·Phase: PHASE3
-
Prolonged-release Fampridine as Adjunct Therapy to Active Motor Training in MS Patients
NCT02146534 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Assess the Safety, Tolerability, and Pharmacology of Darifenacin in Patients With ALS
NCT06249867 ·Status: RECRUITING ·Phase: PHASE2
-
Controlled Trial to Evaluate Amifampridine Phosphate in Spinal Muscular Atrophy Type 3 Patients
NCT03781479 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Assess FLX-787 in Subjects With Motor Neuron Disease Experiencing Muscle Cramps.
NCT03196375 ·Status: TERMINATED ·Phase: PHASE2
-
Effect of Dalfampridine (4-AP) on Genioglossus Muscle Activity in Healthy Adults
NCT02656160 ·Status: COMPLETED ·Phase: PHASE2
-
Use Of 3,4-Diaminopyridine (3,4-DAP) In The Treatment Of Lambert Eaton Myasthenic Syndrome
NCT01373333 ·Status: NO_LONGER_AVAILABLE
-
Investigating NMJ Defects in SMA Following Central and Peripheral SMN Restoration
NCT05219487 ·Status: COMPLETED
-
3,4-Diaminopyridine Use in Lambert-Eaton Myasthenic Syndrome(LEMS) and Congenital Myasthenic Syndromes (CMS)
NCT00872950 ·Status: APPROVED_FOR_MARKETING
-
Treatment of Lambert-Eaton Syndrome With 3,4 DAP
NCT00704925 ·Status: NO_LONGER_AVAILABLE
-
Study to Evaluate Multiple Ascending Dose and Multi-Dose of DT-216 in Adult Patients With Friedreich Ataxia
NCT05573698 ·Status: COMPLETED ·Phase: PHASE1
-
Long Term Safety of Amifampridine Phosphate in Spinal Muscular Atrophy 3
NCT03819660 ·Status: TERMINATED ·Phase: PHASE2
-
Controlled Trial of 3,4-Diaminopyridine (3-4DAP) in Lambert-Eaton Myasthenic Syndrome (LEMS)
NCT02090725 ·Status: TERMINATED ·Phase: PHASE2
-
Safety and Efficacy of Oral Fampridine-Sustained Release (SR) for the Treatment of Spasticity Resulting From Spinal Cord Injury
NCT01683838 ·Status: COMPLETED ·Phase: PHASE3
-
A Study Investigating the Safety and Tolerability of Deferiprone in Patients With Friedreich's Ataxia
NCT00530127 ·Status: COMPLETED ·Phase: PHASE1/PHASE2