Controlled Trial of 3,4-Diaminopyridine (3-4DAP) in Lambert-Eaton Myasthenic Syndrome (LEMS) (3-4DAP)
Primary Purpose
Muscle Weakness
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
3-4 Diaminopyridine
Sponsored by
About this trial
This is an interventional treatment trial for Muscle Weakness focused on measuring fluctuating muscle weakness, hyporeflexia, autonomic Dysfunction
Eligibility Criteria
Inclusion Criteria: -Male or female majority between 45 and 60 years of age
- diagnosed with Lambert-Eaton Myasthenic Syndrome.
- subjects must be taking full dose of pyridostigmine
Exclusion Criteria: - does subject have a history of liver problems?
- does subject have a history of prolonged QTc syndrome (which is a condition where there is prolongation between the start of the Q wave and the end of the T wave in the heart's electrical cycle).
Sites / Locations
- Dartmouth-Hitchcock Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
3-4 Diaminopyridine (DAP)
Arm Description
Outcomes
Primary Outcome Measures
Number of Participants That Showed Improvement in Muscle Weakness During Their Last Study Related Visit
Muscle weakness will be assessed monthly for the first 3 months based on clinical assessment during office visits. Muscle weakness will then be assessed every 6 months once the patient is stabilized based on clinical assessments during office visits. The assessment of whether there was an improvement in muscle weakness, based on the PI's clinical judgment, was noted during the last study visit completed by the participant.
Secondary Outcome Measures
Full Information
NCT ID
NCT02090725
First Posted
March 14, 2014
Last Updated
May 1, 2019
Sponsor
Jeffrey A. Cohen, MD
Collaborators
Jacobus Pharmaceutical
1. Study Identification
Unique Protocol Identification Number
NCT02090725
Brief Title
Controlled Trial of 3,4-Diaminopyridine (3-4DAP) in Lambert-Eaton Myasthenic Syndrome (LEMS)
Acronym
3-4DAP
Official Title
Controlled Trial of 3,4-Diaminopyridine in LEMS
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Terminated
Why Stopped
Drug receive FDA approval
Study Start Date
February 2004 (undefined)
Primary Completion Date
July 2018 (Actual)
Study Completion Date
November 28, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jeffrey A. Cohen, MD
Collaborators
Jacobus Pharmaceutical
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The main purpose for this study is to provide access to 3,4 DAP, a drug which has demonstrated to be effective in treating weakness associated with Lambert-Eaton Myasthenic Syndrome. LEMS is a rare autoimmune cause of a defect in neuromuscular transmission. The disorder is clinically characterized by fluctuating muscle weakness, hyporeflexia and autonomic dysfunction.
Detailed Description
More than half of LEMS cases are associated with malignancy, usually small cell lung cancer. These paraneoplastic cases progress more quickly than primary autoimmune LEMS. An overlap syndrome with other autoimmune diseases is often detected in LEMS patients.
3,4 DAP is effective in LEMS because it increases calcium influx into the nerve terminal by blocking potassium efflux and thereby prolonging the presynaptic action potential. 3,4 DAP is less likely to provoke epileptic seizures than its precursor, 4-aminopyridine, because it is less able to cross the blood-brain barrier. 3,4 DAP is effective in increasing strength and improving autonomic symptoms in LEMS patients of both the primary autoimmune and paraneoplastic etiologies.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Weakness
Keywords
fluctuating muscle weakness, hyporeflexia, autonomic Dysfunction
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)
8. Arms, Groups, and Interventions
Arm Title
3-4 Diaminopyridine (DAP)
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
3-4 Diaminopyridine
Other Intervention Name(s)
3-4 DAP
Primary Outcome Measure Information:
Title
Number of Participants That Showed Improvement in Muscle Weakness During Their Last Study Related Visit
Description
Muscle weakness will be assessed monthly for the first 3 months based on clinical assessment during office visits. Muscle weakness will then be assessed every 6 months once the patient is stabilized based on clinical assessments during office visits. The assessment of whether there was an improvement in muscle weakness, based on the PI's clinical judgment, was noted during the last study visit completed by the participant.
Time Frame
Participants were followed until they withdrew or the study ended. Time frame ranged from 1 month to 3 years.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: -Male or female majority between 45 and 60 years of age
diagnosed with Lambert-Eaton Myasthenic Syndrome.
subjects must be taking full dose of pyridostigmine
Exclusion Criteria: - does subject have a history of liver problems?
does subject have a history of prolonged QTc syndrome (which is a condition where there is prolongation between the start of the Q wave and the end of the T wave in the heart's electrical cycle).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey A. Cohen, MD
Organizational Affiliation
Dartmouth-Hitchcock Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dartmouth-Hitchcock Medical Center
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03221
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Controlled Trial of 3,4-Diaminopyridine (3-4DAP) in Lambert-Eaton Myasthenic Syndrome (LEMS)
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