Compassionate Use of 3,4-Diaminopyridine
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Purpose
This is a continuing project to provide 3,4 diaminopyridine (DAP) under a treatment-use (IND) Investigational New Drug to patients with Lambert-Eaton myasthenic syndrome (LEMS) or congenital myasthenia gravis (CMG).
| Condition | Intervention |
|---|---|
|
Lambert Eaton Myasthenic Syndrome (LEMS) Myasthenic Syndromes, Congenital |
Drug: 3,4-diaminopyridine |
| Study Type: | Expanded Access What is Expanded Access? |
| Official Title: | Compassionate Use of 3,4-Diaminopyridine in Lambert-Eaton Myasthenic Syndrome and Congenital Myasthenia Gravis |
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Drug: 3,4-diaminopyridine
The diagnosis of LEMS or CMG will have been made based on clinical and electromyographic findings, and all patients will have been referred to the PI for DAP treatment. This study will enroll minors and adults.
CMG patients under age 18 will be included if their parent or guardian gives written permission. Minors who turn 18 while on the study will be re-consented as adults.
The dose of DAP will be determined individually for each patient. Adults will start with a dose of 10 mg 3 or 4 times a day, increasing over several weeks to the dose that produces the maximum symptomatic response, not to exceed 100 mg/day. Mestinon will then be added at low doses, increasing to the dose that produces the best response, not to exceed 360 mg/day. In children, equivalent doses of these medications will be given calculated on a surface area basis. The doses of DAP and Mestinon will be periodically adjusted to assure that the smallest effective doses are used.
Patients who achieve significant clinical benefit from DAP, as judged by the study PI and the patient, may continue taking DAP as long as the drug is available from the sponsor, and as long as they return for regular follow-up at the Duke MG Clinic. Patients who are unable to return for regular follow-up will be required to have their local physician obtain DAP for them from the sponsor.
Eligibility| Genders Eligible for Study: | Both |
Inclusion Criteria:
- diagnosis of either Lambert Eaton myasthenic syndrome (LEMS) or congenital myasthenic gravis (CMG)
- women of childbearing potential must have negative pregnancy test and agree to practice adequate contraception while taking DAP
- must be competent to give consent
Exclusion Criteria:
- known seizure disorder
- pregnancy
- known cardiac arrhythmia or evidence of these on screening ECG
- known hepatic, renal or hematologic disease
Contacts and Locations| Contact: Vern C. Juel, M.D. | 919-684-4044 | vern.juel@duke.edu |
| United States, North Carolina | |
| Duke University Hospital | |
| Durham, North Carolina, United States, 27710 | |
| Contact: Vern C. Juel, M.D. 919-684-4044 vern.juel@duke.edu | |
| Principal Investigator: Vern C. Juel, M.D. | |
| Principal Investigator: | Vern C. Juel, M.D. | Duke University School of Medicine |
More Information
No publications provided
| Responsible Party: | Vern C. Juel, M.D., Associate Professor of Medicine, Duke University Medical Center |
| ClinicalTrials.gov Identifier: | NCT01765140 History of Changes |
| Other Study ID Numbers: | Pro00007811 |
| Study First Received: | January 6, 2013 |
| Last Updated: | January 8, 2013 |
| Health Authority: | United States: Food and Drug Administration United States: Institutional Review Board |
Keywords provided by Duke University:
|
3,4 diaminopyridine (DAP) |
Additional relevant MeSH terms:
|
Lambert-Eaton Myasthenic Syndrome Myasthenic Syndromes, Congenital Paraneoplastic Syndromes, Nervous System Nervous System Neoplasms Neoplasms by Site Neoplasms Paraneoplastic Syndromes Autoimmune Diseases of the Nervous System Nervous System Diseases Neurodegenerative Diseases Neuromuscular Junction Diseases Neuromuscular Diseases |
Autoimmune Diseases Immune System Diseases Genetic Diseases, Inborn 3,4-diaminopyridine 4-Aminopyridine Potassium Channel Blockers Membrane Transport Modulators Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Cardiovascular Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on June 18, 2013