Long-term safety and efficacy of eculizumab in generalized myasthenia gravis.
dc.contributor.author | Muppidi, Srikanth | |
dc.contributor.author | Utsugisawa, Kimiaki | |
dc.contributor.author | Benatar, Michael | |
dc.contributor.author | Murai, Hiroyuki | |
dc.contributor.author | Barohn, Richard J | |
dc.contributor.author | Illa, Isabel | |
dc.contributor.author | Jacob, Saiju | |
dc.contributor.author | Vissing, John | |
dc.contributor.author | Burns, Ted M | |
dc.contributor.author | Kissel, John T | |
dc.contributor.author | Nowak, Richard J | |
dc.contributor.author | Andersen, Henning | |
dc.contributor.author | Casasnovas, Carlos | |
dc.contributor.author | de Bleecker, Jan L | |
dc.contributor.author | Vu, Tuan H | |
dc.contributor.author | Mantegazza, Renato | |
dc.contributor.author | O'Brien, Fanny L | |
dc.contributor.author | Wang, Jing Jing | |
dc.contributor.author | Fujita, Kenji P | |
dc.contributor.author | Howard, James F | |
dc.contributor.author | Regain Study Group | |
dc.date.accessioned | 2023-07-19T20:51:36Z | |
dc.date.available | 2023-07-19T20:51:36Z | |
dc.date.issued | 2019-07 | |
dc.date.updated | 2023-07-19T20:51:35Z | |
dc.description.abstract | IntroductionEculizumab is effective and well tolerated in patients with antiacetylcholine receptor antibody-positive refractory generalized myasthenia gravis (gMG; REGAIN; NCT01997229). We report an interim analysis of an open-label extension of REGAIN, evaluating eculizumab's long-term safety and efficacy.MethodsEculizumab (1,200 mg every 2 weeks for 22.7 months [median]) was administered to 117 patients.ResultsThe safety profile of eculizumab was consistent with REGAIN; no cases of meningococcal infection were reported during the interim analysis period. Myasthenia gravis exacerbation rate was reduced by 75% from the year before REGAIN (P < 0.0001). Improvements with eculizumab in activities of daily living, muscle strength, functional ability, and quality of life in REGAIN were maintained through 3 years; 56% of patients achieved minimal manifestations or pharmacological remission. Patients who had received placebo during REGAIN experienced rapid and sustained improvements during open-label eculizumab (P < 0.0001).DiscussionThese findings provide evidence for the long-term safety and sustained efficacy of eculizumab for refractory gMG. Muscle Nerve 2019. | |
dc.identifier.issn | 0148-639X | |
dc.identifier.issn | 1097-4598 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Wiley | |
dc.relation.ispartof | Muscle & nerve | |
dc.relation.isversionof | 10.1002/mus.26447 | |
dc.subject | Regain Study Group | |
dc.subject | Humans | |
dc.subject | Meningococcal Infections | |
dc.subject | Aspergillosis | |
dc.subject | Myasthenia Gravis | |
dc.subject | Heart Diseases | |
dc.subject | Disease Progression | |
dc.subject | Meningococcal Vaccines | |
dc.subject | Treatment Outcome | |
dc.subject | Activities of Daily Living | |
dc.subject | Longitudinal Studies | |
dc.subject | Quality of Life | |
dc.subject | Adult | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Complement Inactivating Agents | |
dc.subject | Muscle Strength | |
dc.subject | Angioedema | |
dc.subject | Antibodies, Monoclonal, Humanized | |
dc.subject | Injection Site Reaction | |
dc.title | Long-term safety and efficacy of eculizumab in generalized myasthenia gravis. | |
dc.type | Journal article | |
pubs.begin-page | 14 | |
pubs.end-page | 24 | |
pubs.issue | 1 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Neurology | |
pubs.organisational-group | Neurology, Neuromuscular Disease | |
pubs.publication-status | Published | |
pubs.volume | 60 |
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