Fingolimod compassionate use program. Case study on the concept of a therapy option for multiple sclerosis prior to marketing approval

被引:0
作者
Haas, J. [1 ]
Linker, R. A. [2 ]
Hartung, H. P. [3 ]
Meergans, M. [4 ]
Ortler, S. [4 ]
Tracik, F. [3 ,4 ]
机构
[1] Judisches Krankenhaus, Neurol Klin, D-13347 Berlin, Germany
[2] Univ Klinikum Erlangen, Erlangen, Germany
[3] Univ Dusseldorf, Univ Klinikum, Dusseldorf, Germany
[4] Novartis Pharma GmbH Nurnberg, Nurnberg, Germany
来源
NERVENARZT | 2012年 / 83卷 / 12期
关键词
Multiple sclerosis; Fingolimod hydrochloride; Compassionate use; Effectiveness; Safety profile; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; ORAL FINGOLIMOD; FTY720; NATALIZUMAB; MITOXANTRONE; INTERFERON; LESSONS;
D O I
10.1007/s00115-012-3612-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In order to meet the needs of therapy of multiple sclerosis (MS) new immune therapies with a user-friendly application and better effectiveness together with good tolerability are necessary. With respect to its potential to improve MS therapy, patients with a high medical need were given access to Fingolimod even before marketing approval. Therefore, a compassionate use program unique in the field of MS was initiated. In total 137 centers participated (75 % outpatient neurologists and 25 % hospitals). Within 19 weeks 135 patients were enrolled to receive Fingolimod. The patients in the compassionate use program can be representatively described as showing hardly controllable disease activity and progression with currently available, often poorly tolerated therapy. The compassionate use program for these patients offered better control of the disease with Fingolimod. The adverse events were as expected. The Fingolimod compassionate use program demonstrated the need for this new therapeutic option. Patients who were not yet sufficiently treated were provided with an effective therapy with a good safety profile and a user-friendly administration form.
引用
收藏
页码:1575 / +
页数:6
相关论文
共 28 条
[1]   Neuroprotection, regeneration and immunomodulation: broadening the therapeutic repertoire in multiple sclerosis [J].
Aktas, Orhan ;
Kieseier, Bernd ;
Hartung, Hans-Peter .
TRENDS IN NEUROSCIENCES, 2010, 33 (03) :140-152
[2]   Fingolimod (FTY720): discovery and development of an oral drug to treat multiple sclerosis [J].
Brinkmann, Volker ;
Billich, Andreas ;
Baumruker, Thomas ;
Heining, Peter ;
Schmouder, Robert ;
Francis, Gordon ;
Aradhye, Shreeram ;
Burtin, Pascale .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (11) :883-897
[3]   FTY720 (fingolimod) in Multiple Sclerosis: therapeutic effects in the immune and the central nervous system [J].
Brinkmann, Volker .
BRITISH JOURNAL OF PHARMACOLOGY, 2009, 158 (05) :1173-1182
[4]  
Bundesministerium fur Gesundheit, 2010, VER INV ARZ OHN GEN
[5]   Mechanism of Action of Oral Fingolimod (FTY720) in Multiple Sclerosis [J].
Chun, Jerold ;
Hartung, Hans-Peter .
CLINICAL NEUROPHARMACOLOGY, 2010, 33 (02) :91-101
[6]   Oral Fingolimod or Intramuscular Interferon for Relapsing Multiple Sclerosis [J].
Cohen, Jeffrey A. ;
Barkhof, Frederik ;
Comi, Giancarlo ;
Hartung, Hans-Peter ;
Khatri, Bhupendra O. ;
Montalban, Xavier ;
Pelletier, Jean ;
Capra, Ruggero ;
Gallo, Paolo ;
Izquierdo, Guillermo ;
Tiel-Wilck, Klaus ;
de Vera, Ana ;
Jin, James ;
Stites, Tracy ;
Wu, Stacy ;
Aradhye, Shreeram ;
Kappos, Ludwig .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 362 (05) :402-415
[7]   Brain sphingosine-1-phosphate receptors: Implication for FTY720 in the treatment of multiple sclerosis [J].
Dev, Kumlesh K. ;
Mullershausen, Florian ;
Mattes, Henri ;
Kuhn, Rainer R. ;
Bilbe, Graeme ;
Hoyer, Daniel ;
Mir, Anis .
PHARMACOLOGY & THERAPEUTICS, 2008, 117 (01) :77-93
[8]   Long-Term Persistence With the Immunomodulatory Drugs for Multiple Sclerosis: A Retrospective Database Study [J].
Evans, Charity ;
Tam, Jennifer ;
Kingwell, Elaine ;
Oger, Joel ;
Tremlett, Helen .
CLINICAL THERAPEUTICS, 2012, 34 (02) :341-350
[9]  
Giovannoni G, 2012, MULT SCLER
[10]   New cases of progressive multifocal leukoencephalopathy after treatment with natalizumab [J].
Hartung, Hans-Peter .
LANCET NEUROLOGY, 2009, 8 (01) :28-31