Delayed-Release Dimethyl Fumarate and Pregnancy: Preclinical Studies and Pregnancy Outcomes from Clinical Trials and Postmarketing Experience
Status PubMed-not-MEDLINE Jazyk angličtina Země Nový Zéland Médium print-electronic
Typ dokumentu časopisecké články
PubMed
26662361
PubMed Central
PMC4685863
DOI
10.1007/s40120-015-0033-1
PII: 10.1007/s40120-015-0033-1
Knihovny.cz E-zdroje
- Klíčová slova
- Clinical trial, Delayed-release dimethyl fumarate, Multiple sclerosis, Postmarketing, Preclinical, Pregnancy, Safety, Women,
- Publikační typ
- časopisecké články MeSH
INTRODUCTION: Delayed-release dimethyl fumarate (DMF; also known as gastro-resistant DMF) is an oral agent for the treatment of relapsing forms of multiple sclerosis (MS). No formal studies of DMF were conducted in pregnant women, although pregnancies have occurred during clinical trials and in the postmarketing setting. METHODS: Preclinical developmental and reproductive toxicology studies were performed with DMF in rats and rabbits. As of March 26, 2014, the DMF clinical development program included a total of 4132 subjects consisting of 2898 patients with MS, 320 psoriasis patients, 101 rheumatoid arthritis patients, and 813 healthy volunteers. Subjects were required to use reliable contraception and immediately discontinue treatment in the event of pregnancy. RESULTS: Animal studies showed no evidence of impaired fertility or teratogenicity with DMF. Overall as of June 30, 2014, 63 pregnancies were reported in clinical trials. Outcomes are known for 39 of 42 subjects receiving DMF and include 26 live births (67%), three spontaneous abortions (8%), and 10 elective terminations (26%); follow-up is ongoing in 2 cases and one patient was lost to follow-up. The incidence of spontaneous abortion in subjects exposed to DMF was consistent with the expected rate of early pregnancy loss in the general population (12-22%). A total of 135 pregnancies were reported in the postmarketing setting (spontaneous and solicited reports). Outcomes are known for 30 cases and include 10 live births, 13 spontaneous abortions, and 5 elective terminations; follow-up is ongoing in 103 cases and 2 patients have been lost to follow-up. CONCLUSION: Although data are limited and all known exposures have occurred in the first trimester, no increased risk of fetal abnormalities or adverse pregnancy outcomes associated with gestational exposure to DMF has been observed. FUNDING: Biogen, Inc.
Alnylam Pharmaceuticals Inc Cambridge MA USA
Charles University Prague Czech Republic
Mellen Center for Multiple Sclerosis Treatment and Research Cleveland Clinic Cleveland OH USA
Montreal Neurological Institute and Hospital McGill University Montreal QC Canada
Multiple Sclerosis Program Baylor Institute for Immunology Research Dallas TX USA
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Tullman MJ. Overview of the epidemiology, diagnosis, and disease progression associated with multiple sclerosis. Am J Manag Care. 2013;19:S15–S20. PubMed
Lu E, Wang BW, Synnes A, Dahlgren L, Sadovnick AD, Tremlett H. A review of safety-related pregnancy data surrounding the oral disease-modifying drugs for multiple sclerosis. CNS Drugs. 2014;28:89–94. doi: 10.1007/s40263-013-0131-5. PubMed DOI
Lu E, Wang BW, Guimond C, et al. Safety of disease-modifying drugs for multiple sclerosis in pregnancy: current challenges and future considerations for effective pharmacovigilance. Expert Rev Neurother. 2013;13(3):251–261. doi: 10.1586/ern.13.12. PubMed DOI
Coyle PK, Christie S, Fodor P, et al. Multiple sclerosis gender issues: clinical practices of women neurologists. Mult Scler. 2004;10:582–588. doi: 10.1191/1352458504ms1083oa. PubMed DOI
Langer-Gould AM. The pill times 2: what every woman with multiple sclerosis should know. Neurology. 2014;82:1–2. doi: 10.1212/WNL.0000000000000155. PubMed DOI
Fragoso YD, Boggild M, Macias-Islas MA, et al. The effects of long-term exposure to disease-modifying drugs during pregnancy in multiple sclerosis. Clin Neurol Neurosurg. 2013;115:154–159. doi: 10.1016/j.clineuro.2012.04.024. PubMed DOI
Tecfidera (dimethyl fumarate) prescribing information. Cambridge: Biogen Inc.; 2013. http://www.tecfidera.com/pdfs/full-prescribing-information.pdf. Accessed Oct 21, 2014.
Linker RA, Lee DH, Ryan S, et al. Fumaric acid esters exert neuroprotective effects in neuroinflammation via activation of the Nrf2 antioxidant pathway. Brain. 2011;134:678–692. doi: 10.1093/brain/awq386. PubMed DOI
Scannevin RH, Chollate S, Jung MY, et al. Fumarates promote cytoprotection of central nervous system cells against oxidative stress via the nuclear factor (erythroid-derived 2)-like 2 pathway. J Pharmacol Exp Ther. 2012;341:274–284. doi: 10.1124/jpet.111.190132. PubMed DOI
Gold R, Kappos L, Arnold DL, et al. Placebo-controlled phase 3 study of oral BG-12 for relapsing multiple sclerosis. N Engl J Med. 2012;367(12):1098–1107. doi: 10.1056/NEJMoa1114287. PubMed DOI
Fox RJ, Miller DH, Phillips T, et al. Placebo-controlled phase 3 study of oral BG-12 or glatiramer in multiple sclerosis. N Engl J Med. 2012;367(12):1087–1097. doi: 10.1056/NEJMoa1206328. PubMed DOI
International Conference on Harmonisation [ICH] S5(R2) guideline: Detection of Toxicity to Reproduction for Medicinal Products & Toxicity to Male Fertility, current Step 4 version. 2005.
Chahoud I, Buschmann J, Clark R, et al. Classification terms in developmental toxicology: need for harmonization. Report of the second workshop on the terminology in developmental toxicology. Reprod Toxicol. 1999;13(1):77–82. doi: 10.1016/S0890-6238(98)00060-4. PubMed DOI
Chahoud I, Paumgartten FJR. Relationships between fetal body weight of Wistar rats at term and the extent of skeletal ossification. Braz J Med Biol Res. 2005;38:565–575. doi: 10.1590/S0100-879X2005000400010. PubMed DOI
Carney EW, Kimmel CA. Interpretation of skeletal variations for human risk assessment: delayed ossification and wavy ribs. Birth Defects Res B Dev Reprod Toxicol. 2007;80(6):473–496. doi: 10.1002/bdrb.20133. PubMed DOI
Matsuzawa T, Nakata M, Goto I, Tsushima M. Dietary deprivation induces fetal loss and abortion in rabbits. Toxicology. 1981;22(3):255–259. doi: 10.1016/0300-483X(81)90088-3. PubMed DOI
Clark RL, Antonello JM, Wenger JD, Deverle-Brooks K, Duchai DM. Selection of food allotment for New Zealand white rabbits in developmental toxicity studies. Fundam Appl Toxicol. 1991;17(3):584–592. doi: 10.1016/0272-0590(91)90208-L. PubMed DOI
Matsuoka T, Mizoguchi Y, Serizawa K, Ishikura T, Mizuguchi H, Asano Y. Effects of stage and degree of restricted feeding on pregnancy outcome in rabbits. J Toxicol Sci. 2006;31(2):169–175. doi: 10.2131/jts.31.169. PubMed DOI
Cappon GD, Fleeman TL, Chapin RE, Hurtt ME. Effects of feed restriction during organogenesis on embryo-fetal development in rabbit. BDR(B). 2006;74:424–30. PubMed
Prentice DE, Meikle AW. A review of drug-induced Leydig cell hyperplasia and neoplasia in the rat and some comparisons with man. Hum Exp Toxicol. 1995;14(7):562–572. doi: 10.1177/096032719501400703. PubMed DOI
Cook JC, Klinefelter GR, Hardisty JF, Sharpe RM, Foster PM. Rodent Leydig cell tumorigenesis: a review of the physiology, pathology, mechanisms, and relevance to humans. Crit Rev Toxicol. 1999;29(2):169–261. doi: 10.1080/10408449991349203. PubMed DOI
Clegg ED, Cook JC, Chapin RE, Foster PM, Daston GP. Leydig cell hyperplasia and adenoma formation: mechanisms and relevance to humans. Reprod Toxicol. 1997;11(1):107–121. doi: 10.1016/S0890-6238(96)00203-1. PubMed DOI
Zaw W, Stone DG. Caudal regression syndrome in twin pregnancy with type II diabetes. J Perinatol. 2002;22(2):171–174. doi: 10.1038/sj.jp.7210614. PubMed DOI
Litjens NH, van Strijen E, van Gulpen C, et al. In vitro pharmacokinetics of anti-psoriatic fumaric acid esters. BMC Pharmacol. 2004;4:22. doi: 10.1186/1471-2210-4-22. PubMed DOI PMC
García-Enguídanos A, Calle ME, Valero J, Luna S, Domínguez-Rojas V. Risk factors in miscarriage: a review. Eur J Obstet Gynecol Reprod Biol. 2002;102(2):111–119. doi: 10.1016/S0301-2115(01)00613-3. PubMed DOI
Gilenya (fingolimod) prescribing information. East Hanover: Novartis International AG; 2014. http://www.pharma.us.novartis.com/product/pi/pdf/gilenya.pdf. Accessed Oct 21, 2014.
Aubagio (teriflunomide) prescribing information. Cambridge: Genzyme Corporation, a Sanofi company; 2012. http://products.sanofi.us/aubagio/aubagio.pdf. Accessed Oct 21, 2014.
Karlsson G, Francis G, Koren G, et al. Pregnancy outcomes in the clinical development program of fingolimod in multiple sclerosis. Neurology. 2014;82:674–680. doi: 10.1212/WNL.0000000000000137. PubMed DOI PMC
Weber-Schoendorfer C, Schaefer C. Multiple sclerosis, immunomodulators, and pregnancy outcome: a prospective observational study. Mult Scler. 2009;15:1037–1042. doi: 10.1177/1352458509106543. PubMed DOI
Amato MP, Portaccio E, Ghezzi A, et al. Pregnancy and fetal outcomes after interferon-β exposure in multiple sclerosis. Neurology. 2010;75:1794–1802. doi: 10.1212/WNL.0b013e3181fd62bb. PubMed DOI
Houtchens MK, Kolb CM. Multiple sclerosis and pregnancy: therapeutic considerations. J Neurol. 2013;260:1202–1214. doi: 10.1007/s00415-012-6653-9. PubMed DOI
Dahl J, Myhr KM, Daltveit AK, Gilhus NE. Pregnancy, delivery and birth outcome in different stages of maternal multiple sclerosis. J Neurol. 2008;255(6):623–627. doi: 10.1007/s00415-008-0757-2. PubMed DOI
Lu E, Wang BW, Guimond C, Synnes A, Sadovnick D, Tremlett H. Disease-modifying drugs for multiple sclerosis in pregnancy: a systematic review. Neurology. 2012;79(11):1130–1135. doi: 10.1212/WNL.0b013e3182698c64. PubMed DOI PMC