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Chemistry版 - 有了解昨天 FDA批准的bg-12的进来解释一下 (转载)
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相关话题的讨论汇总
话题: fda话题: drug话题: confirm话题: ms话题: fumarate
进入Chemistry版参与讨论
1 (共1页)
n*******n
发帖数: 540
1
【 以下文字转载自 Biology 讨论区 】
发信人: nnnnnnnnn (hv), 信区: Biology
标 题: 有了解昨天 FDA批准的bg-12的进来解释一下
发信站: BBS 未名空间站 (Thu Mar 28 15:11:54 2013, 美东)
富马酸二甲酯,
这么简单的药物,当初怎么发现的?
专利没有问题吗
J**e
发帖数: 15008
2
难怪今天股票暴涨

【在 n*******n 的大作中提到】
: 【 以下文字转载自 Biology 讨论区 】
: 发信人: nnnnnnnnn (hv), 信区: Biology
: 标 题: 有了解昨天 FDA批准的bg-12的进来解释一下
: 发信站: BBS 未名空间站 (Thu Mar 28 15:11:54 2013, 美东)
: 富马酸二甲酯,
: 这么简单的药物,当初怎么发现的?
: 专利没有问题吗

n*******n
发帖数: 540
3
biogen idec 的吗?
p****u
发帖数: 239
4
http://www.medpagetoday.com/Neurology/MultipleSclerosis/38122?i
Dimethyl fumarate has won FDA approval to treat relapsing-remitting forms of
multiple sclerosis and will be sold under the name Tecfidera, the agency
said Wednesday.
Manufactured by Biogen Idec, the drug is also known as BG-12. It becomes the
third oral disease-modifying medication available to treat MS. Others
include fingolimod (Gilenya) and teriflunomide (Aubagio).
Dimethyl fumarate has a novel mechanism of action relative to existing MS
drugs. It is believed to activate the nuclear factor-like 2 transcriptional
pathway, thereby reducing oxidative stress that contributes strongly to
demyelination.
The drug has also been used for many years in Europe and elsewhere to treat
psoriasis, and has also been used as a fungicide and desiccant in furniture
manufacture.
Two placebo-controlled phase III trials served as the basis for approval,
the agency said. Called DEFINE and CONFIRM, they enrolled a total of some 2,
700 patients. In addition to comparing the drug with placebo, CONFIRM
included a third arm with open-label glatiramer acetate (Copaxone), a
standard injectable MS drug.
Both trials demonstrated that dimethyl fumarate was superior to placebo in
preventing relapses and delaying disability progression. It also appeared to
be somewhat more effective than glatiramer acetate in CONFIRM.
The most common adverse effects were gastrointestinal complaints and
flushing. The FDA also noted that the drug carries a risk of lymphocytopenia
, although infections did not appear to be increased as a result in the
phase III studies.
"No drug provides a cure for multiple sclerosis so it is important to have a
variety of treatment options available for patients," said Russell Katz, MD
, director of the Division of Neurology Products in the FDA's Center for
Drug Evaluation and Research, in a statement announcing the approval.
A Biogen competitor, Teva Pharmaceuticals, had petitioned the FDA to hold an
advisory committee meeting on the drug before approving it, citing the
hematologic effects and other risks, but the agency declined to do so.
y*****s
发帖数: 1047
y*****s
发帖数: 1047
6
this one is more interesting
http://seekingalpha.com/article/1299691-aubagio-eu-backing-come
http://aishealth.com/blog/pharmacy-benefit-management/genzyme-m

【在 n*******n 的大作中提到】
: biogen idec 的吗?
A******y
发帖数: 2041
7
Never heard of Lyrica? VPA? Top sellers, no chemistry necessary. How about
Lithium...yum!

【在 n*******n 的大作中提到】
: biogen idec 的吗?
s*******q
发帖数: 81
8
一般神经系统的药物好象都是挺简单的小分子

【在 n*******n 的大作中提到】
: biogen idec 的吗?
1 (共1页)
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N,N-dimethyl-1-dodecanamine的测试方法据说是行凶的女教授: Amy Bishop
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相关话题的讨论汇总
话题: fda话题: drug话题: confirm话题: ms话题: fumarate