 |
 |
 |
 |
 |
 |
||
 |
 |
 |
 |
 |
| 1 | 1/1 | 返回列表 |
| 查看: 606 | 回復(fù): 0 | ||
[資源]
糖尿病新靶點(diǎn)藥物-SGLT-2抑制劑Dapagliflozin Rejected by F.D.A. Panel
|
|
AstraZeneca and Bristol-Myers Squibb Company today reported the outcome of the US Food and Drug Administration's (FDA) Endocrinologic and Metabolic Drugs Advisory Committee meeting on the New Drug Application for the investigational compound dapagliflozin. On the question: "Do the efficacy and safety data provide substantial evidence to support approval of dapagliflozin as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus?", the Advisory Committee voted 6 yes and 9 no. Bristol-Myers Squibb and AstraZeneca remain committed to the dapagliflozin clinical development programme and will continue to work closely with the FDA to support the review of this investigational compound. Dapagliflozin is under joint development by Bristol-Myers Squibb and AstraZeneca. Dapagliflozin is being investigated as monotherapy in addition to diet and exercise, and in combination with other anti-diabetic agents in addition to diet and exercise, to evaluate its effect on blood sugar levels (or HbA1c) in adults with type 2 diabetes. Dapagliflozin, an inhibitor of SGLT2, a target in the kidney, would potentially be the first in a new class of insulin-independent, oral type 2 diabetes agents. The FDA Endocrinologic and Metabolic Drugs Advisory Committee based its voting on a review of data from the comprehensive dapagliflozin global clinical development programme included as part of the FDA New Drug Application submission. This submission included data of up to two years in duration and involved approximately 6,000 individuals in 40 clinical studies. The trials were designed to evaluate the safety, tolerability and efficacy (as measured by HbA1c) of dapagliflozin in the approximately 4,200 patients who received dapagliflozin and were at various stages of the continuum of type 2 diabetes. In accordance with FDA guidelines, the New Drug Application also included data assessing the cardiovascular safety of dapagliflozin in adults with type 2 diabetes. The FDA is not bound by the Advisory Committee's recommendation but takes its advice into consideration when reviewing New Drug Applications. The Prescription Drug User Fee Act (PDUFA) goal date for dapagliflozin is 28 October 2011. NOTES TO EDITORS About Type 2 Diabetes In 2010, diabetes was estimated to affect nearly 300 million people aged 20 - 79 worldwide. Because of the aging population and the growing trend of obesity, the prevalence of diabetes is projected to reach nearly 440 million by 2030. Type 2 diabetes accounts for approximately 90 - 95% of all cases of diagnosed diabetes in adults. Type 2 diabetes is a chronic, progressive disease characterised by insulin resistance and/or dysfunction of beta cells in the pancreas, which decreases insulin sensitivity and secretion, leading to elevated glucose levels. Over time, this sustained hyperglycemia contributes to worsening insulin resistance and further beta cell dysfunction. To date, treatments for type 2 diabetes have focused primarily on insulin-dependent mechanisms. An approach that acts independently of insulin could provide an additional option for adults with type 2 diabetes. Significant unmet needs exist as nearly half of treated patients remain uncontrolled on their current glucose-lowering regimen. Many patients with type 2 diabetes have additional co-morbidities (such as obesity) which may complicate glycemic control. About SGLT2 Inhibition The kidney plays an important role in glucose balance, normally filtering ~180g of glucose each day, with virtually all glucose being reabsorbed back into circulation. SGLT2 is the major sodium-glucose cotransporter in the kidney and is an insulin-independent pathway for the reabsorption of glucose back into the blood. 、 |
回復(fù)此樓» 猜你喜歡
349藥學(xué)專碩105500求調(diào)劑
已經(jīng)有1人回復(fù)
-
求調(diào)劑
已經(jīng)有1人回復(fù)
-
藥物學(xué)論文潤色/翻譯怎么收費(fèi)?
已經(jīng)有262人回復(fù)
-
298求調(diào)劑一志愿中海洋
已經(jīng)有3人回復(fù)
-
藥學(xué)調(diào)劑申請(qǐng)自薦信，一志愿中南大學(xué)
已經(jīng)有1人回復(fù)
-
藥學(xué)349專碩求調(diào)劑
已經(jīng)有1人回復(fù)
-
《左乙拉西坦注射液制備工藝研究、質(zhì)量控制和穩(wěn)定性研究》下載
已經(jīng)有1人回復(fù)
-
105500藥學(xué)求調(diào)劑，一志愿山東大學(xué)藥學(xué)，348分
已經(jīng)有3人回復(fù)
-
考試
已經(jīng)有2人回復(fù)
找到一些相關(guān)的精華帖子，希望有用哦~
【課件】天然藥物化學(xué)（華中科技大學(xué)）
已經(jīng)有275人回復(fù)
- 博士點(diǎn)基金的到賬時(shí)間
已經(jīng)有6人回復(fù)
- 要不要轉(zhuǎn)2+3博士 藥物化學(xué)專業(yè)
已經(jīng)有15人回復(fù)
- 有機(jī)合成，藥物化學(xué)，文章影響因子數(shù)
已經(jīng)有15人回復(fù)
- 【習(xí)題資源】藥物化學(xué)習(xí)題
已經(jīng)有54人回復(fù)
- 分子靶向抗腫瘤藥物研究進(jìn)展
已經(jīng)有188人回復(fù)
- 【納米醫(yī)學(xué)】夏幼南最新一篇關(guān)于靶向藥物的報(bào)道
已經(jīng)有119人回復(fù)
點(diǎn)擊這里搜索更多相關(guān)資源科研從小木蟲開始，人人為我，我為人人
相關(guān)版塊跳轉(zhuǎn)
我要訂閱樓主 091602 的主題更新
| 1 | 1/1 | 返回列表 |
| 最具人氣熱帖推薦 [查看全部] | 作者 | 回/看 | 最后發(fā)表 | |
|---|---|---|---|---|
|
[考研] 一志愿085600中科院寧波所276分求調(diào)劑 +4 | 材料學(xué)257求調(diào)劑 2026-03-28 | 5/250 |
|
|---|---|---|---|---|
|
[考研] 367求調(diào)劑 +5 | 芋泥啵�！� 2026-03-28 | 5/250 |
|
|
|
[考研] 一志愿南開大學(xué)0710生物學(xué)359求調(diào)劑 +5 | 兔兔兔111223314 2026-03-29 | 7/350 |
|
|
|
[考研] 284求調(diào)劑 +14 | junqihahaha 2026-03-26 | 15/750 |
|
|
|
[考研] 295求調(diào)劑 +5 | wei-5 2026-03-26 | 5/250 |
|
|
|
[考研] 279求調(diào)劑 +4 | 蝶舞輕繞 2026-03-29 | 4/200 |
|
|
|
[考研] 本科新能源科學(xué)與工程，一志愿華理能動(dòng)285求調(diào)劑 +7 | AZMK 2026-03-28 | 11/550 |
|
|
|
[考研] 求調(diào)劑 +6 | 蘆lty 2026-03-25 | 7/350 |
|
|
|
[考研] 調(diào)劑 +3 | 好好讀書。 2026-03-28 | 3/150 |
|
|
|
[考研] 331環(huán)境科學(xué)與工程求調(diào)劑 +3 | 熠然好運(yùn)氣 2026-03-27 | 3/150 |
|
|
|
[考研] 265求調(diào)劑11408 +3 | 劉小鹿lu 2026-03-27 | 3/150 |
|
|
|
[考研] 274求調(diào)劑 +17 | 顧九笙要謙虛 2026-03-24 | 23/1150 |
|
|
|
[考研] 材料求調(diào)劑 +5 | .m.. 2026-03-25 | 5/250 |
|
|
|
[考研] 中國科學(xué)院深圳先進(jìn)技術(shù)研究院-光纖傳感課題組招生-中國科學(xué)院大學(xué)、深圳理工大學(xué)聯(lián)培 +5 | YangTyu1 2026-03-26 | 5/250 |
|
|
|
[考研] 309求調(diào)劑 +4 | gajsj 2026-03-25 | 5/250 |
|
|
|
[考研] 各位老師您好：本人初試372分 +5 | jj涌77 2026-03-25 | 6/300 |
|
|
|
[考研] 求調(diào)劑 +3 | 李李不服輸 2026-03-25 | 3/150 |
|
|
|
[考研] 一志愿武理085500機(jī)械專業(yè)總分300求調(diào)劑 +3 | an10101 2026-03-24 | 7/350 |
|
|
|
[考研] 300分，材料，求調(diào)劑，英一數(shù)二 +5 | 超贊的 2026-03-24 | 5/250 |
|
|
|
[考研]
085404電子信息284分求調(diào)劑
+4
|
13659058978 2026-03-24 | 4/200 |
|