设为首页 加入收藏

TOP

Vesomni 6mg/0,4mg - Retard-Tabletten 索非那新/盐酸坦索罗辛复方缓释片
2014-12-08 23:50:19 来源: 作者: 【 】 浏览:1031次 评论:0
安斯泰来(Astellas)宣布,荷兰药品评价委员会(MEB)已批准了VESOMNI的上市许可申请(MAA),VESOMNI通过欧盟成员国相互互认程序方式获得批准。VESOMNI用于对单药疗法无足够响应的良性前列腺增生症(BPH)男性患者中度至重度储尿(storage symptoms)及排尿(voiding symptoms)困难的治疗。VESOMNI是一种每日一次,膀胱活动过度症治疗药solifenacin和BPH治疗药tamsulosin的固定剂量复合剂。其中tamsulosin 于2006年3月在欧洲失去专利保护。
索非那新/盐酸坦索罗辛复方缓释片

Product Name: VESOMNI 6 MG/0.4 MG MODIFIED RELEASE TABLETS

VESOMNI 6 mg/0,4 mg - Tabletten mit veraenderter Wirkstofffreisetzung XL.  - 135278 - ASTELLAS PHARMA EUROPE B.V., LEIDEN, NL-BE LEIDEN - ASTELLAS PHARMA GMBH, WIEN 

 
Vesomni: combination tablet for urinary storage symptoms associated with BPH
 
 
03 February 2014, 8:20am
 
Vesomni is a fixed-dose, modified-release combination tablet containing tamsulosin and solifenacin that is indicated for the treatment of moderate to severe storage symptoms and voiding symptoms associated with BPH, when the response to treatment with monotherapy is inadequate.

NICE recommends considering an anticholinergic in combination with an alpha-blocker for men who still have storage symptoms after treatment with an alpha-blocker alone.

 

PHARMACOLOGY

Tamsulosin is an alpha1 adrenoceptor antagonist that reduces smooth muscle tone in the prostate and bladder neck to increase urine flow. Solifenacin is a competitive and selective muscarinic receptor antagonist that reduces urinary urgency and frequency.1

CLINICAL STUDIES

The safety and efficacy of tamsulosin/solifenacin was established in the double-blind phase III NEPTUNE trial. The trial included 1,334 men who had storage and voiding lower urinary tract symptoms (LUTS) associated with BPH, defined as ≥2 urgency episodes per 24 hours, ≥8 micturitions in the 24 hours preceding randomisation, an International Prostate Symptom Score (IPSS) ≥13, a maximum urinary flow rate 4.0−12.0ml/s and a voided volume of ≥120ml during free flow.

Patients were randomised to receive placebo, a fixed-dose combination of tamsulosin and solifenacin, or tamsulosin alone for 12 weeks.2

Non-inferior to tamsulosin monotherapy

Combination therapy with 400 microgram tamsulosin plus solifenacin 6mg produced a significantly greater reduction from baseline than placebo in the primary endpoint, total IPSS [-7.0 vs -5.4 (p<0.001)], and was non-inferior to tamsulosin monotherapy for this endpoint (p=0.001; change from baseline -7.0 vs -6.2).2

The combination showed superiority to placebo and tamsulosin monotherapy in terms of the other primary endpoint, total urgency and frequency score (changes from baseline -8.1 vs -4.4 [p<0.001] and -6.7 [p<0.05], respectively).2

Improved quality of life

Patients receiving the combination tablet also reported significant improvements in IPSS and Overactive Bladder Questionnaire (OAB-q) quality of life scores (p<0.001 vs placebo; p<0.01 vs tamsulosin alone) and OAB-q sleep subscore (p<0.01 and p<0.05 vs placebo and tamsulosin, respectively).2

Tolerability

Tamsulosin/solifenacin was generally well tolerated. The most common adverse effects, including dry mouth, constipation and dyspepsia, reflect those typically associated with anticholinergics. Acute urinary retention was the most serious adverse effect but occurred in less than 1% of patients.1,2

NICE  recommendation

NICE recommends considering an anticholinergic in combination with an alpha-blocker for men who still have storage symptoms after treatment with an alpha-blocker alone.3

References:

  1. Vesomni Summary of Product Characteristics, October 2013.
  2. van Kerrebroeck P et al. Eur Urol 2013; 64: 1003–12.
  3. NICE Clinical Guideline 97 (May 2010). The management of lower urinary tract symptoms in men.

View Vesomni drug record










Registratienummer: RVG 111622
Registratienaam: Vesomni 6 mg/0,4 mg tabletten met gereguleerde afgifte
Procedurenummer: NL/H/2968/001
Farmaceutische vorm: Tablet met gereguleerde afgifte
Toedieningsweg: Oraal gebruik
ATC: G04CA53 - Tamsulosin and solifenacin
Afleverstatus: Uitsluitend recept
Registratiedatum: 06 mei 2013
Handelsvergunninghouder: Astellas Pharma Europe B.V.
  Sylviusweg 62
  2333 BE LEIDEN
   
SmPC: SmPC:  ( )
Patiëntenbijsluiter: Patiëntenbijsluiter:  ( )
Openbaar beoordelingsrapport: Openbaar beoordelingsrapport:  ( )
  Download Adobe Acrobat Reader


Werkzame stof(fen)
SOLIFENACINESUCCINAAT
SAMENSTELLING overeenkomend met
SOLIFENACINE
TAMSULOSINEHYDROCHLORIDE
SAMENSTELLING overeenkomend met
TAMSULOSINE
 


Hulpstof(fen)
BUTYLHYDROXYTOLUEEN (E 321)
HYPROMELLOSE (E 464)
IJZEROXIDE ROOD (E 172)
MACROGOL 7000000
MACROGOL 8000
MAGNESIUMSTEARAAT (E 572)
MALTOSE 0-WATER
MANNITOL (D-) (E 421)
SILICIUMDIOXIDE (E 551)
以下是“全球医药”详细资料
Tags: 责任编辑:admin
】【打印繁体】【投稿】【收藏】 【推荐】【举报】【评论】 【关闭】 【返回顶部
分享到QQ空间
分享到: 
上一篇Normosang 下一篇Xtandi 40 mg, capsule, zacht

相关栏目

最新文章

图片主题

热门文章

推荐文章

相关文章

广告位