Macluumaadka Daroogada Cudurka Cagaarshow C

Daroogada Isku-Dagaalladu waxay bixisaa Heerarka Dhiig-karka ee Genotype 1 iyo 4 Infekshannada

Qeybinta

Zepatier (elbasvir / grazoprevir) waa daroogo isku dhafan oo loo isticmaalo daaweynta infakshanka cagaarshow C (HCV) ee joogtada ah. Labada daawo ee ka kooban Zepatier (elbasvir, grazoprevir) waxay ku shaqeeyaan xakameynta labadaba borotiinka (NS5a) iyo enzym (NS3 / 4a protease) oo muhiim u ah soo-saarka fayraska.

Zepatier waxaa la ansixiyay 28-kii Juunyo 2016-ka Maamulka Maraykanka ee Cunta iyo Maandooriyaha (FDA) si loogu isticmaalo dadka waaweyn 18 sano ama ka badan HCV genotype 1 ama 4 infekshanka , oo ay ku jiraan kuwa qaba cirrhosis.

Waxaa loo ogolaaday isticmaalka labada daaweyn (daaweyn-naeef) ama hore loo daweeyey (daawayn khibrad leh) bukaanno, iyada oo ku xidhan Xeerka HCV iyo xaaladda daaweynta.

Waxtarka

Zepatier waxaa lagu soo waramayaa in ay leeyihiin heerar daaweyn oo heer sare ah oo ku jira marxaladda 2aad ee aadanaha. Daaweynta HCV waxaa lagu qeexay inay sii wadi karto culeyska fayruuska aan la ogaan karin muddo 24 toddobaad ah kadib marka la dhammeeyo daaweynta (oo loo yaqaanno jawaab celin joogta ah oo dheellitiran, ama SVR ).

Heerka guud ee SVR wuxuu u dhexeeyay 94% ilaa 97% bukaanada qaba HCV genotype 1, halka bukaanno qaba infekshanka 4-aad ee la soo wariyay ay sheegeen in ay leeyihiin heerka SVR oo ah 97% ilaa 100%.

Qiyaasta

Hal kiniin (50mg / 100mg) ayaa maalin walba la qaataa ama aan lahayn cunto. Kiniiniyada Zepatier waa nooc quruxsan, midab leh iyo filim qaboojiye leh, oo leh "770" daboolay hal dhinac.

Soo-jeedinta Talooyinka

Zepatier waxaa loo qoraa midkood ama aan lahayn ribavirin loogu talagalay cudurka genotype 1 ama 4. Si ka duwan sidii hore ee daaweynta HCV, peginterferon (daroogo la xidhiidha saameyn aan badneyn oo aan la dabooli karin) looma baahna.

Ka hor intaan la bilaabin daweynta, baaritaanka hidda-socodka ayaa la samayn karaa si loo go'aamiyo in aad leedahay nooca virus-ka oo u adkeysanaya qaybta elabvir ee Zepatier (oo loo yaqaanno NS5a-resistant-polymorphism).

Waqtiga daaweynta waxay u dhaxeysaa 12-16 asbuuc, taas oo ku xidhan HCV genotype iyo xaaladda daaweynta.

Genotype Xaaladda daaweynta Qaadashada
ribavirin?
Muddada
Genotype 1a daaweynta-naeef aan lahayn elbasvir-adkaysi
fayraska
maya 12 toddobaad
daaweyn-nadiif leh elbasvir-u adkaysta
fayraska
haa 16 toddobaad
horay loola dhaqmey ribavirin +
peginterferon iyada oo aan lahayn fayruska elbasvir-resistant
maya 12 toddobaad
horay loola dhaqmey ribavirin +
peginterferon fayruuska elbasvir-resistant
haa 16 toddobaad
horay loola dhaqmey ribavirin +
peginterferon + xanuunka HCV protease inhibitor ah
haa 12 toddobaad
Genotype 1b daaweyn-naeefan maya 12 toddobaad
horay loola dhaqmey ribavirin +
peginterferon
maya
12 toddobaad
horay loola dhaqmey ribavirin +
peginterferon + xanuunka HCV protease inhibitor *
haa 12 toddobaad
Genotype 4 daaweyn-naeefan maya 12 toddobaad
horay loola dhaqmey ribavirin +
peginterferon
haa 16 toddobaad

* - Olysio (simeprevir), Victrelis (boceprevir), Incivek (telaprevir)

Saameynada Caadiga ah

Waxyeellooyinka ugu badan ee la xiriira isticmaalka Zepatier (oo ku dhaco in ka badan 5% bukaanada) waa:

Marka la isticmaalo ribavirin, dhibaatooyinka daaweynta ee ugu badan ee la daaweeyey (oo ku dhaco in ka badan 5% bukaanada) waxaa ka mid ah:

Isdhexgalka daroogada

Daawooyinka soo socda waa in aan loo isticmaalin marka qaadashada Zepatier sababtoo ah waxay keeni karaan isdhexgalada mukhaadaraadka daroogada ee muhiimka ah:

Tixgelinta Daaweynta

Waxaa lagu soo bandhigay daraasad kiliinik ah in 1% bukaannada ku jira Zepatier ay sameeyeen heer sare oo ah unugyada beerka beerka oo muujinaya sunta sunta ah, guud ahaan ama ka dib isbuuca siddeedaad ee daaweynta. Sidaa daraadeed, baaritaanka dhiigga ee la xidhiidha beerka ayaa loo baahan yahay in la sameeyo ka hor inta aan la bilaabin daweynta iyo si joogto ah muddada daaweynta HCV.

Zepatier waa in aan loo qorin bukaanka qaba cillad beer culus.

Isticmaalka ribavirin wuxuu uur kudoon yahay uurka waana inaan lagu qorin Zepatier ama nooc kale oo cagaarshow C ah. Dumarka haweenka ku jira daaweynta ribavirin-ku salaysan waa in lagula taliyaa in ay ka fogaadaan uurka iyo inay isticmaalaan ugu yaraan laba hab oo hormoon ah oo ka hortagga uurka inta lagu jiro muddada daaweynta iyo lix bilood ka dib dhammaystirka daaweynta.

Xigasho:

Maamulka Cuntada iyo Dawooyinka Maraykanka (FDA). "FDA waxay ansixisay Zepatier si loogu daaweeyo cudurka cagaarshow C ee jilicsan 1 iyo 4." Silver Spring, Maryland; saxaafadeed la soo saarey January 28, 2016.

Merck. "Zepatier - Warbixinaha Wargelinta". Kenilworth, New Jersey; helitaanka Janaayo 29, 2016.