Abrocitinib

Whakaahuatanga Poto:

Ingoa API Tohutohu Kaihanga hou Te Ra Whakamutunga Patent(Te US)
Abrocitinib Dermatitis Atopic Pfizer Feb.11, 2034


Taipitopito Hua

Tohu Hua

WHAKAMAHI HUA

Ko te Abrocitinib te waha, te ngota ngota iti, Janus kinase (JAK) 1 te aukati i te whakawhanaketanga mo te maimoatanga o nga pakeke me nga taiohi me te ahua o te mate pukupuku o te mate pukupuku.

Kei te tirotirohia a Abrocitinib i te whakamatautau haumanu NCT03796676 (JAK1 Inhibitor With Medicated Topical Therapy i roto i nga taiohi me te Atopic Dermatitis).

Ko te Abrocitinib kei te whakawhanakehia e Pfizer mo te maimoatanga o te mate mate pukupuku (eczema).He kai whakatewhatewha a-waha kotahi ia ra, Janus kinase 1 (JAK1).

Ko te mate pukupuku Atopic (AD) he mate kiri uaua, mau tonu, mumura e tohuhia ana e te pruritic, te tino patito, me nga rei eczematous e pa ana ki te 25% o nga tamariki me te 2% ki te 3% o nga pakeke o te ao.Ko te Abrocitinib he aukati whiriwhiri o Janus kinase-1 (JAK1) whākōkī e aukati ana i te tukanga mumura.Na reira, i whai maatau ki te aromatawai i te kaha me te haumaru o te abrocitinib mo te AD ahua-ki-paakaha.

Ko te Abrocitinib i roto i te horopeta 100 mg, 200 mg ranei he rongoa whai hua, he pai te whakamana, me te whai hua mo te rongoa i nga turoro me te mate mate pukupuku ahua-ki-maha.Heoi, i pai te tātaritanga ki te whaihua o te abrocitinib 200 mg i runga i te 100 mg, engari ka nui ake nga paanga o te taha penei i te nausea me te mahunga ki te 200 mg.

Tiwhikete

2018 GMP-2
原料药GMP证书201811(captopril ,thalidomide etc)
GMP-of-PMDA-in-Chanyoo-平成28年08月03日 Nantong-Chanyoo-Pharmatech-Co
FDA-EIR-Letter-201901

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