Liphetho tse Ncha tse Ntle bakeng sa Phekolo ea Psoriatic Arthritis

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ngotsoeng ke Linda Hohnholz

ACELYRIN, INC., Affibody AB, le Inmagene Biopharmaceuticals Co., Ltd., kajeno ba phatlalalitse hore teko ea bongaka ea libeke tse 16, ea lefats'e, ea Phase 2 ea izokibep ho bakuli ba 135 ba nang le psoriatic arthritis (PsA) e fihletse pheletso ea eona ea mantlha ea ACR50. Izokibep e boetse e fihletse liphetho tsa bobeli, ho kenyeletsoa karabelo ea PASI, ntlafatso ea li-LEED tsa enthesitis, le ntlafatso ea boleng ba bophelo ho sesebelisoa sa bophelo se netefalitsoeng sa PsA-specific, lethathamo la lipotso tsa Psoriatic Impact of Disease (PsAID).   

Teko ea tleliniki e sa sebetseng e sa boneng habeli, e laoloang ke placebo, ea Phase 2 e ile ea lekola polokeho le katleho ea izokibep e fuoa 80 mg libeke tse ling le tse ling tse peli (Q2W) kapa 40 mg Q2W, khahlano le placebo Q2W, ho bakuli ba baholo ba nang le PsA e sebetsang. Qetello ea mantlha ea ACR50 le ea bobeli ea likarabo tsa PASI li ile tsa finyelloa 'me li ne li le ka holimo ho mefuta e mengata ea likarabo, ha li bapisoa le se tlalehiloeng bakeng sa meriana e meng e amohelehang kapa e nts'etsopele bakeng sa PsA. Palo ea bakuli ba nang le tharollo ea enthesitis e bonahala e fapane. Ntlafatso e nang le morero oa bophelo bo botle ba bophelo bo tobileng bo ile ba finyelloa ka tekanyo ea sephetho se tlalehiloeng ke mokuli, PsAID. Ha ho mathata a macha a tšireletso a ileng a tsejoa.

"Lintlha tse ntle tse hlahisitsoeng tekong ena ea Phase 2 li tšehetsa khopolo ea rona ea hore potency e phahameng le boholo ba limolek'hule tse nyenyane tsa izokibep li fella ka menyetla ea ho pepeseha ho hoholo, ka hona, katleho e kholoanyane. Kenello e matlafalitsoeng ea lithethefatsi ka har'a lisele tse teteaneng, tse se nang vascularized entheseal e ne e tla lumellana le phokotso e kholoanyane ea bohloko bo bonoang ka kalafo ea izokibep," ho boletse Paul Peloso, MD, ofisiri e kholo ea bongaka (CMO) ea ACELYRIN.

"Mahlaba a setseng a entheseal a amahanngoa le lefu le matla le ho fokola ha bophelo. Hoa thabisa ho bona tharollo e ntlafetseng hakana ea lefu la ho ruruha ha mokokotlo le boemo ba bophelo bo ntlafetseng ba bakuli, "a phaella ka ho re.

“Psoriatic arthritis ke lefu le ruruhileng le bohloko le le fokolisang la manonyeletso, letlalo le manala, hape le ka ama lesapo la mokokotlo. Re thabetse teko ena ea Phase 2 e totobatsang bokhoni ba izokibep ho fana ka katleho e fapaneng ea bongaka sebakeng sena sa tlhoko e tsoelang pele e sa fihlelleheng, "ho boletse Prof. Nikolai Brun, MD, PhD, CMO of Affibody. "Habohlokoa, monyetla o sa ntse o le teng oa ho tsoela pele ho hlahloba menyetla e phahameng ea ho ntlafatsa karabelo le ho fana ka izokibep e le ente e le 'ngoe ea SC."

Shao-Lee Lin, MD, PhD, mothehi-mmoho le CEO oa ACELYRIN, o itse, "Lintlha tsena li tiisa kholiseho ea rona leanong le phatlalalitsoeng pele la ho lekola ka botlalo bokhoni ba thibelo ea IL-17A bakeng sa katleho ea phetoho libakeng tse ngata tsa mafu."

"Lintlha tsa PsA P2 li na le litlamorao tse ntle haholo-holo bakeng sa axial spondyloarthritis (AxSpA) le psoriasis (PsO), e fuoeng tšusumetso ho enthesitis le likarabo tsa PASI. Dosing e phahameng (160mg QW) le Q2W dosing ea izokibep li tla ithutoa boithutong ba bohlokoa ba PsA P2b/3 e le mohato o latelang oa ntšetso-pele ea lenaneo," a eketsa.

David Bejker, CEO oa Affibody, o itse, "Liphetho tsena tsa boithuto li bohlokoa ho bonts'a monyetla oa ho theha metsoako ea maemo a holimo ho latela theknoloji ea Affibody®."

Lintlha tsa lintlha tsa teko ea PsA Phase 2 li tla arolelanoa ka pontšo ea sethala ho European Alliance of Associations for Rheumatology Congress (EULAR) Congress e Copenhagen ka June 3, 2022, ka 11:05AM CET.

ACELYRIN e na le litokelo tsa lefats'e tsa izokibep ntle le litokelo tsa nts'etsopele le khoebo ka Inmagene linaheng tse khethiloeng tsa Asia, ho kenyeletsoa Chaena, Hong Kong, Korea Boroa le Taiwan, le ho sa kenyelelitsoe Japane. Affibody o na le litokelo tsa khoebo linaheng tsa Nordic.

SEO U LOKELANG HO SE NKA HO SEHLOOHO ENA:

  • The primary endpoint of ACR50 and secondary endpoint of PASI responses were met and were at the top of the range of responses, compared to what has been reported for other medicines approved or in development for PsA.
  • Higher dosing (160mg QW) and Q2W dosing of izokibep will be studied in a PsA P2b/3 pivotal study as a next step in advancement of the program,”.
  • Details of the PsA Phase 2 trial data will be shared by podium presentation at the European Alliance of Associations for Rheumatology (EULAR) Congress in Copenhagen on June 3, 2022, at 11.

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Linda Hohnholz

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