HUE034005T2 - Terápiák tüdõfunkció javítására - Google Patents
Terápiák tüdõfunkció javítására Download PDFInfo
- Publication number
- HUE034005T2 HUE034005T2 HUE11769881A HUE11769881A HUE034005T2 HU E034005 T2 HUE034005 T2 HU E034005T2 HU E11769881 A HUE11769881 A HU E11769881A HU E11769881 A HUE11769881 A HU E11769881A HU E034005 T2 HUE034005 T2 HU E034005T2
- Authority
- HU
- Hungary
- Prior art keywords
- gly
- ser
- val
- thr
- seq
- Prior art date
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- C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
- C07K16/244—Interleukins [IL]
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- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
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- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- A—HUMAN NECESSITIES
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6863—Cytokines, i.e. immune system proteins modifying a biological response such as cell growth proliferation or differentiation, e.g. TNF, CNF, GM-CSF, lymphotoxin, MIF or their receptors
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- A—HUMAN NECESSITIES
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- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
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- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
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Claims (4)
- teeâîN Tüpar«€|ô mÄIäa Bkalsitlkipd igésyjíöHíek î> ftsÂsàbaa töttésö: alfeámű#$s -ÄiU :Âifté!ybe%: 'fel ·«?· :1E>.||-St^ag#íjiii^: ^OJtÉSili^P sSe»i vilest vagy ftnmln. IWik-sí: iiötö Împ;SSSiîs: áíneiy #: kővetkezők:: alkotta ösopoKb# válasxíoít: Cfi) h^Ä ÍL-Í3 AjI tmtíiest vsuí.toáí3tíM.iíW fcjgtrien«* amely fcotalm&z HOOK!-et. HCDR2-Î e» táftaimáxő VH-dsmént és IU'JûM-s% LCDRÏ-t és l..CDR3-at t&tt.t]roaz6 VI »dombot ahoi a HCÖH 5 sœtossy-siækv^eiâjs & SE#:$£NO: 7 s^M ^d^eaftia, s ΙΙ£0Η2 am?nosftv..s?«kveniqia a SEQ SI) NO: 8 szeribti szekvencia. a HCDR3 s-ninoxav-szekvenciája a SBÇ SD NO: §'^«#sI'sÄVeöcia. ax LCOE1 aminosav-székvenoiap a SEQ10 NO: !0 szerinti szekwiie%^ a SEQ ID NO: O szerit«! szekvencia,, es axliOIM^asiaoxïv^œkvejKiàjü alE^lDNO: 12 sgointi szgkveocla; (b) humán 11,0 3 efeí aÂstvagy humán SL· >a:W iipstîM, amely tartalmaz VH-domcot, amelynek asnino»· »awvSi^kvaiîcléls a SEQ SO NO: S 7 szerinti szekvmÄ èf ypAts amdipek amlaöpv^zskvsnciála a SEQ TD NÖ: 16 szerinti szekvencia; és <c>axta) vagy (b) szerinti, knnán 11,03 elleni amitest vagy hamun 11 O) a^y^lmaæ.«b-· ba humán tgG4 konstans dément; alíöl a m#Ssik6Í6bas} t^ksysÉ®# j»0$ «κ yiiltelaöskíiépasí s#so#eyctér%at (#«sy Ex^^-Voii^· One.8%javulj -|ttmÉt IL· O elleni sÄst vagy kaÄ WM MH ts;|Mas#éáífca 6!Őti Mvétt- aiapvotsai-PEVOot^éshcs képest: és aboi tsz IL-B-antstesí vagy anoak ΙΜ:3»«ί Mi:l^p)pa^lbÂii,iSRtbkuiàa történik 100-600 mg dózisban. % A& I,:lgfeypbtsg6t|ä5ti IL - 13-anísgomsta ax ott meghatározott alkalmazásra. ahol ax antagonist» a keveE kezők: alkPka csoporSMl váSáSxibít: »nmungkásubn-moiekuía. ntonoRfctnálK antkm.i, kimera antitest, CDEpaitöit antitest, Irnrnanizästaetitest, Fäb, Fabk F(ab')j, iNpIsztiiikkkspcxolt Fv. scFv, diatest. rnaUtspecilleus· antitest, dnálls: spcillkus antitest IsiSiap^títes aftlítesL & Az: előző Igénypontok báPPbjyíke sísösMI :^Ι3^ίδηοηΐ8;η az ott useghatároxeá aikaismtxásca, altöl a sxe~ 'málytté^iSSSÉnávai« CÖPD-vel vagy idiopátlás tüdöilbróxíssal asszociált sértik tüdôbmdôja « 4; Az előzd igénypontok bármelyike szerinti IL-ïà-aatagoaista az ott meghattesöit alkalmazásra, ahol a sxe-mélynek a kővetkezők közöl választott asztmával asszociált sémii tudöftmkdéja van: atőpiás máim, sem: stógiáx assto^gnyhátől a súlyosig katikpszísroídök âiiïil áenr kpoktsíláít»: enyhétől a súlyosig terjedő asztma és 5,4. a, 2 vagy 1 GÏNA'poniéttéku asztma, SI M előző igénypontok bátmeiyüce szerinti rLOI-antagonista a?, od meghautmzott aikabnazásttk aböl: a személynek as^iïtârfaàiÂilAétlllt: tlldőlMkösőía vak, es cgykletöieg a köveikexok. kökbl választott: egy : vagy több további terápiás SKPtrei tblyáateiy teráplábao :vesxityskt: béléisgxed koőlkesAesokl, hosszan, ható bdiádEittnagoalsta rkABAk HVïOUin. letikotriéiKintstgonista ér orátis komkosztmrid : i> A» eldxő: ^y^nttÉ!:jfeliS#iiíé #^Ä:*p^bNg^sia. az olt meghatározott slMlnwásra, tiokaz: IE-IS-atkítést: vagy ánoák: ILrís^at kötő %g3rsépse bsikihsk sxhbktbáti tiileoik a kövptkoxb dózisok alkotta csopottbői válas;;<tott ckobsban: 13(1 mg. 300 mg és 6(k? mg. 7. lgié?í^!^!^.0k tkktS^ntagíMiíStá ax pit aseghatározött alkalrnîtzssog abokax:!,- 13 «liest vagy áopak II,-13%ötő trápteőSé a;lidyetkepk:|ök6i: väigsxtiSt gyakorisággal kerül Ijeadástp: h % 3,^:4 ·% 10 és 12 hetemé §·.· Az sïôaô igénypontok. bármelyike szeáhEtMI-ant^omsta a?, öitmej^atárözött·aJkslmázástUj alsói a Oklo-•fenkdőban bekövetkező javulás: as asídmás személyekben a kezelés kezddé föl ksimtkstt· -I $ »φρ&Ι. klmnfeötátb;. 9. A:?: előző igénypontok bármelyike szerinti ít-jS^bfegemstá az ott á:cgmgám;mí:; áltomeáiásrá, áhbl & lÁlö-.fitnkcióban bekövetkező javulás sa asztmás $z&ixá*$<M%é a kezelés besamtoésétél számított legalább 12 hétté! ki-ímsístkató. iö. Az I-E, .Igénypontok bámélylkexszethiti IL43-aöi:ágönísí8 sa ok meeiístáíxía-.oö aiMnutdm. «höl az íL"J3'-íííkitoss vagy taxttak .11,-13-¾ kőtS iksgmnoss beadásé -szukkuton torténlk '300 mg díQlsÍJsn 2 hetes •vagy 4 hetes beadási iíítorvullunKskban.
- 11. Az I -9. igénypontok bármelyike szennö ÎL* 1S-nofegóftisfe az ptt' rneghafendt*· alkalmndta, ahol a ladik iunkdébas bekövetkező javulás FEV; pontértékben bekövetkezett 8~iő% javulás- a humán IL" 13 elleni antitest vagy •annak humán lL-l3-:á kösö ihrçpnense- kéthetes- vagy négyfesfes imerv&líumekban történő -szubkofen. 'beadása előtt, felvéti alapvonul-FEV 1 -mérésbe;?, képest.
- 12. Az 1-9. igénypontokbármelyike szerínEIL-ll-antagötásta-axott meghatározott: »Ikstaasátsra, aboi a tüdő-fenkdóbanbekövetkező javulás FEV I pout&tckbm;baköv«teaeiI -iS-^^javulfeahumáh IL-13 elkftl antitest' vagy annak humán IL-D-atkötö ßsgmense szufckuíán beadása êlêttfelvétt--álapv©tto.|>-FE¥l'-métáshe&képssk
- 13. Az 1-5, igénypontok bármelyike s«örlníl IL-D-anlagonlsta .az ott meghatározott alkalmadra, altol a fedő-ftmkdöban bekövetkező javulás FEY1 pontértékben bekövetkezett .8% javulás ISO mg hunién IL--I3 elleni antitest, vagy .humán II.·-13-as kötő fiagmess kéthetes inmalteökfeíta történő szifekután bssslásss élőit felvált aispwnal· FÉYfeméréshez képest, vagy aboi a íüdőfimkctóbaa bekövetkező javulás FEVUpoaiénékbéa bekövetkező 13,3% javulás 3ŐÖ .mg barnán 1L-I3 •elleni antitest vagy humán lL-L3-at kőtő fragmetts kéthetes inteivaflumokhaa történő -szabkután beadása elölt felvett, alapvonal FEV Î-méréshez képest, vagy •ahol a tudőfenkoióhaa bekövetkező javulás FEVi-pontértékben bekövetkező IS.2% javulás őÖ6 .mg. humán íL-!3 elleni antitest vagy annak barnán ÏL- LMs kőtó ftogmettse· kéthetes .latetvallumokban történő szubkufen beadása előtt fölvett: alapvonal· FEV i-méréshez képest·. .14. Az előző igénypontok· bármelyike: szerinti: ÜL- l>sntogonista. .az tát .meghatározott alkáSmazásm, ahol az ÍLQ3-antagomst» humán 11..-1 .> «ltom antitest. vagy annak humán IL-J3-ss kösd 'Supsense, amely tartalmaz HCP.RI -eu HCDR2-f és HCDR3-»t tartalmazó VH-dotnént és LCEIEJ-st, LCDlO-i és LCDR3-st tostshuisssl VL«doménú ahol a EICDR1 amhuesawszekvenclája: & SEQ1DKÖ: ? szemű szekvssnsila, a HCDR2 amlnosav-«2eky«nçjàj& a SBQ! II) NO: :8 smmti szekvencia, a MEDIO ítsölösisav-szdívendspa .a SEQ 113 'NO: 9 szerinti szekvencia, az LC.PRI amlnosav^szekvenetá|a a SEQ ÍD HÖ.: 10 szerinti ssekvenda, az. I.CDR2: amin<sav-szekvenoláj.a. a SEQ ID NO: 11 szerinti szekvencia,.és az S..CDR3 amirsosav-szekvendája a SEQ ID M3:: 12 sz^ilnd szekvencia. IS. Az· előző tgény^mmok bánnelylke· szítod ΙΙ,-13-sstagonlsta az olt nieghsOmz.«» alMmszásm, sböl az ll..-l3-a«ïagofi!,s'ta humfet ií.-O elleni anólesi vagy amtdt humán ίΕ-13-aî: kGő Ihapnzuse, amely ptrtalingz VI-|-domént, amelynek aminosav-szek\anci#a-a SEQ 03 NO: IS .szerk-íl szekvenda és Vl,-doméírt. amelynek amlmsav* Sixíkvendája a SEQ .03 NO: 16 szerinti szekvencia. lő. Az előző Igénypontok hfenelylke szsíiatl 1L-13-anlagonista az ott aK'ghatEfosoll alkalmadra, altul a UF döfunketÄm hekövefeezó javulás a EEVI pontértékben bekövetkezett 5-12% javulás a humán 1I.-13 ellent antitest vagy annak humán IL' 13-aí kbtő Eagmense szubkután beadásá-elótt felvett alapvonal-EBV 1-mété^tez.képest
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| RU2690675C2 (ru) | 2012-08-21 | 2019-06-05 | Санофи Байотекнолоджи | Способы лечения или предотвращения астмы посредством введения антагониста il-4r |
| EP3485902A1 (en) * | 2013-10-15 | 2019-05-22 | Astrazeneca AB | Methods for treating chronic obstructive pulmonary disease using benralizumab |
| AU2015209124A1 (en) * | 2014-01-27 | 2016-08-18 | Medimmune, Llc | Dipeptidyl peptidase-4 (DPP4/CD26) as a peripheral biomarker of IL-13 activation in asthmatic lung |
| IL315136A (en) * | 2014-02-21 | 2024-10-01 | Sanofi Biotechnology | Methods for treating or preventing asthma by administering an il-4rantagonist |
| AU2015246037B2 (en) | 2014-04-11 | 2018-04-12 | Novartis Ag | Methods of selectively treating asthma using IL-13 antagonists |
| EP3242686B1 (en) | 2015-01-09 | 2020-07-08 | Medimmune, LLC | Assay to detect human dpp-4 |
| CN104605857A (zh) * | 2015-02-12 | 2015-05-13 | 上海朔茂网络科技有限公司 | 一种肺功能测量方法 |
| PL3448391T3 (pl) | 2016-04-27 | 2024-09-16 | AbbVie Manufacturing Management Unlimited Company | Sposoby leczenia chorób, w których jest szkodliwa aktywność il-13, przy zastosowaniu przeciwciała anty-il-13 |
| CN112057419B (zh) * | 2017-03-01 | 2023-08-22 | 免疫医疗有限公司 | 单克隆抗体的配制品 |
| WO2019028367A1 (en) | 2017-08-04 | 2019-02-07 | Regeneron Pharmaceuticals, Inc. | METHODS OF TREATING ESOPHAGITIS WITH ACTIVE EOSINOPHILES |
| EP3935085A1 (en) | 2019-03-06 | 2022-01-12 | Regeneron Pharmaceuticals, Inc. | Il-4/il-13 pathway inhibitors for enhanced efficacy in treating cancer |
| PH12021552123A1 (en) | 2019-03-21 | 2022-08-22 | Regeneron Pharma | Combination of il-4/il-13 pathway inhibitors and plasma cell ablation for treating allergy |
| JP7592064B2 (ja) | 2019-07-16 | 2024-11-29 | サノフィ・バイオテクノロジー | Il-4rアンタゴニストを投与することにより喘息を治療するまたは予防するための方法 |
| CN116157688A (zh) * | 2020-07-31 | 2023-05-23 | 基因泰克公司 | 用于治疗炎症性呼吸系统疾病的恶化的方法 |
| CN112341543B (zh) * | 2021-01-11 | 2021-04-23 | 广东赛尔生物科技有限公司 | 包含间充质干细胞外泌体的药物组合物在治疗疾病中的应用 |
| WO2023130010A1 (en) | 2021-12-30 | 2023-07-06 | Regeneron Pharmaceuticals, Inc. | Methods for attenuating atopic march by administering an il-4/il-13 antagonist |
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| CA2140660A1 (en) * | 1993-06-13 | 1994-12-22 | Uwe R. Juergens | Use of terpene compounds for reduced release of arachidonic acid and of inflammation mediators |
| GB0004016D0 (en) | 2000-02-22 | 2000-04-12 | Royal Brompton Hospital | Biological material and uses thereof |
| GB0407315D0 (en) | 2003-07-15 | 2004-05-05 | Cambridge Antibody Tech | Human antibody molecules |
| CA2587903A1 (en) * | 2004-11-17 | 2006-05-26 | Amgen Fremont Inc. | Fully human monoclonal antibodies to il-13 |
| GB0600488D0 (en) * | 2006-01-11 | 2006-02-22 | Glaxo Group Ltd | Immunoglobulins |
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| EP2627673A1 (en) | 2013-08-21 |
| ES2645368T3 (es) | 2017-12-05 |
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| CA2814431A1 (en) | 2012-04-19 |
| CN103328506A (zh) | 2013-09-25 |
| EP2627673B1 (en) | 2017-07-26 |
| MX2013004212A (es) | 2013-09-02 |
| AU2011315499A1 (en) | 2013-05-02 |
| PL2627673T3 (pl) | 2018-01-31 |
| JP2013544235A (ja) | 2013-12-12 |
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