HRP20202070T1 - Tekuća neurotoksinska formulacija stabilizirana s triptofanom ili tirozinom - Google Patents

Tekuća neurotoksinska formulacija stabilizirana s triptofanom ili tirozinom Download PDF

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Publication number
HRP20202070T1
HRP20202070T1 HRP20202070TT HRP20202070T HRP20202070T1 HR P20202070 T1 HRP20202070 T1 HR P20202070T1 HR P20202070T T HRP20202070T T HR P20202070TT HR P20202070 T HRP20202070 T HR P20202070T HR P20202070 T1 HRP20202070 T1 HR P20202070T1
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Croatia
Prior art keywords
liquid preparation
botulinum neurotoxin
preparation according
disorders
tryptophan
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HRP20202070TT
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English (en)
Inventor
Anders Jarstad
Anna FRIIS
Ulf Stahl
Ann GURELL
Barbro AGREN
Emilia EDSTROM
Andrew Pickett
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Ipsen Biopharm Limited
Nestlé Skin Health Sa
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Application filed by Ipsen Biopharm Limited, Nestlé Skin Health Sa filed Critical Ipsen Biopharm Limited
Publication of HRP20202070T1 publication Critical patent/HRP20202070T1/hr

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    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
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    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/405Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
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    • A61K38/48Hydrolases (3) acting on peptide bonds (3.4)
    • A61K38/4886Metalloendopeptidases (3.4.24), e.g. collagenase
    • A61K38/4893Botulinum neurotoxin (3.4.24.69)
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Claims (18)

1. Tekući pripravak, naznačen time, što sadrži proteinski neurotoksin, tenzid, aminokiselinu odabranu od triptofana i tirozina, pufer koji sadrži natrijeve, kloridne i fosfatne ione, pri čemu navedeni tekući pripravak ima pH-vrijednost između 5,5 i 8, te pritom navedeni pripravak ne sadrži proteine izvedene iz životinja, i gdje je navedeni tekući pripravak stabilan u dužem vremenskom periodu.
2. Tekući pripravak prema patentnom zahtjevu 1, naznačen time, što je navedeni tenzid neionski tenzid.
3. Tekući pripravak prema patentnom zahtjevu 2, naznačen time, što navedeni neionski tenzid je polisorbat, poželjno polisorbat 20, polisorbat 60 ili polisorbat 80.
4. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 3, naznačen time, što navedena aminokiselina je triptofan, poželjno L- triptofan.
5. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 4, naznačen time, što navedeni pufer nadalje sadrži kalijeve ione.
6. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 5, naznačen time, što navedeni pripravak ima pH-vrijednost između 6,0 i 7,5.
7. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 6, naznačen time, što se ne događa više od 30% gubitaka u izvanstaničnoj proteolitskoj aktivnosti u dodatnom periodu od 2, 3, 6, 12, 18, 24 ili 36 mjeseci na 5 °C.
8. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time, što proteinski neurotoksin je botulinski neurotoksin, odabran od prirodnog botulinskog neurotoksina u obliku kompleksa, prirodnog botulinskog neurotoksina velike čistoće i rekombinantnog botulinskog neurotoksina.
9. Tekući pripravak prema patentnom zahtjevu 8, naznačen time, što navedeni botulinski neurotoksin je rekombinantni botulinski neurotoksin odabran od botulinskog neurotoksina A, B, C, D, E, F ili G, modificiranog botulinskog neurotoksina i kimernog botulinskog neurotoksina.
10. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 9, naznačen time, što navedeni tekući pripravak obuhvaća: • 4 do 10000 LD50 jedinica botulinskog neurotoksina po mL, • 0,001 do 15% v/v polisorbata, • 0,1 do 5 mg/mL triptofana, • 10 do 500 mM NaCl, • 1 do 50 mM KCl, • 1 do 100 mM natrijevog fosfata, te ima pH-vrijednost između 5,5 i 8, a stabilan je 6 mjeseci na 5 °C.
11. Tekući pripravak prema patentnom zahtjevu 10, naznačen time, što navedeni tekući pripravak obuhvaća: • 10 do 2000 LD50 jedinica botulinskog neurotoksina po mL, • 0,05 do 0,2% v/v polisorbata 80, • 0,1 do 5 mg/mL triptofana, • 25 do 300 mM NaCl, • 1 do 10 mM KCl, • 2 do 50 mM natrijevog fosfata, te ima pH vrijednost između 6,0 i 7,5, a stabilan je 12 mjeseci na 5 °C.
12. Tekući pripravak prema bilo kojem od patentnih zahtjeva 1 do 11, naznačen time, što se upotrebljava u liječenju.
13. Tekući pripravak prema patentnom zahtjevu 12, naznačen time, što se upotrebljava u liječenju ili prevenciji muskularnih poremećaja, neuromuskularnih poremećaja, neuroloških poremećaja, oftalmoloških poremećaja, poremećaja boli, psiholoških poremećaja, artikulacijskih poremećaja, upalnih poremećaja, endokrinih poremećaja ili uroloških poremećaja.
14. Uporaba tekućeg pripravka prema bilo kojem od patentnih zahtjeva 1 do 11, naznačena time, što je za estetsku medicinu, primjerice za obradu ili prevenciju naborane kože, posebice nabora na licu kao što su linije mrštenja lica, konturne bore oko očiju, horizontalne linije mrštenja na čelu, linije spuštenih usana, bore na vratu (platizmalne vrpce), bore na bradi (musculus mentalis, narančina kora, ulegnuta brada), naborane linije čela, bore kao „izgrebana koža“, obrada podizanja nosa ili linije bora od spavanja.
15. Uporaba aminokiseline odabrane od triptofana i tirozina, naznačena time, što služi za zaštitu proteinskih neurotoksina od propadanja, u tekućem pripravku u kojemu nema proteina izvedenih iz životinja.
16. Uporaba prema patentnom zahtjevu 15, naznačena time, što navedena aminokiselina je triptofan.
17. Uporaba prema patentnom zahtjevu 15 ili 16, naznačena time, što navedeni proteinski neurotoksin je botulinski neurotoksin.
18. Uporaba prema patentnom zahtjevu 15, naznačena time, što se navedena aminokiselina upotrebljava u kombinaciji s tenzidom i puferom koji sadrži natrijeve, kloridne i fosfatne ione, dok navedeni tekući pripravak ima pH-vrijednost između 5,5 i 8.
HRP20202070TT 2016-05-27 2020-12-28 Tekuća neurotoksinska formulacija stabilizirana s triptofanom ili tirozinom HRP20202070T1 (hr)

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Application Number Priority Date Filing Date Title
EP2016062085 2016-05-27
PCT/EP2017/062785 WO2017203038A1 (en) 2016-05-27 2017-05-26 Liquid neurotoxin formulation stabilized with tryptophan or tyrosine
EP17728095.5A EP3463432B1 (en) 2016-05-27 2017-05-26 Liquid neurotoxin formulation stabilized with tryptophan or tyrosine

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US (4) US20190183988A1 (hr)
EP (3) EP3463432B1 (hr)
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