HRP20210749T1 - Farmaceutski pripravci koji sadrže azd9291 - Google Patents

Farmaceutski pripravci koji sadrže azd9291 Download PDF

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Publication number
HRP20210749T1
HRP20210749T1 HRP20210749TT HRP20210749T HRP20210749T1 HR P20210749 T1 HRP20210749 T1 HR P20210749T1 HR P20210749T T HRP20210749T T HR P20210749TT HR P20210749 T HRP20210749 T HR P20210749T HR P20210749 T1 HRP20210749 T1 HR P20210749T1
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Croatia
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pharmaceutical
parts
pharmaceutical preparation
preparation according
diluents
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HRP20210749TT
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English (en)
Inventor
David Wilson
Cindy FINNIE
Steven Anthony Raw
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Astrazeneca Ab
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=50191689&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20210749(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of HRP20210749T1 publication Critical patent/HRP20210749T1/hr

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physiology (AREA)
  • Nutrition Science (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Claims (18)

1. Farmaceutski pripravak koji sadrži: (a) od 2 do 70 dijelova Sredstva; (b) od 5 do 96 dijelova dva ili više farmaceutskih razrjeđivača; (c) od 2 do 15 dijelova jednog ili više farmaceutskih sredstava za raspadanje; (d) od 0 do 0,75 dijelova jednog ili više farmaceutskih sredstava za topivost; i (e) od 0,5 do 3 dijela jednog ili više farmaceutskih sredstava za povećanje skliskosti; pri čemu svi dijelovi su maseni i zbroj dijelova (a)+(b)+(c)+(d)+(e)=100; pri čemu je jedan od dva ili više farmaceutskih razrjeđivača mikrokristalna celuloza pri čemu mikrokristalna celuloza čini od 7 do 30 mas.% dva ili više farmaceutskih razrjeđivača (b); i pri čemu je Sredstvo N-(2-{2-dimetilaminoetil-metilamino}-4-metoksi-5-{[4-(1-metilindol-3-il)pirimidin-2-il]amino}fenil)prop-2-enamid ili njegova farmaceutski prihvatljiva sol.
2. Farmaceutski pripravak prema zahtjevu 1 naznačen time što farmaceutski pripravak sadrži od 1 do 2,5 dijela jednog ili više farmaceutskih sredstava za povećanje skliskosti (e).
3. Farmaceutski pripravak prema zahtjevu 1 ili zahtjevu 2 naznačen time što jedno ili više farmaceutskih sredstava za povećanje skliskosti (e) sadrži natrijev stearil fumarat i/ili jedan ili više behenatnih estera glicerina.
4. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 3, naznačen time što farmaceutski pripravak sadrži od 2 do 10 dijelova jednog ili više farmaceutskih sredstava za raspadanje (c).
5. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 4 naznačen time što jedno ili više farmaceutskih sredstava za raspadanje (c) sadrži nisko supstituiranu hidroksipropil celulozu.
6. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 5, naznačen time što farmaceutski pripravak sadrži od 0 do 0,25 dijelova jednog ili više farmaceutskih sredstava za topivost (d).
7. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 6, naznačen time što farmaceutsko sredstvo za topivost (d) nije prisutno.
8. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time što farmaceutski pripravak sadrži od 5 do 50 dijelova Sredstva (a).
9. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time što farmaceutski pripravak sadrži od 7 do 30 dijelova Sredstva (a).
10. Farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 9 naznačen time što je Sredstvo mezilatna sol N-(2-{2-dimetilaminoetil-metilamino}-4-metoksi-5-{[4-(1-metilindol-3-il)pirimidin-2-il]amino}fenil)prop-2-enamida.
11. Farmaceutski pripravak prema zahtjevu 1 naznačen time što sadrži: (a) od 5 do 50 dijelova Sredstva; (b) od 5 do 96 dijelova dva ili više farmaceutskih razrjeđivača; (c) od 2 do 15 dijelova jednog ili više farmaceutskih sredstava za raspadanje; (d) od 0 do 0,75 dijelova jednog ili više farmaceutskih sredstava za topivost; i (e) od 0,5 do 3 dijela jednog ili više farmaceutskih sredstava za povećanje skliskosti; pri čemu svi dijelovi su maseni i zbroj dijelova (a)+(b)+(c)+(d)+(e)=100; pri čemu je jedan od dva ili više farmaceutskih razrjeđivača mikrokristalna celuloza pri čemu mikrokristalna celuloza čini od 7 do 30 mas.% dva ili više farmaceutskih razrjeđivača (b) i pri čemu osim mikrokristalne celuloze, drugi farmaceutski razrjeđivač(i) unutar dva ili više farmaceutskih razrjeđivača je/su odabrani od celuloznog acetata, eritritola, etilceluloze, fruktoze, inulina, izomalta, laktitola, laktoze, maltitola, maltodekstrina, maltoze, manitola, polidekstroze, polietilen glikola, pululana, simetikona, natrijevog klorida, sorbitola, škroba, saharoze, trehaloze i ksilitola; i pri čemu jedno ili više farmaceutskih sredstava za raspadanje (c) sadrži nisko supstituiranu hidroksipropil celulozu i pri čemu jedno ili više farmaceutskih sredstava za povećanje skliskosti (e) sadrži natrijev stearil fumarat i/ili jedan ili više behenatnih estera glicerina; i pri čemu je Sredstvo mezilatna sol N-(2-{2-dimetilaminoetil-metilamino}-4-metoksi-5-{[4-(1-metilindol-3-il)pirimidin-2-il]amino}fenil)prop-2-enamida.
12. Farmaceutski pripravak prema zahtjevu 1, naznačen time što je farmaceutski pripravak jezgra tablete koja se sastoji od: (i) 19,07 mas.% mezilatne soli N-(2-{2-dimetilaminoetil-metilamino}-4-metoksi-5-{[4-(1-metilindol-3-il)pirimidin-2-il]amino}fenil)prop-2-enamida; (ii) 58,93 mas.% manitola; (iii) 15,00 mas.% mikrokristalne celuloze; (iv) 5,000 mas.% nisko supstituirane hidroksipropil celuloze; i (v) 2,00 mas.% natrijevog stearil fumarata.
13. Farmaceutski pripravak, prema bilo kojem od patentnih zahtjeva 1 do 12, naznačen time što je za uporabu kao lijek.
14. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 13, naznačen time što je uporaba za liječenje karcinoma.
15. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 14, naznačen time što rak je rak pluća ne-malih stanica
16. Farmaceutska tableta, naznačena time što sadrži farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 12.
17. Farmaceutska tableta koja sadrži jezgru tablete, pri čemu jezgra tablete sadrži farmaceutski pripravak prema bilo kojem od patentnih zahtjeva 1 do 12, naznačena time što jezgra tablete ima premaz.
18. Farmaceutska tableta prema zahtjevu 16 ili zahtjevu 17, naznačena time što se koristi u liječenju karcinoma.
HRP20210749TT 2014-01-02 2021-05-12 Farmaceutski pripravci koji sadrže azd9291 HRP20210749T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1400034.3A GB201400034D0 (en) 2014-01-02 2014-01-02 Pharmaceutical Compositions comprising AZD9291
EP15700082.9A EP3089741B1 (en) 2014-01-02 2015-01-02 Pharmaceutical compositions comprising azd9291
PCT/GB2015/050001 WO2015101791A1 (en) 2014-01-02 2015-01-02 Pharmaceutical compositions comprising azd9291

Publications (1)

Publication Number Publication Date
HRP20210749T1 true HRP20210749T1 (hr) 2021-06-25

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HRP20210749TT HRP20210749T1 (hr) 2014-01-02 2021-05-12 Farmaceutski pripravci koji sadrže azd9291

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US (4) US10183020B2 (hr)
EP (1) EP3089741B1 (hr)
JP (1) JP6588915B2 (hr)
KR (1) KR102336378B1 (hr)
CN (2) CN114712362A (hr)
AR (1) AR098989A1 (hr)
AU (1) AU2015204218B2 (hr)
CA (1) CA2933403C (hr)
CL (1) CL2016001609A1 (hr)
CR (1) CR20160310A (hr)
CY (1) CY1124848T1 (hr)
DK (1) DK3089741T3 (hr)
DO (1) DOP2016000156A (hr)
EA (1) EA034243B9 (hr)
ES (1) ES2873226T3 (hr)
GB (1) GB201400034D0 (hr)
GT (1) GT201600142A (hr)
HK (1) HK1225655A1 (hr)
HR (1) HRP20210749T1 (hr)
HU (1) HUE054344T2 (hr)
IL (1) IL246186B (hr)
LT (1) LT3089741T (hr)
MX (1) MX367358B (hr)
MY (1) MY183536A (hr)
NI (1) NI201600098A (hr)
NZ (1) NZ721298A (hr)
PE (1) PE20161170A1 (hr)
PH (1) PH12016501310A1 (hr)
PL (1) PL3089741T3 (hr)
PT (1) PT3089741T (hr)
RS (1) RS61927B1 (hr)
SG (1) SG11201605339QA (hr)
SI (1) SI3089741T1 (hr)
TW (1) TWI702953B (hr)
UY (1) UY35933A (hr)
WO (1) WO2015101791A1 (hr)
ZA (1) ZA201605300B (hr)

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CA2933403C (en) 2022-03-29
DK3089741T3 (da) 2021-06-07
CL2016001609A1 (es) 2016-12-09
CY1124848T1 (el) 2022-11-25
NI201600098A (es) 2016-12-20
TWI702953B (zh) 2020-09-01
CN105848647B (zh) 2022-04-26
JP6588915B2 (ja) 2019-10-09
ZA201605300B (en) 2022-10-26
US20190111057A1 (en) 2019-04-18
US20200360378A1 (en) 2020-11-19
CN105848647A (zh) 2016-08-10
GT201600142A (es) 2019-08-12
CA2933403A1 (en) 2015-07-09
DOP2016000156A (es) 2016-08-15
PE20161170A1 (es) 2016-11-24
EA034243B1 (ru) 2020-01-21
PT3089741T (pt) 2021-06-11
MX367358B (es) 2019-08-16
KR20160101720A (ko) 2016-08-25
IL246186A0 (en) 2016-07-31
CR20160310A (es) 2016-09-23
GB201400034D0 (en) 2014-02-19
LT3089741T (lt) 2021-06-10
US20160324854A1 (en) 2016-11-10
AU2015204218B2 (en) 2017-06-15
SI3089741T1 (sl) 2021-08-31
MX2016008744A (es) 2016-09-08
EA034243B9 (ru) 2020-04-10
WO2015101791A1 (en) 2015-07-09
EP3089741A1 (en) 2016-11-09
PH12016501310A1 (en) 2016-09-14
KR102336378B1 (ko) 2021-12-08
CN114712362A (zh) 2022-07-08
US20220395502A1 (en) 2022-12-15
HUE054344T2 (hu) 2021-08-30
ES2873226T3 (es) 2021-11-03
EP3089741B1 (en) 2021-03-10
NZ721298A (en) 2017-10-27
JP2017501201A (ja) 2017-01-12
AU2015204218A1 (en) 2016-07-07
US10183020B2 (en) 2019-01-22
EA201691242A1 (ru) 2016-12-30
IL246186B (en) 2020-07-30
UY35933A (es) 2015-07-31
PL3089741T3 (pl) 2021-09-27
SG11201605339QA (en) 2016-07-28
MY183536A (en) 2021-02-25
AR098989A1 (es) 2016-06-22
HK1225655A1 (zh) 2017-09-15
TW201609101A (zh) 2016-03-16
RS61927B1 (sr) 2021-06-30

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