HRP20231613T1 - Pripravci koji sadrže sredstvo za unošenje i njihova priprava - Google Patents
Pripravci koji sadrže sredstvo za unošenje i njihova priprava Download PDFInfo
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- HRP20231613T1 HRP20231613T1 HRP20231613TT HRP20231613T HRP20231613T1 HR P20231613 T1 HRP20231613 T1 HR P20231613T1 HR P20231613T T HRP20231613T T HR P20231613TT HR P20231613 T HRP20231613 T HR P20231613T HR P20231613 T1 HRP20231613 T1 HR P20231613T1
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- Croatia
- Prior art keywords
- preparation according
- pharmaceutical preparation
- glp
- pharmaceutical
- lubricant
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- 238000002360 preparation method Methods 0.000 title claims 12
- 229940124447 delivery agent Drugs 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 13
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims 6
- 239000008187 granular material Substances 0.000 claims 5
- 239000000314 lubricant Substances 0.000 claims 5
- 108090000765 processed proteins & peptides Proteins 0.000 claims 5
- 101710198884 GATA-type zinc finger protein 1 Proteins 0.000 claims 4
- 102400000322 Glucagon-like peptide 1 Human genes 0.000 claims 4
- DTHNMHAUYICORS-KTKZVXAJSA-N Glucagon-like peptide 1 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 DTHNMHAUYICORS-KTKZVXAJSA-N 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 claims 3
- 229960002446 octanoic acid Drugs 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 238000007908 dry granulation Methods 0.000 claims 2
- 238000005469 granulation Methods 0.000 claims 2
- 230000003179 granulation Effects 0.000 claims 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical group [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims 2
- 102000009027 Albumins Human genes 0.000 claims 1
- 108010088751 Albumins Proteins 0.000 claims 1
- 102400000324 Glucagon-like peptide 1(7-37) Human genes 0.000 claims 1
- 101800004266 Glucagon-like peptide 1(7-37) Proteins 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- DLSWIYLPEUIQAV-UHFFFAOYSA-N Semaglutide Chemical compound CCC(C)C(NC(=O)C(Cc1ccccc1)NC(=O)C(CCC(O)=O)NC(=O)C(CCCCNC(=O)COCCOCCNC(=O)COCCOCCNC(=O)CCC(NC(=O)CCCCCCCCCCCCCCCCC(O)=O)C(O)=O)NC(=O)C(C)NC(=O)C(C)NC(=O)C(CCC(N)=O)NC(=O)CNC(=O)C(CCC(O)=O)NC(=O)C(CC(C)C)NC(=O)C(Cc1ccc(O)cc1)NC(=O)C(CO)NC(=O)C(CO)NC(=O)C(NC(=O)C(CC(O)=O)NC(=O)C(CO)NC(=O)C(NC(=O)C(Cc1ccccc1)NC(=O)C(NC(=O)CNC(=O)C(CCC(O)=O)NC(=O)C(C)(C)NC(=O)C(N)Cc1cnc[nH]1)C(C)O)C(C)O)C(C)C)C(=O)NC(C)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CCCNC(N)=N)C(=O)NCC(O)=O DLSWIYLPEUIQAV-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 239000002775 capsule Substances 0.000 claims 1
- 238000007906 compression Methods 0.000 claims 1
- 230000006835 compression Effects 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 235000019359 magnesium stearate Nutrition 0.000 claims 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims 1
- 239000008108 microcrystalline cellulose Substances 0.000 claims 1
- 229940016286 microcrystalline cellulose Drugs 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 1
- 229940069328 povidone Drugs 0.000 claims 1
- 229950011186 semaglutide Drugs 0.000 claims 1
- 108010060325 semaglutide Proteins 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000007909 solid dosage form Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/26—Glucagons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/60—Salicylic acid; Derivatives thereof
- A61K31/609—Amides, e.g. salicylamide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Endocrinology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Organic Chemistry (AREA)
- Obesity (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Claims (17)
1. Pripravak koji sadrži granulu koja sadrži sol N-(8-(2-hidroksibenzoil)amino)kaprilne kiseline i mazivo, naznačen time što se navedenu granulu proizvodi suhim granuliranjem, te dobiva miješanjem navedene soli N-(8-(2-hidroksibenzoil)amino)kaprilne kiseline s navedenim mazivom u trajanju od više od 5 minuta prije suhog granuliranja, što je količina navedenog maziva najmanje 2% (tež./tež.) od navedene granule, što pripravak sadrži jedan ili više intragranularnih dijelova i ekstragranularni dio, što su jedan ili više intragranularnih dijelova granulirani, te što se ekstragranularni dio doda nakon granuliranja.
2. Pripravak u skladu s patentnim zahtjevom 1, naznačen time što navedeno miješanje traje 10, 20 ili 30 minuta.
3. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što navedeno miješanje traje najmanje 30 minuta ili najmanje 40 minuta, primjerice najmanje 50 minuta.
4. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što je količina navedenog maziva najviše 10 % (tež./tež.), primjerice najviše 8, 7 ili 6 % (tež./tež.), od navedene granule.
5. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što je mazivo magnezijev stearat.
6. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što navedeno miješanje traje najviše 12 sata, primjerice najviše 10, 8, 6, 4 ili 2 sata.
7. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što navedene granule se proizvodi komprimiranjem valjcima.
8. Pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što je navedena sol N-(8-(2-hidroksibenzoil)amino)kaprilne kiseline natrijev N-(8-(2-hidroksibenzoil)amino)kaprilat (SNAC).
9. Farmaceutski pripravak comprising a pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačen time što pripravak sadrži jedan ili više intragranularnih dijelova i ekstragranularni dio, što su jedan ili više intragranularnih dijelova granulirani, te što se ekstragranularni dio doda nakon granuliranja.
10. Farmaceutski pripravak u skladu s patentnim zahtjevom 9, naznačen time što farmaceutski pripravak dodatno sadrži farmaceutski aktivni sastojak, poput peptida GLP-1.
11. Farmaceutski pripravak u skladu s patentnim zahtjevom 10, naznačen time što navedeni peptid GLP-1 sadrži skupinu kojem se veže na albumin.
12. Farmaceutski pripravak u skladu s patentnim zahtjevom 10, naznačen time što navedeni peptid GLP-1 sadrži supstituent, kovalentno vezan na peptid, poput masne kiseline ili masne dikiseline.
13. Farmaceutski pripravak u skladu s patentnim zahtjevom 10, naznačen time što je navedeni peptid GLP-1 semaglutid, poznat i kao Nε26-[2-(2-{2-[2-(2-{2-[(S)-4-karboksi-4-(17-karboksiheptadekanoilamino)butirilamino]etoksi}etoksi)acetilamino]etoksi}etoksi)acetil][Aib8,Arg34]GLP-1(7-37).
14. Farmaceutski pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva 9-13, naznačen time što navedeni farmaceutski pripravak dodatno sadrži jedno ili više farmaceutski prihvatljivih pomoćnih sredstava, poput jednog ili više sastojaka, koje se bira iz skupine koju čine punilo, poput mikrokristalne celuloze, te veziva, poput povidona.
15. Farmaceutski pripravak u skladu s bilo kojim od prethodnih patentnih zahtjeva 9-14, naznačen time što je navedeni farmaceutski pripravak u obliku čvrstog oblika doziranja, poput tablete, kapsule ili vrećice.
16. Farmaceutski pripravak u skladu s patentnim zahtjevom 15, naznačen time što navedeni farmaceutski pripravak treba primijeniti oralno/oralnom primjenom.
17. Farmaceutski pripravak u skladu s bilo kojim od patentnih zahtjeva 9-16, naznačen time što je namijenjen upotrebi u medicini, primjerice u liječenju dijabetesa ili pretilosti.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12160742 | 2012-03-22 | ||
US201361748844P | 2013-01-04 | 2013-01-04 | |
EP13153422 | 2013-01-31 | ||
EP18212576.5A EP3542790B1 (en) | 2012-03-22 | 2013-03-15 | Compositions comprising a delivery agent and preparation thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20231613T1 true HRP20231613T1 (hr) | 2024-03-15 |
Family
ID=49221869
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HRP20231613TT HRP20231613T1 (hr) | 2012-03-22 | 2013-03-15 | Pripravci koji sadrže sredstvo za unošenje i njihova priprava |
Country Status (11)
Country | Link |
---|---|
US (1) | US10335369B2 (hr) |
EP (3) | EP3542790B1 (hr) |
JP (1) | JP6356660B2 (hr) |
CN (3) | CN111494323B (hr) |
ES (1) | ES2965469T3 (hr) |
HR (1) | HRP20231613T1 (hr) |
HU (1) | HUE064694T2 (hr) |
PL (2) | PL2827845T3 (hr) |
RS (2) | RS64942B1 (hr) |
SI (1) | SI2827845T1 (hr) |
WO (1) | WO2013139695A1 (hr) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2600440C3 (ru) | 2010-12-16 | 2021-12-10 | Ново Нордиск А/С | Твердые композиции, содержащие агонист glp-1 и соль n-(8-(2-гидроксибензоил)амино)каприловой кислоты |
WO2012140117A1 (en) | 2011-04-12 | 2012-10-18 | Novo Nordisk A/S | Double-acylated glp-1 derivatives |
ES2952874T3 (es) | 2012-03-22 | 2023-11-06 | Novo Nordisk As | Composiciones de péptidos GLP-1 y preparación de estas |
RS64942B1 (sr) | 2012-03-22 | 2024-01-31 | Novo Nordisk As | Kompozicije koje obuhvataju sredstvo za isporuku i njihova priprema |
DK2827845T3 (en) | 2012-03-22 | 2019-04-01 | Novo Nordisk As | COMPOSITIONS INCLUDING A PROCEDURE AND PREPARING THEREOF |
CN104487056A (zh) | 2012-06-20 | 2015-04-01 | 诺和诺德A/S(股份有限公司) | 包含肽和递送剂的片剂制剂 |
KR20180115814A (ko) | 2013-05-02 | 2018-10-23 | 노보 노르디스크 에이/에스 | Glp-1 화합물의 경구 투여 |
CN104173313B (zh) * | 2014-08-25 | 2017-05-17 | 杭州朱养心药业有限公司 | 利伐沙班片剂药物组合物 |
CA2973099C (en) | 2015-01-12 | 2021-09-14 | Enteris Biopharma, Inc. | Solid oral dosage forms |
WO2018121702A1 (zh) * | 2016-12-30 | 2018-07-05 | 江苏恒瑞医药股份有限公司 | 一种glp-1类似物的药物组合物及其制备方法 |
TWI797133B (zh) | 2017-06-09 | 2023-04-01 | 丹麥商諾佛 儂迪克股份有限公司 | 用於經口投予的固體組成物 |
MA53076B1 (fr) * | 2018-02-02 | 2023-11-30 | Novo Nordisk As | Compositions solides comportant un agoniste glp-1, du sel d'acide n-(8-(2-hydroxybenzoyl)amino)caprylate et un lubrifiant |
TWI829687B (zh) * | 2018-05-07 | 2024-01-21 | 丹麥商諾佛 儂迪克股份有限公司 | 包含glp-1促效劑與n-(8-(2-羥基苯甲醯基)胺基)辛酸之鹽的固體組成物 |
CN113329810A (zh) * | 2019-01-24 | 2021-08-31 | 诺和诺德股份有限公司 | 辊压机和使用辊压机的干法制粒方法 |
WO2021023855A1 (en) * | 2019-08-07 | 2021-02-11 | Novo Nordisk A/S | Solid compositions comprising an egf(a) derivative and a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid |
CN114340655A (zh) | 2019-09-02 | 2022-04-12 | 诺和诺德股份有限公司 | 生产包含glp-1肽的片剂的方法 |
WO2021043971A1 (en) | 2019-09-06 | 2021-03-11 | Novo Nordisk A/S | Method and equipment for fractionation of granules for use in pharmaceutical compositions |
JP2023502004A (ja) | 2019-11-07 | 2023-01-20 | ノヴォ ノルディスク アー/エス | Glp-1作動薬、sglt2阻害剤、およびn-(8-(2-ヒドロキシベンゾイル)アミノ)カプリル酸の塩を含む固形組成物 |
JP2023524695A (ja) * | 2020-04-29 | 2023-06-13 | ノヴォ ノルディスク アー/エス | Glp-1作動薬およびヒスチジンを含む固形組成物 |
CN111517980B (zh) * | 2020-05-14 | 2021-02-09 | 台州浦凯医药科技有限公司 | N-[8-(2-羟基苯甲酰基)氨基]辛酸一钾晶型化合物、制备方法及用途 |
BR112023000270A2 (pt) | 2020-07-22 | 2023-01-31 | Novo Nordisk As | Composto, composição farmacêutica, e, peptídeo |
CN116157414A (zh) * | 2020-07-22 | 2023-05-23 | 诺和诺德股份有限公司 | Glp-1和gip受体共激动剂 |
CN113117050B (zh) * | 2021-05-06 | 2022-04-26 | 合肥天汇孵化科技有限公司 | 多肽组合物及其用途 |
IL308280A (en) | 2021-05-07 | 2024-01-01 | Lilly Co Eli | Tablet worn out |
WO2023285580A1 (en) | 2021-07-15 | 2023-01-19 | Novo Nordisk A/S | Tablet comprising a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid |
CA3239474A1 (en) * | 2021-12-01 | 2023-06-08 | Hua He | Pharmaceutical composition of glp-1 and gip receptor dual agonist and use thereof |
TW202330584A (zh) | 2022-01-20 | 2023-08-01 | 丹麥商諾佛 儂迪克股份有限公司 | 前藥及其用途 |
CN114984191B (zh) * | 2022-07-04 | 2022-10-25 | 北京惠之衡生物科技有限公司 | 一种多肽类药物口服递送组合物 |
WO2024110614A1 (en) | 2022-11-25 | 2024-05-30 | Novo Nordisk A/S | Oral administration of peptide therapeutics, such as glp-1 |
Family Cites Families (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PH24180A (en) | 1986-03-12 | 1990-03-22 | Glaxo Group Ltd | Macrolide compounds,pharmaceutical composition containing said compound and method of use thereof |
DK39892D0 (da) | 1992-03-25 | 1992-03-25 | Bernard Thorens | Peptid |
US5869602A (en) | 1995-03-17 | 1999-02-09 | Novo Nordisk A/S | Peptide derivatives |
US5650386A (en) | 1995-03-31 | 1997-07-22 | Emisphere Technologies, Inc. | Compositions for oral delivery of active agents |
US5866536A (en) | 1995-03-31 | 1999-02-02 | Emisphere Technologies, Inc. | Compounds and compositions for delivering active agents |
SE9600070D0 (sv) | 1996-01-08 | 1996-01-08 | Astra Ab | New oral pharmaceutical dosage forms |
DE69737479D1 (de) | 1996-08-30 | 2007-04-26 | Novo Nordisk As | Glp-1 derivate |
US5773647A (en) | 1997-02-07 | 1998-06-30 | Emisphere Technologies, Inc. | Compounds and compositions for delivering active agents |
EP1056775B1 (en) | 1998-02-27 | 2010-04-28 | Novo Nordisk A/S | Glp-1 derivatives of glp-1 and exendin with protracted profile of action |
JP2002504518A (ja) | 1998-02-27 | 2002-02-12 | ノボ ノルディスク アクティーゼルスカブ | 部分的に構造化されたミセルー様凝集体を形成する、25%を超えるヘリックス−含有率を有するglp−1誘導体 |
WO1999043707A1 (en) | 1998-02-27 | 1999-09-02 | Novo Nordisk A/S | N-terminally modified glp-1 derivatives |
DE69942306D1 (de) | 1998-02-27 | 2010-06-10 | Novo Nordisk As | Abkömmlinge von glp-1 analogen |
SE9802080D0 (sv) | 1998-06-11 | 1998-06-11 | Hellstroem | Pharmaceutical composition for the treatment of functional dyspepsia and/or irritable bowel syndrome and new use of substances therein |
DE60023841T2 (de) | 1999-02-05 | 2006-05-24 | Emisphere Technologies, Inc. | Verfahren zur herstellung alkylierter salicylamide |
CA2363123C (en) | 1999-02-22 | 2011-09-06 | Kenneth Iain Cumming | Solid oral dosage form containing an enhancer |
US7658938B2 (en) | 1999-02-22 | 2010-02-09 | Merrion Reasearch III Limited | Solid oral dosage form containing an enhancer |
AU3240900A (en) | 1999-02-22 | 2000-09-04 | Emisphere Holdings, Inc. | Solid oral dosage form containing heparin or a heparinoid in combination with a carrier |
GB9923436D0 (en) | 1999-10-04 | 1999-12-08 | American Home Prod | Pharmaceutical compositions |
US6793934B1 (en) | 1999-12-08 | 2004-09-21 | Shire Laboratories, Inc. | Solid oral dosage form |
AU2001275231A1 (en) | 2000-06-02 | 2001-12-11 | Emisphere Technologies, Inc. | Method of preparing salicylamides |
US7049283B2 (en) | 2000-12-06 | 2006-05-23 | Novartis Ag | Pharmaceutical compositions for the oral delivery of pharmacologically active agents |
US20030068356A1 (en) | 2001-07-10 | 2003-04-10 | Pather S. Indiran | Sequential drug delivery systems |
JP5196701B2 (ja) | 2001-11-29 | 2013-05-15 | エミスフィアー テクノロジーズ インコーポレイテッド | クロモリンナトリウムの経口投与用製剤 |
KR100676025B1 (ko) | 2002-02-01 | 2007-01-29 | 화이자 프로덕츠 인코포레이티드 | 아지쓰로마이신의 건조 과립화 제제 |
WO2003072195A2 (en) | 2002-02-20 | 2003-09-04 | Eli Lilly And Company | Method for administering glp-1 molecules |
JP2004131398A (ja) * | 2002-10-08 | 2004-04-30 | Taihei Chemical Industrial Co Ltd | 錠剤用滑沢剤 |
EP1624882A2 (en) | 2003-05-14 | 2006-02-15 | Emisphere Technologies, Inc. | Compositions for delivering peptide yy and pyy agonists |
JP5032844B2 (ja) | 2003-07-11 | 2012-09-26 | ノバルティス アーゲー | 微粉末形態の送達物質を含む経口投与用医薬組成物 |
BRPI0414539B8 (pt) | 2003-09-19 | 2021-05-25 | Novo Nordisk As | composto, composição farmacêutica, e, uso de um composto |
KR20060109940A (ko) | 2003-12-18 | 2006-10-23 | 노보 노르디스크 에이/에스 | 알부민-유사제에 연결된 신규 glp-1 유사체 |
ATE461217T1 (de) | 2003-12-18 | 2010-04-15 | Novo Nordisk As | Glp-1-verbindungen |
US20060286129A1 (en) | 2003-12-19 | 2006-12-21 | Emisphere Technologies, Inc. | Oral GLP-1 formulations |
WO2005099672A1 (en) | 2004-04-13 | 2005-10-27 | Ranbaxy Laboratories Limited | A modified release pharmaceutical formulation comprising amoxicillin and clavulanate |
MXPA06012841A (es) * | 2004-05-06 | 2007-02-15 | Emisphere Tech Inc | Forma de dosificacion solida de heparina humeda. |
JP5254610B2 (ja) | 2004-05-14 | 2013-08-07 | エミスフェアー・テクノロジーズ・インク | 活性薬剤を送達するための化合物および組成物 |
CN101010339B (zh) | 2004-07-02 | 2011-11-09 | 布里斯托尔-迈尔斯斯奎布公司 | 人类胰高血糖素样肽-1调节剂及它们在治疗糖尿病及相关病况中的用途 |
EP2289560B1 (en) | 2004-07-08 | 2015-04-22 | Novo Nordisk A/S | Polypeptide protracting tags comprising a tetrazole moiety |
US20060078622A1 (en) * | 2004-08-13 | 2006-04-13 | Emisphere Technologies, Inc. | Pharmaceutical formulations containing microparticles or nanoparticles of a delivery agent |
WO2006037810A2 (en) | 2004-10-07 | 2006-04-13 | Novo Nordisk A/S | Protracted glp-1 compounds |
US8030273B2 (en) | 2004-10-07 | 2011-10-04 | Novo Nordisk A/S | Protracted exendin-4 compounds |
JP5175553B2 (ja) * | 2005-02-01 | 2013-04-03 | エミスフェアー・テクノロジーズ・インク | 胃内滞留および制御放出型送達系 |
TWI372629B (en) | 2005-03-18 | 2012-09-21 | Novo Nordisk As | Acylated glp-1 compounds |
BRPI0608516A2 (pt) | 2005-03-18 | 2010-11-16 | Novo Nordisk As | análogo de glp-1, método para aumentar o tempo de ação em um paciente de um análogo de glp-1, composição farmacêutica, e, uso de um composto |
US20080260818A1 (en) | 2005-03-28 | 2008-10-23 | Dexcel Pharma Technologies Ltd. | Controlled Absorption of Statins in the Intestine |
US20070049557A1 (en) | 2005-08-24 | 2007-03-01 | Hashim Ahmed | Solid pharmaceutical dosage forms comprising bisphosphonates and modified amino acid carriers |
AU2006318815B2 (en) | 2005-11-17 | 2010-08-19 | Novartis Ag | Pharmaceutical composition |
WO2007117706A2 (en) | 2006-04-07 | 2007-10-18 | Merrion Research Iii Limited | Solid oral dosage form containing an enhancer |
US8927015B2 (en) | 2006-04-12 | 2015-01-06 | Emisphere Technologies, Inc. | Formulations for delivering insulin |
JP2009539862A (ja) | 2006-06-09 | 2009-11-19 | メリオン リサーチ Iii リミテッド | 強化剤を含む固体経口投与剤形 |
CA2656019C (en) * | 2006-06-28 | 2016-09-13 | Emisphere Technologies, Inc. | Gallium nitrate formulations |
ES2296529B1 (es) | 2006-08-07 | 2009-04-01 | Laboratorios Farmaceuticos Rovi, S.A. | Composicion farmaceutica con promotores de absorcion. |
EP2057189B1 (en) | 2006-08-25 | 2013-03-06 | Novo Nordisk A/S | Acylated exendin-4 compounds |
CA2662080C (en) | 2006-09-07 | 2012-07-17 | F. Hoffmann-La Roche Ag | A process for the manufacture of snac (salcaprozate sodium) |
WO2008039351A2 (en) | 2006-09-22 | 2008-04-03 | Novartis Ag | Method of manufacturing tablets containing pharmacologically active agents |
WO2008070547A1 (en) * | 2006-12-01 | 2008-06-12 | Emisphere Technologies Inc. | Improved acyclovir formulations |
MX2009009243A (es) | 2007-03-02 | 2009-09-08 | Novartis Ag | Administracion oral de una calcitonina. |
WO2009032749A2 (en) | 2007-08-29 | 2009-03-12 | The Regents Of The University Of Californina | Salicylanilide modified peptides for use as oral therapeutics |
CN101868476B (zh) | 2007-09-05 | 2015-02-25 | 诺沃-诺迪斯克有限公司 | 胰高血糖素样肽-1衍生物及其制药用途 |
WO2009030771A1 (en) | 2007-09-05 | 2009-03-12 | Novo Nordisk A/S | Peptides derivatized with a-b-c-d- and their therapeutical use |
JP2010538049A (ja) | 2007-09-05 | 2010-12-09 | ノボ・ノルデイスク・エー/エス | 切断型glp−1誘導体及びその治療的使用 |
NZ585135A (en) | 2007-10-16 | 2012-08-31 | Biocon Ltd | An orally administerable solid pharmaceutical composition comprising in-105 and a process thereof |
ES2443817T3 (es) | 2007-11-02 | 2014-02-20 | Emisphere Technologies, Inc. | Método para tratar la deficiencia de vitamina B12 |
US20090124639A1 (en) * | 2007-11-06 | 2009-05-14 | Emisphere Technologies Inc. | valacyclovir formulations |
US20100317057A1 (en) | 2007-12-28 | 2010-12-16 | Novo Nordisk A/S | Semi-recombinant preparation of glp-1 analogues |
EP2331072B8 (en) * | 2008-08-18 | 2020-08-26 | Entera Bio Ltd. | Methods and compositions for oral administration of proteins |
KR20160143897A (ko) * | 2009-02-13 | 2016-12-14 | 베링거 인겔하임 인터내셔날 게엠베하 | Dpp-4 억제제(리나글립틴)을 임의로 다른 당뇨병 치료제와 병용하여 포함하는 당뇨병 치료 약제 |
CA2784120A1 (en) | 2009-12-16 | 2011-07-14 | Nod Pharmaceuticals, Inc. | Compositions and methods for oral drug delivery |
US20110182985A1 (en) | 2010-01-28 | 2011-07-28 | Coughlan David C | Solid Pharmaceutical Composition with Enhancers and Methods of Preparing thereof |
WO2011109787A1 (en) | 2010-03-05 | 2011-09-09 | Conjuchem, Llc | Methods of administering insulinotropic peptides |
WO2011116139A2 (en) | 2010-03-16 | 2011-09-22 | Chiasma Inc. | Improved pharmaceutical compositions and methods of delivery |
EA033415B1 (ru) | 2010-05-05 | 2019-10-31 | Boehringer Ingelheim Int | Способы лечения ожирения, применение ингибитора dpp-4 в этих способах и способ лечения пациентов, страдающих диабетом типа 2 |
DE202010015867U1 (de) | 2010-11-25 | 2011-05-05 | Buchhalter, Thomas | Elektromechanische Halterung zur Aufnahme von Navigations- und Kommunikationsgeräte im KFZ |
RU2600440C3 (ru) | 2010-12-16 | 2021-12-10 | Ново Нордиск А/С | Твердые композиции, содержащие агонист glp-1 и соль n-(8-(2-гидроксибензоил)амино)каприловой кислоты |
RS64942B1 (sr) | 2012-03-22 | 2024-01-31 | Novo Nordisk As | Kompozicije koje obuhvataju sredstvo za isporuku i njihova priprema |
ES2952874T3 (es) | 2012-03-22 | 2023-11-06 | Novo Nordisk As | Composiciones de péptidos GLP-1 y preparación de estas |
CN104487056A (zh) | 2012-06-20 | 2015-04-01 | 诺和诺德A/S(股份有限公司) | 包含肽和递送剂的片剂制剂 |
KR20180115814A (ko) | 2013-05-02 | 2018-10-23 | 노보 노르디스크 에이/에스 | Glp-1 화합물의 경구 투여 |
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RS58636B1 (sr) | 2019-05-31 |
JP6356660B2 (ja) | 2018-07-11 |
EP4331667A2 (en) | 2024-03-06 |
CN111494323A (zh) | 2020-08-07 |
CN104203221A (zh) | 2014-12-10 |
PL2827845T3 (pl) | 2019-06-28 |
ES2965469T3 (es) | 2024-04-15 |
EP4331667A3 (en) | 2024-05-08 |
US20150031606A1 (en) | 2015-01-29 |
US10335369B2 (en) | 2019-07-02 |
CN111494323B (zh) | 2023-03-28 |
EP2827845A1 (en) | 2015-01-28 |
EP2827845B1 (en) | 2018-12-26 |
EP3542790A1 (en) | 2019-09-25 |
CN111494324A (zh) | 2020-08-07 |
CN111494324B (zh) | 2023-05-16 |
RS64942B1 (sr) | 2024-01-31 |
EP3542790C0 (en) | 2023-09-13 |
PL3542790T3 (pl) | 2024-02-26 |
WO2013139695A1 (en) | 2013-09-26 |
HUE064694T2 (hu) | 2024-04-28 |
EP3542790B1 (en) | 2023-09-13 |
SI2827845T1 (sl) | 2019-04-30 |
JP2015515459A (ja) | 2015-05-28 |
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