JPWO2019200274A5 - - Google Patents

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Publication number
JPWO2019200274A5
JPWO2019200274A5 JP2021505625A JP2021505625A JPWO2019200274A5 JP WO2019200274 A5 JPWO2019200274 A5 JP WO2019200274A5 JP 2021505625 A JP2021505625 A JP 2021505625A JP 2021505625 A JP2021505625 A JP 2021505625A JP WO2019200274 A5 JPWO2019200274 A5 JP WO2019200274A5
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JP
Japan
Prior art keywords
pharmaceutical composition
composition according
kda
item
hyaluronic acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2021505625A
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Japanese (ja)
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JP2021521280A (en
Publication date
Application filed filed Critical
Priority claimed from PCT/US2019/027257 external-priority patent/WO2019200274A1/en
Publication of JP2021521280A publication Critical patent/JP2021521280A/en
Publication of JPWO2019200274A5 publication Critical patent/JPWO2019200274A5/ja
Pending legal-status Critical Current

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Description

同等物
本発明の特定の実施形態を論じてきたが、上記の明細書は例示的なものであり、限定的なものではない。本発明の多くの変形は本明細書及び以下の特許請求の範囲を検討することにより、当業者に明らかになるのであろう。本発明の全範囲は、特許請求の範囲、それらの均等物の全範囲、及び明細書、並びにそのような変形を参照することによって決定されるべきである。

本発明は例えば以下の態様を含む。
[項1]
約50~約1000kDaの重量平均分子量(Mw)を有するヒアルロン酸又はその薬学的に許容される塩;及び
薬学的に許容される賦形剤
を含む医薬組成物。
[項2]
前記ヒアルロン酸が、約150kDaの重量平均分子量(Mw)を有する、項1に記載の医薬組成物。
[項3]
吸入に適した形態の、項1又は2に記載の医薬組成物。
[項4]
鼻腔内、肺内、気管内、気管支内、又は肺胞内投与に適した形態の、項1~3のいずれか1項に記載の医薬組成物。
[項5]
肺胞内投与に適した形態の、項4に記載の医薬組成物。
[項6]
乾燥粉末吸入器による投与に適した形態の、項1~5のいずれか1項に記載の医薬組成物。
[項7]
液体噴霧装置による投与に適した形態の、項1~5のいずれか1項に記載の医薬組成物。
[項8]
前記液体噴霧装置がエアロゾル装置である、項7に記載の医薬組成物。
[項9]
前記エアロゾル装置がネブライザー又は電気流体力学的エアロゾル装置である、項8に記載の医薬組成物。
[項10]
項1~6のいずれか1項に記載の医薬組成物を含む吸入器。
[項11]
約2μm~約3μmのサイズの液滴を送達するように構成された、項10に記載の吸入器。
[項12]
約50~約1000kDaの重量平均分子量(Mw)を有するヒアルロン酸又はその薬学的に許容される塩を対象に投与することを含む、対象における弾性線維関連障害を治療するための方法。
[項13]
前記ヒアルロン酸が、約150kDaの重量平均分子量(Mw)を有する、項12に記載の方法。
[項14]
吸入によってヒアルロン酸を投与することを含む、項12又は13に記載の方法。
[項15]
ヒアルロン酸を副鼻腔、肺系、気管、気管支、又は肺胞に投与することを含む、項12~14のいずれか1項に記載の方法。
[項16]
弾性線維関連障害が、皮膚弛緩症、ウィリアムス症候群、アルファ-1アンチトリプシン欠損症、肺気腫、慢性閉塞性肺疾患(COPD)、肝疾患、ブシュケ-オレンドルフ症候群、メンケス病、弾性線維性仮性黄色腫、マルファン症候群、ハーラー病、高血圧又は先天性心臓欠陥である、項12~15のいずれか1項に記載の方法。
[項17]
前記弾性線維関連障害がCOPDである、項16に記載の方法。
Equivalents Although specific embodiments of the present invention have been discussed, the above specification is exemplary and not limiting. Many variations of the invention will be apparent to those skilled in the art by examining the specification and the claims below. The entire scope of the invention should be determined by reference to the claims, the entire scope of their equivalents, and the specification, as well as such variations.

The present invention includes, for example, the following aspects.
[Item 1]
A pharmaceutical composition comprising hyaluronic acid or a pharmaceutically acceptable salt thereof having a weight average molecular weight (M w ) of about 50 to about 1000 kDa; and a pharmaceutically acceptable excipient.
[Item 2]
Item 2. The pharmaceutical composition according to Item 1, wherein the hyaluronic acid has a weight average molecular weight (M w ) of about 150 kDa.
[Item 3]
Item 2. The pharmaceutical composition according to Item 1 or 2, which is in a form suitable for inhalation.
[Item 4]
Item 6. The pharmaceutical composition according to any one of Items 1 to 3, which is in a form suitable for intranasal, intrapulmonary, tracheal, intrabronchial, or intraalveolar administration.
[Item 5]
Item 4. The pharmaceutical composition according to Item 4, which is in a form suitable for intra-alveolar administration.
[Item 6]
Item 6. The pharmaceutical composition according to any one of Items 1 to 5, which is in a form suitable for administration by a dry powder inhaler.
[Item 7]
Item 6. The pharmaceutical composition according to any one of Items 1 to 5, which is in a form suitable for administration by a liquid spray device.
[Item 8]
Item 6. The pharmaceutical composition according to Item 7, wherein the liquid spraying device is an aerosol device.
[Item 9]
Item 8. The pharmaceutical composition according to Item 8, wherein the aerosol device is a nebulizer or an electrohydrodynamic aerosol device.
[Item 10]
An inhaler containing the pharmaceutical composition according to any one of Items 1 to 6.
[Item 11]
Item 10. The inhaler according to Item 10, which is configured to deliver droplets having a size of about 2 μm to about 3 μm.
[Item 12]
A method for treating an elastic fiber-related disorder in a subject, comprising administering to the subject hyaluronic acid or a pharmaceutically acceptable salt thereof having a weight average molecular weight (M w ) of about 50 to about 1000 kDa.
[Item 13]
Item 12. The method according to Item 12, wherein the hyaluronic acid has a weight average molecular weight (M w ) of about 150 kDa.
[Item 14]
Item 12. The method according to Item 12 or 13, comprising administering hyaluronic acid by inhalation.
[Item 15]
12. The method of any one of Items 12-14, comprising administering hyaluronic acid to the sinuses, pulmonary system, trachea, bronchi, or alveoli.
[Item 16]
Elastic fiber-related disorders include cutis laxa, Williams syndrome, alpha-1 antitrypsin deficiency, emphysema, chronic obstructive pulmonary disease (COPD), liver disease, Buschke-Ollendorff syndrome, Menquez disease, elastic fibrous pseudoyellow tumor, The method according to any one of Items 12 to 15, which is Marfan syndrome, Harler's disease, hypertension or congenital heart defect.
[Item 17]
Item 16. The method according to Item 16, wherein the elastic fiber-related disorder is COPD.

Claims (18)

約50~約1000kDaの重量平均分子量(Mw)を有するヒアルロン酸又はその薬学的に許容される塩の、弾性線維関連障害を治療するための医薬の製造における使用。 Use of hyaluronic acid or a pharmaceutically acceptable salt thereof having a weight average molecular weight (M w ) of about 50 to about 1000 kDa in the manufacture of a pharmaceutical for treating elastic fiber-related disorders. 前記ヒアルロン酸が、約150kDaの重量平均分子量(Mw)を有する、請求項1に記載の使用 The use according to claim 1, wherein the hyaluronic acid has a weight average molecular weight (M w ) of about 150 kDa. 前記医薬は吸入によって投与される、請求項1又は2に記載の使用The use according to claim 1 or 2 , wherein the drug is administered by inhalation. 前記医薬は副鼻腔、肺系、気管、気管支、又は肺胞に投与される、請求項13のいずれか1項に記載の使用The use according to any one of claims 1 to 3 , wherein the drug is administered to the paranasal sinuses, pulmonary system, trachea, bronchi, or alveoli. 弾性線維関連障害が、皮膚弛緩症、ウィリアムス症候群、アルファ-1アンチトリプシン欠損症、肺気腫、慢性閉塞性肺疾患(COPD)、肝疾患、ブシュケ-オレンドルフ症候群、メンケス病、弾性線維性仮性黄色腫、マルファン症候群、ハーラー病、高血圧又は先天性心臓欠陥である、請求項14のいずれか1項に記載の使用Elastic fiber-related disorders include cutis laxa, Williams syndrome, alpha-1 antitrypsin deficiency, emphysema, chronic obstructive pulmonary disease (COPD), liver disease, Buschke-Ollendorff syndrome, Menquez disease, elastic fibrous pseudoyellow tumor, The use according to any one of claims 1 to 4 , which is Marfan syndrome, Harler's disease, hypertension or congenital heart defect. 前記弾性線維関連障害がCOPDである、請求項5に記載の使用The use according to claim 5 , wherein the elastic fiber-related disorder is COPD. 約50~約1000kDaの重量平均分子量(MWeight average molecular weight of about 50 to about 1000 kDa (M) ww )を有するヒアルロン酸又はその薬学的に許容される塩を含む、弾性線維関連障害を治療するための組成物。), A composition for treating elastic fiber-related disorders, comprising hyaluronic acid or a pharmaceutically acceptable salt thereof. 約50~約1000kDaの重量平均分子量(Mw)を有するヒアルロン酸又はその薬学的に許容される塩;及び
薬学的に許容される賦形剤
を含む医薬組成物。
A pharmaceutical composition comprising hyaluronic acid or a pharmaceutically acceptable salt thereof having a weight average molecular weight (M w ) of about 50 to about 1000 kDa; and a pharmaceutically acceptable excipient.
前記ヒアルロン酸が、約150kDaの重量平均分子量(Mw)を有する、請求項8に記載の医薬組成物。 The pharmaceutical composition according to claim 8 , wherein the hyaluronic acid has a weight average molecular weight (M w ) of about 150 kDa. 吸入に適した形態の、請求項8又は9に記載の医薬組成物。 The pharmaceutical composition according to claim 8 or 9 , which is in a form suitable for inhalation. 鼻腔内、肺内、気管内、気管支内、又は肺胞内投与に適した形態の、請求項810のいずれか1項に記載の医薬組成物。 The pharmaceutical composition according to any one of claims 8 to 10 , in a form suitable for intranasal, intrapulmonary, tracheal, intrabronchial, or intraalveolar administration. 肺胞内投与に適した形態の、請求項11に記載の医薬組成物。 The pharmaceutical composition according to claim 11 , which is in a form suitable for intra-alveolar administration. 乾燥粉末吸入器による投与に適した形態の、請求項812のいずれか1項に記載の医薬組成物。 The pharmaceutical composition according to any one of claims 8 to 12 , which is in a form suitable for administration by a dry powder inhaler. 液体噴霧装置による投与に適した形態の、請求項812のいずれか1項に記載の医薬組成物。 The pharmaceutical composition according to any one of claims 8 to 12 , which is in a form suitable for administration by a liquid spray device. 前記液体噴霧装置がエアロゾル装置である、請求項14に記載の医薬組成物。 The pharmaceutical composition according to claim 14 , wherein the liquid spraying device is an aerosol device. 前記エアロゾル装置がネブライザー又は電気流体力学的エアロゾル装置である、請求項15に記載の医薬組成物。 The pharmaceutical composition according to claim 15 , wherein the aerosol device is a nebulizer or an electrohydrodynamic aerosol device. 請求項816のいずれか1項に記載の医薬組成物を含む吸入器。 An inhaler comprising the pharmaceutical composition according to any one of claims 8 to 16 . 約2μm~約3μmのサイズの液滴を送達するように構成された、請求項17に記載の吸入器。 17. The inhaler of claim 17 , configured to deliver droplets with a size of about 2 μm to about 3 μm.
JP2021505625A 2018-04-12 2019-04-12 Compositions and Methods for Treating Elastic Fibrosis Pending JP2021521280A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862656654P 2018-04-12 2018-04-12
US62/656,654 2018-04-12
PCT/US2019/027257 WO2019200274A1 (en) 2018-04-12 2019-04-12 Compositions and methods for treating elastic fiber breakdown

Publications (2)

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JP2021521280A JP2021521280A (en) 2021-08-26
JPWO2019200274A5 true JPWO2019200274A5 (en) 2022-04-22

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EP (1) EP3773614A1 (en)
JP (1) JP2021521280A (en)
WO (1) WO2019200274A1 (en)

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WO2023285984A1 (en) * 2021-07-14 2023-01-19 Redox-Co S.R.L. Glutahtione c4 against airway affections

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