JP2022518174A - 放射線皮膚炎の予防及び治療、並びに皮膚ライトニング、皮膚ホワイトニング、並びに皮膚改善のためのn-アセチルシステインアミド(naca)及び(2r,2r’)-3,3’-ジスルファンジイルビス(2-アセトアミドプロパンアミド)(dinaca) - Google Patents
放射線皮膚炎の予防及び治療、並びに皮膚ライトニング、皮膚ホワイトニング、並びに皮膚改善のためのn-アセチルシステインアミド(naca)及び(2r,2r’)-3,3’-ジスルファンジイルビス(2-アセトアミドプロパンアミド)(dinaca) Download PDFInfo
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Abstract
Description
本出願は、2019年1月11日に出願された米国仮出願第62/791422号明細書の優先権を主張し、その全内容は参照により本明細書に組み込まれる。
無し。
これらの酵素の多くでは、最適な基質は各RがHである過酸化水素であるが、その他は脂質ペルオキシドなどの有機ヒドロペルオキシドでより活性がある。ペルオキシダーゼは、活性部位におけるヘム補因子又は酸化還元活性システイン又はセレノシステイン残基を含有することができる。
Claims (23)
- 放射線皮膚炎の予防及び治療、又は皮膚ライトニング、ホワイトニング、又は皮膚の改善を必要とするヒト患者を特定するステップ、及び
前記ヒト患者に治療有効量のN-アセチルシステインアミド(NACA)又はdiNACAを投与するステップ
を含む、ヒト対象における放射線皮膚炎、皮膚ライトニング、放射線による皮膚への損傷のうちの少なくとも1つの予防及び治療、ホワイトニング、又は皮膚の健康の改善のための、N-アセチルシステイン(NAC)、N-アセチルシステインアミド(NACA)、又は(2R、2R')-3,3'-ジスルファンジイルビス(2-アセトアミドプロパンアミド)(diNACA)の使用のための方法。 - NAC、NACA、又はdiNACAが、薬学的に許容される担体中において、又は薬学的に許容される担体と共に提供される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、経口、静脈内、筋肉内、経腸、眼内、網膜下、硝子体内、局所、眼、舌下、皮膚、皮下、又は直腸内に投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、約0.5~150mg/Kgの1日用量で投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、1日2回又は3回投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、第2の活性薬剤と共に投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、アスコルビン酸、システイン塩酸塩、硫酸水素ナトリウム、二亜硫酸ナトリウム、亜硫酸ナトリウム、パルミチン酸アスコルビル、ブチル化ヒドロキシアニソール(BHA)、ブチル化ヒドロキシトルエン(BHT)、レシチン、没食子酸プロピル、α-トコフェロール、クエン酸、エチレンジアミン四酢酸(EDTA)、ソルビトール、酒石酸、又はリン酸のうちの少なくとも1つから選択される第2の活性薬剤と共に投与される、請求項1に記載の方法。
- 投与のための用量が、1用量当たり100、150、150、300、333、400、500、600、700、750、800、900、1,000、2,500、5,000、7,500、又は10,000mgである、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、ミニ錠剤、カプセル、錠剤、発泡剤、デュアル放出、混合放出、サシェ、粉末、又は液剤によって経口的に送達される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、放射線皮膚炎を予防及び治療するために予防的に投与される、請求項1に記載の方法。
- 治療有効量が、好ましくは、夜間視力の欠損、全体的な視力の欠損、視野の欠損のうちの少なくとも1つを、2週間、1カ月、2カ月、3カ月、6カ月、1年、2年、又は5年のうちの少なくとも1つから選択される規定された期間にわたり、未治療の対照対象と比較して少なくとも10%、少なくとも15%、少なくとも20%、少なくとも25%、少なくとも30%、少なくとも35%、少なくとも40%、少なくとも45%、少なくとも50%、少なくとも55%、少なくとも60%、少なくとも65%、少なくとも70%、少なくとも75%、少なくとも80%、少なくとも85%、少なくとも90%、少なくとも95%、又はそれ以上減少させる治療薬の量を意味する、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、薬学的に許容される担体中において、又は薬学的に許容される担体と共に提供される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、経口、静脈内、筋肉内、鼻腔内、経腸、眼内、網膜下、硝子体内、局所、舌下、又は直腸内に投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが約0.5~150mg/Kgの1日用量で投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが1日2回又は3回投与される、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、アスコルビン酸、システイン塩酸塩、硫酸水素ナトリウム、二亜硫酸ナトリウム、亜硫酸ナトリウム、パルミチン酸アスコルビル、ブチル化ヒドロキシアニソール(BHA)、ブチル化ヒドロキシトルエン(BHT)、レシチン、没食子酸プロピル、α-トコフェロール、クエン酸、エチレンジアミン四酢酸(EDTA)、ソルビトール、酒石酸、又はリン酸のうちの少なくとも1つから選択される第2の活性薬剤と共に投与される、請求項1に記載の方法。
- 投与のための用量が、1用量当たり100、150、150、300、333、400、500、600、700、750、800、900、1,000、2,500、5,000、7,500、又は10,000mgである、請求項1に記載の方法。
- NAC、NACA、又はdiNACAが、ミニ錠剤、カプセル、錠剤、発泡剤、デュアル放出、混合放出、サシェ、粉末、又は液剤によって経口的に送達される、請求項1に記載の方法。
- 治療有効量が、好ましくは、全体的な視力の欠損、視野の欠損を、2週間、1カ月、2カ月、3カ月、6カ月、1年、2年、又は5年のうちの少なくとも1つから選択される規定された期間にわたり、未治療の対照対象と比較して少なくとも10%、少なくとも15%、少なくとも20%、少なくとも25%、少なくとも30%、少なくとも35%、少なくとも40%、少なくとも45%、少なくとも50%、少なくとも55%、少なくとも60%、少なくとも65%、少なくとも70%、少なくとも75%、少なくとも80%、少なくとも85%、少なくとも90%、少なくとも95%、又はそれ以上減少させる治療薬の量を意味する、請求項1に記載の方法。
- 日光曝露からの放射線による皮膚への損傷を防ぐために、NACA又はdiNACAを製剤に添加するステップをさらに含む、請求項1に記載の方法。
- 生物兵器への曝露、化学熱傷、熱傷、摩擦によって引き起こされる接触損傷を防ぐために、NACA又はdiNACAを製剤に添加するステップをさらに含む、請求項1に記載の方法。
- 色素性乾皮症を治療するために、NACA又はdiNACAを製剤に添加するステップをさらに含む、請求項1に記載の方法。
- 酸化的ストレスによって引き起こされるその他の皮膚障害を治療するために、NACA又はdiNACAを製剤に添加するステップをさらに含む、請求項1に記載の方法。
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US201962791422P | 2019-01-11 | 2019-01-11 | |
US62/791,422 | 2019-01-11 | ||
PCT/US2020/012975 WO2020146666A1 (en) | 2019-01-11 | 2020-01-09 | N-acetylcysteine amide (naca) and (2r,2r')-3,3'-disulfanediyl bis (2-acetamidopropanamide) (dinaca) for the prevention and treatment of radiation dermatitis and skin lightening, skin whitening and skin improvement |
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JP2022518174A true JP2022518174A (ja) | 2022-03-14 |
JPWO2020146666A5 JPWO2020146666A5 (ja) | 2023-01-20 |
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EP (1) | EP3908271A4 (ja) |
JP (1) | JP2022518174A (ja) |
KR (1) | KR20210114460A (ja) |
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US20190135741A1 (en) | 2017-11-09 | 2019-05-09 | Nacuity Pharmaceuticals, Inc. | Methods of Making Deuterium-Enriched N-acetylcysteine Amide (D-NACA) and (2R, 2R')-3,3'-Disulfanediyl BIS(2-Acetamidopropanamide) (DINACA) and Using D-NACA and DINACA to Treat Diseases Involving Oxidative Stress |
AU2020206139A1 (en) | 2019-01-11 | 2021-07-29 | Nacuity Pharmaceuticals, Inc. | Treatment of age-related macular degeneration, glaucoma, and diabetic retinopathy with N-acetylicysteine amide (NACA) or 2R,2R')-3-3'-disulfanediyl bis (2-acetamidopropanamide) (diNACA) |
EP4093389A4 (en) * | 2020-01-24 | 2024-02-21 | Nacuity Pharmaceuticals Inc | PRODRUG FOR THE TREATMENT OF DISEASES AND INJURIES OF OXIDATIVE STRESS |
WO2024013711A1 (en) | 2022-07-15 | 2024-01-18 | Universidade De Coimbra | Topical composition and uses thereof |
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AU2006238888A1 (en) * | 2005-04-21 | 2006-11-02 | Glenn A. Goldstein | N-acetylcysteine amide (NAC amide) for the treatment of diseases and conditions associated with oxidative stress |
WO2011044230A2 (en) * | 2009-10-06 | 2011-04-14 | Goldstein Glenn A | N-acetylcysteine amide (nac amide) for the treatment of diseases and conditions |
EP2397125A1 (en) * | 2010-06-15 | 2011-12-21 | Histocell, S.L. | Antioxidant composition |
WO2013138744A1 (en) * | 2012-03-16 | 2013-09-19 | M. Alphabet 1, Llc | Compositions for the treatment of skin disorders |
CN108618993B (zh) * | 2018-07-16 | 2021-07-27 | 广东格烯生物科技股份有限公司 | 一种美白组合物及其制备方法和应用 |
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- 2020-01-09 KR KR1020217025541A patent/KR20210114460A/ko not_active Application Discontinuation
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CN113573704A (zh) | 2021-10-29 |
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EP3908271A4 (en) | 2022-10-26 |
US20220105056A1 (en) | 2022-04-07 |
WO2020146666A1 (en) | 2020-07-16 |
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