JP2020512328A5 - - Google Patents

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JP2020512328A5
JP2020512328A5 JP2019552023A JP2019552023A JP2020512328A5 JP 2020512328 A5 JP2020512328 A5 JP 2020512328A5 JP 2019552023 A JP2019552023 A JP 2019552023A JP 2019552023 A JP2019552023 A JP 2019552023A JP 2020512328 A5 JP2020512328 A5 JP 2020512328A5
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  1. 遊離塩基、共結晶もしくは塩形態の1−(4−フルオロ−フェニル)−4−((6bR,10aS)−3−メチル−2,3,6b,9,10,10a−ヘキサヒドロ−1H,7H−ピリド[3’,4’:4,5]ピロロ[1,2,3−de]キノキサリン−8−イル)−ブタン−1−オン(式Iの化合物)を含むまたは遊離塩基、共結晶もしくは塩形態の1−(4−フルオロ−フェニル)−4−((6bR,10aS)−2,2−d−3−メチル−2,3,6b,9,10,10a−ヘキサヒドロ−1H,7H−ピリド[3’,4’:4,5]ピロロ[1,2,3−de]キノキサリン−8−イル)−ブタン−1−オン(式IIの化合物)を含むまたは遊離塩基、共結晶もしくは塩形態の1−(4−フルオロ−フェニル)−4−((6bR,10aS)−1,1,2,2−d−3−メチル−2,3,6b,9,10,10a−ヘキサヒドロ−1H,7H−ピリド[3’,4’:4,5]ピロロ[1,2,3−de]キノキサリン−8−イル)−ブタン−1−オン(式IIIの化合物)を含む、経粘膜医薬製剤であって、前記製剤が、速溶性錠剤またはウェーハ剤、舌下錠剤またはウェーハ剤、速溶性フィルム剤、舌下フィルム剤または頬側フィルム剤、経口ゲル剤、または速溶性舌下もしくは頬側ゲル剤である、経粘膜医薬製剤。
  2. 製剤が遊離塩基形態の式Iの化合物または式IIの化合物または式IIIの化合物を含む、請求項1に記載の製剤。
  3. 製剤が塩形態の式Iの化合物または式IIの化合物または式IIIの化合物を含む、請求項1に記載の製剤。
  4. 塩形態がトシル酸塩である、請求項3に記載の製剤。
  5. 製剤が0.01〜10mgの式Iの化合物(遊離塩基当量)または式IIの化合物(遊離塩基当量)または式IIIの化合物(遊離塩基当量)を含む、請求項1に記載の製剤。
  6. 1以上の親水性水可溶性または水膨潤性ポリマーをさらに含む、請求項1に記載の製剤。
  7. ポリマーが天然または修飾セルロースポリマー、エチレンオキシドおよび/またはプロピレンオキシドのポリマー、アクリル酸モノマーを含むポリマー、天然または修飾ゴム、天然または修飾デンプンまたはこれらの任意の混合物からなる群から選択される、請求項6に記載の製剤。
  8. 可塑剤、界面活性剤、乾燥剤、香味剤、甘味剤、結合剤、崩壊剤、湿潤剤(humectants)、湿潤剤、抗酸化剤、緩衝剤および濃化剤からなる群から選択される1以上の添加物をさらに含む、請求項1に記載の製剤。
  9. 製剤が速溶性錠剤またはウェーハ剤、または舌下錠剤またはウェーハ剤である、請求項1に記載の製剤。
  10. 製剤が経口スプレー剤、または舌下スプレー剤または頬側スプレー剤である、請求項1に記載の製剤。
  11. 製剤が速溶性フィルム剤、または舌下フィルム剤または頬側フィルム剤である、請求項1に記載の製剤。
  12. フィルム剤が均一または実質的に均一な厚さを有する、請求項11に記載の製剤。
  13. 式Iの化合物または式IIの化合物または式IIIの化合物が、フィルム剤全体に渡って均一にまたは実質的に均一に分散されている、請求項11に記載の製剤。
  14. 製剤が鼻腔内スプレー剤である、請求項1に記載の製剤。
  15. 製剤が経口ゲル剤、または速溶性舌下または頬側ゲル剤である、請求項1に記載の製剤。
  16. 製剤が膣内製剤、または膣内速溶性錠剤、ウェーハ剤またはゲル剤または膣内スプレー剤または膣内速溶性フィルム剤である、請求項1に記載の製剤。
  17. 式Iの化合物または式IIの化合物または式IIIの化合物が微粒子として製剤に取り込まれている、請求項1に記載の製剤。
  18. 式Iの化合物または式IIの化合物または式IIIの化合物がナノ粒子として製剤に取り込まれている、請求項1に記載の製剤。
  19. 製剤が投与後30秒以内に粘膜または溶解により吸収される、請求項1に記載の製剤。
  20. 遊離塩基、共結晶もしくは塩形態の1−(4−フルオロ−フェニル)−4−((6bR,10aS)−3−メチル−2,3,6b,9,10,10a−ヘキサヒドロ−1H,7H−ピリド[3’,4’:4,5]ピロロ[1,2,3−de]キノキサリン−8−イル)−ブタン−1−オン(式Iの化合物)を含むまたは遊離塩基、共結晶もしくは塩形態の1−(4−フルオロ−フェニル)−4−((6bR,10aS)−2,2−d−3−メチル−2,3,6b,9,10,10a−ヘキサヒドロ−1H,7H−ピリド[3’,4’:4,5]ピロロ[1,2,3−de]キノキサリン−8−イル)−ブタン−1−オン(式IIの化合物)を含むまたは遊離塩基、共結晶もしくは塩形態の1−(4−フルオロ−フェニル)−4−((6bR,10aS)−1,1,2,2−d−3−メチル−2,3,6b,9,10,10a−ヘキサヒドロ−1H,7H−ピリド[3’,4’:4,5]ピロロ[1,2,3−de]キノキサリン−8−イル)−ブタン−1−オン(式IIIの化合物)を含む、皮下医薬製剤。
  21. 製剤がトシル酸塩形態の式Iの化合物を含む、請求項1に記載の製剤。
  22. 製剤がトシル酸塩形態の式Iの化合物を含む、請求項9に記載の製剤。
  23. 製剤がトシル酸塩形態の式Iの化合物を含む、請求項11に記載の製剤。
  24. 製剤がトシル酸塩形態の式Iの化合物を含む、請求項20に記載の製剤。
JP2019552023A 2017-03-24 2018-03-23 新規組成物および方法 Active JP7132939B2 (ja)

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US201762476538P 2017-03-24 2017-03-24
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US (5) US10716786B2 (ja)
EP (1) EP3600325A4 (ja)
JP (2) JP7132939B2 (ja)
KR (2) KR20220066988A (ja)
CN (2) CN116327770A (ja)
AU (2) AU2018240540B2 (ja)
BR (1) BR112019019875A2 (ja)
CA (1) CA3054841A1 (ja)
IL (2) IL268970B2 (ja)
MX (3) MX2021013640A (ja)
RU (2) RU2767410C2 (ja)
WO (1) WO2018175969A1 (ja)

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