JPWO2020043762A5 - - Google Patents

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JPWO2020043762A5
JPWO2020043762A5 JP2021510859A JP2021510859A JPWO2020043762A5 JP WO2020043762 A5 JPWO2020043762 A5 JP WO2020043762A5 JP 2021510859 A JP2021510859 A JP 2021510859A JP 2021510859 A JP2021510859 A JP 2021510859A JP WO2020043762 A5 JPWO2020043762 A5 JP WO2020043762A5
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pharmaceutical composition
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JP7420791B2 (en
JP2021536454A (en
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Priority claimed from EP18191289.0A external-priority patent/EP3616693A1/en
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Claims (31)

HPV16、HPV18、HPV31、HPV33およびHPV58から選択される少なくとも1つのヒトパピローマウイルス(HPV)による女性患者の内部生殖器官の感染の予防または治療に使用するための、セレン酸含有化合物およびクエン酸、酢酸、リンゴ酸、炭酸、硫酸、硝酸、塩酸、果実酸およびそれらの混合物から選択される薬学的に許容される酸を含有する医薬組成物であって、膣内に適用される医薬組成物。 A selenate-containing compound and citric acid, acetic acid, and citric acid, acetic acid, A pharmaceutical composition for intravaginal application, comprising a pharmaceutically acceptable acid selected from malic acid, carbonic acid, sulfuric acid, nitric acid, hydrochloric acid, fruit acids and mixtures thereof. 患者が少なくとも内部生殖器官の領域においてp16陽性、または、p16陽性およびKi-67陽性であり、患者が該領域においてp16陰性、または、p16陰性およびKi-67陰性になるまで適用される、請求項1に記載の医薬組成物。 The patient is p16 positive , or p16 positive and Ki-67 positive in at least a region of the internal reproductive organs, until the patient is p16 negative , or p16 negative and Ki-67 negative in said region. 1. The pharmaceutical composition according to 1. 全セレン含量が、組成物5ml当たり0.01mg~1.25mgである請求項1または2に記載の医薬組成物。 A pharmaceutical composition according to claim 1 or 2 , wherein the total selenium content is between 0.01 mg and 1.25 mg per 5 ml of composition. 全セレン含量が、組成物5ml当たり0.025mg~1.00mgである請求項1または2に記載の医薬組成物。A pharmaceutical composition according to claim 1 or 2, wherein the total selenium content is between 0.025 mg and 1.00 mg per 5 ml of composition. 全セレン含量が、組成物5ml当たり0.05mg~0.75mgである請求項1または2に記載の医薬組成物。A pharmaceutical composition according to claim 1 or 2, wherein the total selenium content is between 0.05 mg and 0.75 mg per 5 ml of composition. 全セレン含量が、組成物5ml当たり0.10mg~0.50mgである請求項1または2に記載の医薬組成物。A pharmaceutical composition according to claim 1 or 2, wherein the total selenium content is between 0.10 mg and 0.50 mg per 5 ml of composition. 全セレン含量が、組成物5ml当たり0.15mg~0.40mgである請求項1または2に記載の医薬組成物。A pharmaceutical composition according to claim 1 or 2, wherein the total selenium content is between 0.15 mg and 0.40 mg per 5 ml of composition. 全セレン含量が、組成物5ml当たり0.20mg~0.30mgである請求項1または2に記載の医薬組成物。A pharmaceutical composition according to claim 1 or 2, wherein the total selenium content is between 0.20 mg and 0.30 mg per 5 ml of composition. 全セレン用量が、適用当たり0.01mg~1.25mgである請求項1~8のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 8 , wherein the total selenium dose is between 0.01 mg and 1.25 mg per application. 全セレン用量が、適用当たり0.025mg~1.00mgである請求項1~8のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 8, wherein the total selenium dose is between 0.025 mg and 1.00 mg per application. 全セレン用量が、適用当たり0.05mg~0.75mgである請求項1~8のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 8, wherein the total selenium dose is between 0.05 mg and 0.75 mg per application. 全セレン用量が、適用当たり0.10mg~0.50mgである請求項1~8のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 8, wherein the total selenium dose is between 0.10 mg and 0.50 mg per application. 全セレン用量が、適用当たり0.15mg~0.40mgである請求項1~8のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 8, wherein the total selenium dose is between 0.15 mg and 0.40 mg per application. 全セレン用量が、適用当たり0.20mg~0.30mgである請求項1~8のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 8, wherein the total selenium dose is between 0.20 mg and 0.30 mg per application. 組成物が1日に少なくとも1回適用され、任意選択で、該適用は患者の月経中に中止される、請求項1~14のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 14 , wherein the composition is applied at least once a day and optionally said application is discontinued during the patient's menstruation. 組成物が少なくとも30日間適用され、任意選択で、該適用は患者の月経中に中止される、請求項1~14のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 14, wherein the composition is applied for at least 30 days and optionally said application is discontinued during the patient's menstruation. 組成物が少なくとも60日間適用され、任意選択で、該適用は患者の月経中に中止される、請求項1~14のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 14, wherein the composition is applied for at least 60 days and optionally said application is discontinued during the patient's menstruation. 組成物が少なくとも90日間適用され、任意選択で、該適用は患者の月経中に中止される、請求項1~14のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 14, wherein the composition is applied for at least 90 days and optionally said application is discontinued during the patient's menstruation. 前記組成物が1日1回適用され、任意選択で、該適用は、患者の月経中に中止される、請求項1~18のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 18 , wherein said composition is applied once daily, optionally said application is discontinued during the patient's menstruation. 前記適用が患者の月経中に中止される、請求項1~19のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 19 , wherein said application is discontinued during the patient's menstruation. 前記組成物が、前記内部生殖器の感染がもはや検出されなくなるまで適用される、請求項1~20のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 20 , wherein said composition is applied until the internal genital tract infection is no longer detected. 前記組成物が、ゲル、懸濁液、エマルジョン、ゼラチンカプセル若しくはゼラチンを含まないカプセルなどの坐剤、噴霧または粉末の形態で存在する、請求項1~21のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 21 , wherein said composition is in the form of a gel, suspension, emulsion, suppository such as a gelatin or gelatin-free capsule, a spray or a powder. thing. 前記組成物が、二酸化ケイ素をさらに含有する、請求項1~22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 1-22, wherein said composition further comprises silicon dioxide. 前記組成物が、高分散二酸化ケイ素をさらに含有する、請求項1~22のいずれか1項に記載の医薬組成物。A pharmaceutical composition according to any one of claims 1 to 22, wherein said composition further comprises highly dispersed silicon dioxide. 7.0未満のpHを有する、請求項1~24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 1-24, having a pH of less than 7.0. 5.0未満のpHを有する、請求項1~24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 1-24, having a pH of less than 5.0. 4.0~2.5のpHを有する、請求項1~24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 1-24, having a pH of 4.0-2.5. 薬学的に許容される酸がクエン酸である請求項1~27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 1-27, wherein the pharmaceutically acceptable acid is citric acid. 前記亜セレン酸塩含有化合物が、亜セレン酸ナトリウムである請求項1~28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 1-28, wherein the selenite-containing compound is sodium selenite. 内部生殖器官が患者の膣または子宮頸部である請求項1~29のいずれか1項に記載の医薬組成物。 A pharmaceutical composition according to any one of claims 1 to 29 , wherein the internal reproductive organ is the patient's vagina or cervix. 患者がHPV感染以外の癌および/または慢性ウイルス疾患を有さず、および/または患者が免疫抑制されていない、請求項1~30のいずれか1項に記載の医薬組成物。 Pharmaceutical composition according to any one of claims 1 to 30 , wherein the patient does not have cancer and/or chronic viral diseases other than HPV infection and/or the patient is not immunosuppressed.
JP2021510859A 2018-08-28 2019-08-28 Treatment of high-risk human papillomavirus infections Active JP7420791B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP18191289.0 2018-08-28
EP18191289.0A EP3616693A1 (en) 2018-08-28 2018-08-28 Therapy of high-risk human papillomavirus infections
PCT/EP2019/072926 WO2020043762A1 (en) 2018-08-28 2019-08-28 Therapy of high-risk human papillomavirus infections

Publications (3)

Publication Number Publication Date
JP2021536454A JP2021536454A (en) 2021-12-27
JPWO2020043762A5 true JPWO2020043762A5 (en) 2022-08-10
JP7420791B2 JP7420791B2 (en) 2024-01-23

Family

ID=63442535

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Application Number Title Priority Date Filing Date
JP2021510859A Active JP7420791B2 (en) 2018-08-28 2019-08-28 Treatment of high-risk human papillomavirus infections

Country Status (23)

Country Link
US (1) US20210299163A1 (en)
EP (2) EP3616693A1 (en)
JP (1) JP7420791B2 (en)
CN (1) CN112584828A (en)
AR (1) AR116027A1 (en)
AU (1) AU2019332079A1 (en)
BR (1) BR112021003360A2 (en)
CA (1) CA3107691A1 (en)
CL (1) CL2021000197A1 (en)
EA (1) EA202190441A1 (en)
ES (1) ES2958808T3 (en)
GE (1) GEP20227432B (en)
HR (1) HRP20231470T1 (en)
HU (1) HUE064691T2 (en)
IL (1) IL281080A (en)
MA (1) MA53482B1 (en)
MD (1) MD3843715T2 (en)
MX (1) MX2021002310A (en)
PL (1) PL3843715T3 (en)
RS (1) RS64916B1 (en)
TW (1) TWI827652B (en)
UA (1) UA127632C2 (en)
WO (1) WO2020043762A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3875083A1 (en) * 2020-03-03 2021-09-08 Selo Medical GmbH Composition for use in a treatment of cervical cell abnormalities comprising selenite compound and acid

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2001259927B2 (en) 2000-05-10 2005-02-24 Okopharm Forschungs-Und Entwicklungs-Gmbh Method for reducing the surface of silicon dioxide
AT412758B (en) 2000-06-05 2005-07-25 Vis Vitalis Lizenz & Handels USE OF A SELENICITY SOLUTION TO TREAT VIRAL DISEASES
AT412448B (en) * 2001-02-13 2005-03-25 Vis Vitalis Lizenz & Handels USE OF SEXY PREPARATIONS
AT412703B (en) * 2001-12-04 2005-06-27 Vis Vitalis Lizenz & Handels USE OF SELIGENICAL PREPARATIONS FOR TOPICAL OR BUCCAL USE
AT511159A1 (en) * 2011-02-16 2012-09-15 Selo Medical Gmbh PHARMACEUTICAL COMPOSITIONS CONTAIN SELENIC OR SELENATE COMPOUNDS

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