JP7058345B2 - Bcl-2阻害剤及びMDM2阻害剤の組合せ製品並びに疾患の予防及び/又治療におけるその使用 - Google Patents
Bcl-2阻害剤及びMDM2阻害剤の組合せ製品並びに疾患の予防及び/又治療におけるその使用 Download PDFInfo
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- JP7058345B2 JP7058345B2 JP2020550074A JP2020550074A JP7058345B2 JP 7058345 B2 JP7058345 B2 JP 7058345B2 JP 2020550074 A JP2020550074 A JP 2020550074A JP 2020550074 A JP2020550074 A JP 2020550074A JP 7058345 B2 JP7058345 B2 JP 7058345B2
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- 229940126214 compound 3 Drugs 0.000 description 1
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- 238000001514 detection method Methods 0.000 description 1
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- ACYGYJFTZSAZKR-UHFFFAOYSA-J dicalcium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Ca+2].[Ca+2].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O ACYGYJFTZSAZKR-UHFFFAOYSA-J 0.000 description 1
- 239000001177 diphosphate Substances 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
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- 230000005750 disease progression Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
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- 230000035622 drinking Effects 0.000 description 1
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- QPMDWIOUHQWKHV-ODZAUARKSA-M potassium;(z)-4-hydroxy-4-oxobut-2-enoate Chemical compound [K+].OC(=O)\C=C/C([O-])=O QPMDWIOUHQWKHV-ODZAUARKSA-M 0.000 description 1
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- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
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- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Description
Aは、
Eは、炭素原子であり、且つ
Eは、-C(H)-であり、且つ
Eは、窒素原子であり、且つ
X1、X2及びX3は、それぞれ独立して、-CR8=及び-N=からなる群から選択され;
R1a及びR1bは、それらが結合される炭素原子と合わせて、3員、4員又は5員の任意選択的に置換された脂肪族環を形成するか;又は
R1a及びR1bは、それらが結合される炭素原子と合わせて、4員又は5員の任意選択的に置換されたヘテロシクロを形成し;
R2は、-NO2、-SO2CH3及び-SO2CF3からなる群から選択され;
R2aは、水素及びXからなる群から選択され;
R3は、水素、-CN、-C≡CH及び-N(R4a)(R4b)からなる群から選択され;
R4aは、任意選択的に置換されたC1~6アルキル、任意選択的に置換されたC3~6シクロアルキル、ヘテロシクロ、ヘテロアルキル、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R4bは、水素及びC1~4アルキルからなる群から選択され;
R5は、任意選択的に置換されたC1~6アルキル、ヘテロシクロ、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R6a、R6c、R6e、R6f及びR6gは、それぞれ独立して、水素、任意選択的に置換されたC1~6アルキル、任意選択的に置換されたC3~6シクロアルキル、任意選択的に置換されたアリール、任意選択的に置換されたヘテロアリール、ヘテロシクロ、ヘテロアルキル、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R6b及びR6dは、それぞれ独立して、水素、C1~4アルキル及びハロゲンからなる群から選択され;
R7は、任意選択的に置換されたC1~6アルキル、ヘテロシクロ、ヘテロアルキル、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;及び
R8は、水素及びハロゲンからなる群から選択される)
の化合物又はその薬学的に許容される塩である。
MDM2阻害剤は、以下の構造:
本明細書で使用する場合、用語「MDM2阻害剤」は、MDM2に対する結合について競合する物質、p53タンパク質に対するMDM2の結合に影響を及ぼす物質、MDM2活性を阻害する物質、又はMDM2を分解する物質、又はMDM2レベルを低下させる遺伝子ツールを指す。
Aは、
Eは、炭素原子であり、且つ
Eは、-C(H)-であり、且つ
Eは、窒素原子であり、且つ
X1、X2及びX3は、それぞれ独立して、-CR8=及び-N=からなる群から選択され;
R1a及びR1bは、それらが結合される炭素原子と合わせて、3員、4員又は5員の任意選択的に置換された脂肪族環を形成するか;又は
R1a及びR1bは、それらが結合される炭素原子と合わせて、4員又は5員の任意選択的に置換されたヘテロシクロを形成し;
R2は、-NO2、-SO2CH3及び-SO2CF3からなる群から選択され;
R2aは、水素及びXからなる群から選択され;
R3は、水素、-CN、-C≡CH及び-N(R4a)(R4b)からなる群から選択され;
R4aは、任意選択的に置換されたC1~6アルキル、任意選択的に置換されたC3~6シクロアルキル、ヘテロシクロ、ヘテロアルキル、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R4bは、水素及びC1~4アルキルからなる群から選択され;
R5は、任意選択的に置換されたC1~6アルキル、ヘテロシクロ、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R6a、R6c、R6e、R6f及びR6gは、それぞれ独立して、水素、任意選択的に置換されたC1~6アルキル、任意選択的に置換されたC3~6シクロアルキル、任意選択的に置換されたアリール、任意選択的に置換されたヘテロアリール、ヘテロシクロ、ヘテロアルキル、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R6b及びR6dは、それぞれ独立して、水素、C1~4アルキル及びハロゲンからなる群から選択され;
R7は、任意選択的に置換されたC1~6アルキル、ヘテロシクロ、ヘテロアルキル、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;及び
R8は、水素及びハロゲンからなる群から選択される)
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
Eは、炭素原子であり、且つ
R1a及びR1bは、それらに結合する炭素原子と合わせて、3員、4員又は5員の任意選択的に置換された脂肪族環を形成するか;又は
R1a及びR1bは、それらに結合する炭素原子と合わせて、4員又は5員の任意選択的に置換されたヘテロシクロを形成し;
R2は、-NO2、-SO2CH3及び-SO2CF3からなる群から選択され;
R3は、水素、-CN、-C≡CH及び-N(R4a)(R4b)からなる群から選択され;
R4aは、任意選択的に置換されたC1~6アルキル、ヘテロシクロ、シクロアルキルアルキル及びヘテロシクロアルキルからなる群から選択され;
R4bは、水素及びC1~4アルキルからなる群から選択される)
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
の化合物又はその薬学的に許容される塩若しくは溶媒和物である。
MDM2阻害剤は、APG-115又はその薬学的に許容される塩若しくは溶媒和物である。
MDM2阻害剤は、APG-115又はその薬学的に許容される塩若しくは溶媒和物である。
MDM2阻害剤は、APG-115又はその薬学的に許容される塩若しくは溶媒和物である。
MDM2阻害剤は、APG-115又はその薬学的に許容される塩若しくは溶媒和物である。
本発明は、以下の実施例及び対照実施例によってさらに例証されることになる。しかしながら、これらの実施例及び対照実施例は、単に本発明をより詳細に説明するために使用されるが、本発明を限定することを意図するものではないことが理解されるべきである。
(1)CellTiter-Glo(登録商標)(CTG)細胞増殖アッセイ
抗増殖効果は、CellTiter-Glo(登録商標)(CTG)アッセイによって試験された。細胞を96ウェルプレート中に播種し、異なる濃度の試験物質で24時間処理した。3種の異なる濃度のMDM2阻害剤(例えば、APG-115)と組み合わせて24時間作用させた9種の異なる濃度の化合物6(10-3~101μMの3×勾配、すなわち0.0016、0.0045、0.014、0.041、0.12、0.36、1.1、3.2、10μMにおいて選択された)を使用することにより、薬物と組み合わせた化合物6の効果を試験した。各試験用量は、3つの複製ウェルで試験された。
ヒト腫瘍免疫不全マウスの皮下異種移植腫瘍モデルを細胞接種によって確立した(Gould SE et al.Translational value of mouse models in oncology drug development.Nature medicine.2015 21,431-439;及びSouers AJ et al.ABT-199,a potent and selective BCL-2 inhibitor,achieves antitumor activity while sparing platelets.Nature medicine.2012 19.202-208を参照されたい):対数増殖期の腫瘍細胞を回収し、計数し、1×PBS中で再懸濁し、細胞懸濁液濃度を2.5~5×107/mLに調整した。1mLのシリンジ(4ゲージニードル)を使用して、腫瘍細胞を5~10×106/0.2mL/マウスで免疫不全マウスの右側部に皮下接種した(実験動物は、Beijing Vital River Laboratory Animal Technology Co.,Ltd.SCXK(Beijing)2016-0006から購入された)。全ての動物実験は、GenePharma Co.,Ltd及びAscentage Pharma Group Co.,Ltdの実験動物の使用及び管理実践に厳格に従った。適切なパラメーターの計算は、中国CFDA「Guidelines for Non-Clinical Research Techniques of Cytotoxic Antitumor Drugs」を基準とした。
(1)2-((1H-ピロロ[2,3-b]ピリジン-5-イル)オキシ)-4-(4-((6-(4-クロロフェニル)スピロ[3.5]ノナ-6-エン-7-イル)メチル)ピペラジン-1-イル)-N-((3-ニトロ-4-(((テトラヒドロ-2H-ピラン-4-イル)メチル)アミノ)フェニル)スルホニル)ベンズアミド(化合物3)の合成
(1)実験方法は、実施例1のセクション(1)において記載されるとおりであった。CTG実験において、以下の悪性腫瘍細胞の化合物6単独並びに化合物6及びAPG-115の組合せの細胞生存率(%)値が決定された:OCI-AML-3(急性骨髄性白血病(AML))、MV-4-11(急性骨髄性白血病(AML))、KMS-26(多発性骨髄腫(MM))、KMS-11(多発性骨髄腫(MM))。
図1において示されるとおり、様々な血液学的悪性細胞(AML及びMM細胞を含む)において、化合物6がMDM2阻害剤APG-115と組み合わせて投与されたとき、腫瘍細胞の増殖に対する阻害効果が亢進された。
したがって、インビトロ実験において、化合物6がMDM2阻害剤APG-115と組み合わせて使用されたとき、血液悪性腫瘍に対するインビトロでの抗増殖活性は、亢進され、これは、併用療法後のIC50値の低下を示している。IC50の比較は、組合せ投与の曲線及び単剤投与の曲線により実施され、組合せ投与の曲線が左への移動を示したことが観察された。したがって、化合物6及びAPG-115の組合せは、相乗効果を有した。
(1)実験方法は、実施例1のセクション(2)において記載されるとおりであった。RS4;11は、野生型p53を保有し、MDM2阻害剤の抗腫瘍効果を評価するための理想的なモデルであった。したがって、マウス異種移植腫瘍モデルは、RS4;11腫瘍細胞株により確立され(Gould SE et al.Translational value of mouse models in oncology drug development.Nature medicine.2015 21,431-439.及びSouers AJ et al.ABT-199,a potent and selective BCL-2 inhibitor,achieves antitumor activity while sparing platelets.Nature medicine.2012 19.202-208を参照されたい)、APG-115と組み合わせた化合物6のインビボ抗腫瘍効果が評価された。
このモデルにおいて、APG-115は、50mg/kg、q2dレジメンの用量での投与の21日後に腫瘍増殖阻害効果を示さなかったが;化合物6は、50mg/kg、qdレジメンの用量でこのモデルにおいて優れた抗腫瘍効果を示し、投与の最後(21日目)に17%のT/C値(図2A、表1)を示した。APG-115(50mg/kg、q2d)と組み合わせた12.5又は50mg/kg(qd)の用量の化合物6は、有意な相乗効果をもたらし、2つの組合せの群は、それぞれ投与の最後(21日目)に5%(P<0.01)及び1%(P<0.01)のT/C値及び100%の腫瘍寛解率を示した。
化合物6(50mg/kg)単独及びAPG-115(50mg/kg)単独の各々は、RS4;11モデルにおいてCR(完全腫瘍退縮)を達成しなかった。しかしながら、12.5又は50mg/kgの十分に耐容性を示した用量では、化合物6及びAPG-115の組合せは、RS4;11モデルにおいて部分的腫瘍退縮(PR)及び完全腫瘍退縮(CR)を達成できた。APG-115と組み合わせた化合物6は、著しい副作用を有しなかったが(図2B)、ヒトRS4;11ALLマウス異種移植腫瘍モデルにおいて単剤の抗腫瘍効果を著しく増大させ、且つ相乗効果を示した(50mg/kgの用量の化合物6をAPG-115と組み合わせたとき、相乗効果度は、26.5であり、1よりはるかに大きかった)。したがって、化合物6及びAPG-115の組合せは、急性リンパ性白血病(ALL)を有する患者に臨床的な利益をもたらし得る。
(1)実験方法は、実施例1のセクション(2)において記載されるとおりであった。インビトロ細胞増殖アッセイにおいて、APG-115と組み合わせた化合物6の相乗的な抗増殖活性がOCI-AML-3腫瘍細胞株において観察された。したがって、マウス異種移植腫瘍モデルを、OCI-AML-3腫瘍細胞株を使用してさらに確立して、化合物6及びAPG-115のインビボ抗腫瘍効果を評価した。
図3A及び表2において示されるとおり、25mg/kg又は100mg/kg qdレジメンの用量の化合物6は、投与の11日後に腫瘍増殖阻害を示さなかった。100mg/kg(1日目~4日目)及び50mg/kg(5日目~11日目)q2dレジメンの用量のAPG-115も投与の11日後に腫瘍増殖阻害を示さなかった。しかしながら、APG-115(100mg/kg、q2d)と組み合わせた25又は100mg/kg(qd)の用量の化合物6は、相乗効果をもたらし、2つの組合せの群のT/C値は、それぞれ投与の最後(11日目)に36%(P<0.05)及び23%(P<0.01)に達した。
化合物6又はAPG-115の組合せは、化合物6単独及びAPG-115単独の投与より著しく優れていた。APG-115と組み合わせた化合物6は、著しい副作用を有さず(図3B)、ヒトOCI-AML-3(AML)マウス異種移植腫瘍モデルにおいて単剤の抗腫瘍効果を著しく増大させることができ、著しい相乗効果を有した(APG-115が25又は100mg/kgの化合物6と組み合わせて投与されたとき、相乗効果度は、それぞれ1.72又は2.20であり、両方とも1より大きかった)。したがって、化合物6及びAPG-115の組合せは、急性骨髄性白血病(AML)を有する患者に臨床的な利益をもたらし得る。
(1)実験方法は、実施例1のセクション(2)において記載されるとおりであった。化合物6は、Ascentage Pharma Groupによって開発された選択的BCL-2阻害剤である。この薬剤は、現在、中国及び米国の両方において癌療法に関して臨床開発中である。化合物6と組み合わせたAPG-115の抗増殖活性の亢進は、インビトロでのAML細胞株における細胞ベースアッセイにおいて観察されている。したがって、化合物6及びAPG-115の相乗的な抗白血病効果は、MV-4-11AML異種移植モデルを使用することによってインビボでさらに評価された。
図4A及び表3において示されるとおり、100mg/kg、p.o.、qd×22日の用量で投与された化合物6は、22日目に55.1%のT/C値を達成した。1~7日目及び16~22日目に1日当たり100mg/kgの用量で経口投与されたAPG-115は、67.1%のT/C値を達成した。さらに、APG-115及び化合物6の組合せ治療は、9.1%のT/C値を達成し、これは、溶媒対照群及びいずれかの単剤治療群と比較して統計的に有意であった。相乗効果率は、4.06であり、これは、2つの薬物の組合せが強力な相乗的抗AML効果を有することを示している。APG-115及び化合物6による組合せ治療は、治療の最後に5例の完全腫瘍退縮(CR、83.3%)及び1例の安定な疾患(SD、16.7%)奏効を有して、100%の奏効率を達成できた。全ての治療中、著しい重量減少は観察されなかった(図4B)。
要約すると、APG-115及び選択的BCL-2阻害剤の化合物6による組合せ治療は、相乗的な抗白血病効果を有し、且つさらなる臨床的検討に値する。
(1)AMLの療法に関するAPG-115及び化合物6の組合せの利点は、難治性の播種性MOLM-13-Luc全身性ヒトAMLモデルにおいてさらに評価された。
図5において示されるとおり、100mg/kg、qd×21日での化合物6単独による治療は、生物発光シグナルの迅速な増大によって示されるとおり、この播種性AMLモデルにおいて限定的な抗白血病活性を有した。APG-115単剤による治療は、生物発光シグナルを著しく減少させた。さらに、化合物6とAPG-115との組合せは、生物発光シグナルをさらに減少させた。
MOLM-13-Luc異種移植モデルは、より高度な悪性度及び疾患進行を有する汎発性の全身性腫瘍であることは、注目に値する。これらのデータは、AML療法に関してAPG-115及び化合物6による組合せ治療のより優れた抗白血病活性をさらに実証した。
Claims (10)
- 医薬組成物の形態である、請求項1に記載の組合せ医薬。
- 前記Bcl-2阻害剤及び前記MDM2阻害剤は、それぞれ別々の製剤中にある、請求項1又は2に記載の組合せ医薬。
- 前記Bcl-2阻害剤及び前記MDM2阻害剤は、同時に又は逐次的に投与される、請求項1又は2に記載の組合せ医薬。
- 薬学的に許容される担体、希釈剤又は賦形剤をさらに含む、請求項1又は2に記載の組合せ医薬。
- 錠剤、カプセル剤、顆粒剤、シロップ剤、散剤、トローチ剤、サシェ剤、カシェ剤、エリキシル剤、懸濁剤、乳剤、液剤、噴霧剤、軟膏剤、クリーム剤及び注射剤の形態である、請求項1又は2に記載の組合せ医薬。
- 請求項1~6のいずれか1項に記載の組合せ医薬を含む、疾患の予防及び/又は治療のための医薬組成物であって、前記疾患は癌である、医薬組成物。
- 前記癌は、非ホジキンリンパ腫(NHL)、びまん性大細胞型B細胞リンパ腫(DLBCL)、濾胞性リンパ腫(FL)、急性骨髄性白血病(AML)、急性リンパ性白血病(ALL)、慢性リンパ性白血病(CLL)、多発性骨髄腫(MM)、及び非小細胞肺癌(NSCLC)からなる群から選択される、請求項7に記載の医薬組成物。
- 前記Bcl-2阻害剤又はその薬学的に許容される塩若しくは溶媒和物は、0.0025~1500mg/日の量である、請求項8に記載の医薬組成物。
- 前記MDM2阻害剤又はその薬学的に許容される塩若しくは溶媒和物は、0.005~500mg/日の量である、請求項8に記載の医薬組成物。
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US11478469B2 (en) | 2018-07-31 | 2022-10-25 | Ascentage Pharma (Suzhou) Co., Ltd. | Combination product of BCL-2 inhibitor and MDM2 inhibitor and use thereof in the prevention and/or treatment of diseases |
CN110772521A (zh) | 2018-07-31 | 2020-02-11 | 苏州亚盛药业有限公司 | Bcl-2抑制剂或Bcl-2/Bcl-xL抑制剂与BTK抑制剂的组合产品及其用途 |
KR20200139139A (ko) * | 2018-07-31 | 2020-12-11 | 어센테지 파마 (쑤저우) 컴퍼니 리미티드 | 리툭시맙 및/또는 벤다무스틴과 병용된 Bcl-2 억제제 또는 CHOP와 병용된 Bcl-2 억제제의 시너지적 항종양 효과 |
JP2022501394A (ja) * | 2019-07-26 | 2022-01-06 | アセンテージ ファーマ(スーチョウ)カンパニー,リミティド | Mdm2阻害剤の医薬組成物、並びに疾患を予防及び/又は治療するためのその使用 |
TWI772992B (zh) * | 2019-12-03 | 2022-08-01 | 大陸商蘇州亞盛藥業有限公司 | 作為bcl-2抑制劑的n-(苯基磺醯基)苯甲醯胺及相關化合物 |
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UA126098C2 (uk) | 2022-08-10 |
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US20220031694A1 (en) | 2022-02-03 |
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