JP5746721B2 - 同時の化学療法及び免疫療法 - Google Patents
同時の化学療法及び免疫療法 Download PDFInfo
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- JP5746721B2 JP5746721B2 JP2013025374A JP2013025374A JP5746721B2 JP 5746721 B2 JP5746721 B2 JP 5746721B2 JP 2013025374 A JP2013025374 A JP 2013025374A JP 2013025374 A JP2013025374 A JP 2013025374A JP 5746721 B2 JP5746721 B2 JP 5746721B2
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Description
本発明は、癌の免疫治療の領域に関するものである。特に、腫瘍ワクチンに対する応答を増幅することに関する。
積極的な外科的切除、高線量の集中的な放射線治療、及び化学療法にも拘らず、GBMと診断された患者は、診断後15ヶ月より短い生存期間中央値(median survival)を有する(Stupp et al.,Optimal role of temozolomide in the treatment of malignant gliomas. Curr Neurol Neurosci Rep. 2005 May; 5(3):198-206(非特許文献1))。治療の失敗を、少なくとも部分的には、比較的減じられた治療指数に帰することができ、そのため用量を漸増する試みは用量を制限する全身性または神経性の毒性に終わる。免疫治療の使用は、これらの腫瘍の潜在的な治療となる見込みが持たれてきたが、最近まで、臨床的効力を示すものは殆ど無かった。グリオーマ患者の樹状細胞(DC)及び酸溶出ペプチド(Ashkenazi et al., A selective impairment of the IL-2 system in lymphocytes of patients with glioblastomas: increased level of soluble IL-2R and reduced protein tyrosine phosphorylation. Neuroimmunomodulation. 1997(非特許文献2);Kolenko et al.,Tumor-induced suppression of T lymphocyte proliferation coincides with inhibition of Jak3 expression and IL-2 receptor signaling: role of soluble products from human renal cell carcinomas. J Immunol. 1997 Sep 15;159(6):3057-67(非特許文献3);Liau et al.,Dendritic cell vaccination in glioblastoma patients induces systemic and intracranial T-cell responses modulated by the local central nervous system tumor microenvironment. Clin Cancer Res. 2005 Aug 1;11(15):5515-25(非特許文献4))または、抗原特異的ペプチド(Heimberger AB, Archer GE,et al.,Dendritic cells pulsed with a tumor-specific peptide induce long-lasting immunity and are effective against murine intracerebral melanoma. Neurosurgery.2002 Jan;50(1):158-64;discussion 164-6(非特許文献5))によるワクチン接種を含む、選ばれた患者についての幾つかの臨床試験は、生存期間中央値を20〜31ヶ月の範囲に増加させ、有望性を証明した。さらに、抗原特異的免疫治療的アプローチを利用した最近完了した第II相臨床試験では、GBM患者の増殖抑制期間(time to progression; TTP)が15ヶ月に遅延され、これは、7ヶ月のTTP(Stupp et al., 2005,上述(非特許文献1))及び29ヶ月の生存期間中央値(Heimberger et al, J Transl Med. 2005 Oct 19;3:38 The natural history of EGFR and EGFRvIII in glioblastoma patients.(非特許文献6))を有する、放射線治療及びテモゾロミドからなる患者管理の基準と顕著な対照をなす。漸増的に、これらの免疫治療試験により、悪性グリオーマ患者の生来の免疫抑制にも拘らず、効力のある免疫応答を生じさせうることを示唆する。しかしながら、近来確立された患者管理の基準及び全体的に不十分な予後のため、何等かの形の化学治療でGBM患者を処置するのにためらいがある。
対象における腫瘍を処置するための方法が提供される。治療上有効な量のEGFRvIIIペプチド、及び、リンパ球減少を誘導する治療上有効な量の化学療法剤が対象に投与される。
化学療法及び免疫療法の同時適用は、化学療法により誘導されたリンパ球減少が免疫療法の治療効力を削減するとの懸念から、禁忌と考えられてきた。テモゾロミドは、悪性グリオーマ患者のための効果的な化学療法薬として示されてきており、免疫療法で処置するために神経膠芽腫(GBM)患者からこの薬剤を取り上げることには議論の余地がある。通説にも拘らず、本発明者らは、免疫療法の効果を打ち消すことなく、化学療法と免疫療法の両方を同時に行えることを証明する。実際、テモゾロミドにより誘導されたリンパ球減少は、ペプチドワクチンと実のところ相乗的な可能性がある。出願人は、作用機構に関し特定の理論に束縛されることを望まないが、観察された相乗作用は、エフェクター細胞傷害性CD8+T細胞の増加を可能にする、Tregs(制御性T細胞)の阻害またはTregsの回復の失敗に付随的でもよい。他の機構もまた関連してもよい。
または「PEP-3」が例として含まれる。EGFRvIIIペプチドは、いずれの哺乳動物種のEGFRvIII由来の(または、それと配列において対応する)ものであってもよいが、好ましくはヒトのものである。EGFRの特定の野生型配列をSEQ ID NO:6〜9に示す。
のものが含まれ、
式中R1は、水素原子;または、6個までの炭素原子を含む、直鎖アルキル若しくは有枝鎖アルキル、アルケニルまたはアルキニル基を表し、これら各基は、未置換であるか、若しくはハロゲン(即ち、臭素、ヨウ素、または好ましくは塩素若しくはフッ素)原子、4個までの炭素原子を含む直鎖若しくは有枝鎖のアルコキシ(例えば、メトキシ)、アルキルチオ、アルキルスリヒニル(alkylsullihinyl)及びアルキルスルホニル基、並びに、置換されてもよいフェニル基から選択される、1〜3個の置換基により置換されている。または、R1は、シクロアルキル基を表す。そして、R2は、窒素原子、各々4個までの炭素原子を含む直鎖及び有枝鎖のアルキルまたはアルケニル基から選択される1つ若しくは2つの基、並びにシクロアルキル基を伴うカルバモイル基を表し、例えば、メチルカルバモイルまたはジメチルカルバモイル基を表す。記号R1が、2若しくは3個のハロゲン原子により置換されたアルキル、アルケニルまたはアルキニル基を表す場合、前述のハロゲン原子は同じであっても、異なっていてもよい。記号R1が、1、2若しくは3個の任意に置換されたフェニル基により置換されたアルキル、アルケニルまたはアルキニル基を表す場合、1つまたは複数のフェニルラジカル上の任意の置換基は、例えば、4個までの炭素を含む、アルコキシ及びアルキル基(例えば、1つまたは複数のメトキシ及び/またはメチル基)、並びにニトロ基から選択してもよい。記号R1は、例えば、ベンジルまたはp-メトキシベンジル基を表してもよい。R1及びR2の記号の定義内のシクロアルキル基には、3〜8個、好ましくは6個の炭素原子が含まれる。化合物を、塩またはプロドラック、特にR1がHの場合、アルカリ金属塩として提供してもよい。例えば、米国特許第5,260,291号を参照されたい。
。当業者には、本発明を行うのに使用できる多数のバリエーションの外部ビーム治療が、容易に理解できる。例えば、米国特許第6,882,702号、同第6,879,659号、同第6,865,253号、同第6,863,704号、同第6,826,254号、同第6,792,074号、同第6,714,620号及び同第5,528,650号を参照されたい。
化学療法と免疫療法が同時に適用できるという仮説を試験するために、本発明者らは、新たにGBMと診断された患者を、上皮増殖因子変異体III(EGFRvIII)を標的とするペプチドワクチン(Heimberger et al.,2006)を投与すると同時に、標準的な医療であるテモゾロミドを用いて処置した。膜貫通チロシンキナーゼ受容体(Ekstrand et al.,1991)である上皮増殖因子受容体(EGFR)の過剰発現に結びつくEGFR遺伝子の増幅は、変異体EGFR遺伝子であるEGFRvIII(Wikstrand et al.,1997)と関連する。先の仕事により、EGFR増幅が、全てのEGFRvIII発現GBMs(Heimberger et al.,2005)で明らかであり、そして、増幅されたEGFRを欠くGBMsは、EGFRvIIIタンパク質について陽性ではない(Aldape et al.,2004)。
共通惹起抗原(common recall antigen)に対する遅延型過敏症(DTH)の試験、及び、ワクチンの成分を、全ワクチンの開始前、3回目のワクチン後、及び管理サイクルの間、月ごと、26日目に評価した。ワクチンの開始前、並びに、照射及び同時テモゾロミドの完了後、患者はカンジダ属に対してのみ反応性で、ワクチンの成分、PEPvIIIまたはKLHに対してはDTH反応を有さなかった。しかしながら、3回目のワクチン接種後、患者はワクチンのKLH成分に対して反応性になった。10回目のワクチン接種後、そして、同時テモゾロミドを受けている間、患者はワクチンのPEPvIII成分に対して反応性になった。比較として、サイクル化したテモゾロミドなしでワクチンを受けた患者の内(n=22)、15%より少ない患者が、PEPvIII成分に対して結局反応性になった。最新のフォローアップ及び14回目のワクチン接種投与後、患者は、PEPvIII DTH部位が顕著に硬変していた(16×15mm)。これは、この特定の患者において、テモゾロミドがDTH応答の進展にネガティブに影響しなかったことを示唆すると考えられている。
PEPvIII特異的体液性応答が誘導されたかどうかを決定するため、患者から月ごとに血清を得、PEPvIII-Dynabead(登録商標)アッセイで分析する前に-20℃で保存した。PEPvIIIまたはEGFRvIIIの細胞外ドメイン(EGFRvIII-ECD)を、製造者の指示に従って磁性微粒子に共有結合し(Invitrogen, Carlsbad, CA)、患者血清からの特異的抗体を捕獲するのに使用した。全ての血清試料を、最初にリン酸緩衝食塩水(PBS)+0.5%ウシ血清アルブミン(BSA)で1:10に希釈し、そして3連で分析した。特異性を決定するため、PEPvIII結合Dynabeadsで捕獲されるであろう、あらゆる抗PEPvIIIをブロックするために500ngのPEPvIIIペプチドと、追加の試料を15分間プレインキュベートした。ヒト-マウスキメラ抗PEPvIII抗体(81-0.11ng/ml)をスタンダードとして、各アッセイで、陽性(患者試料ACT4)及び陰性(正常ドナー血清)コントロールと共に流した。フローサイトメーターは、PE-FACSマイクロビーズ及び未反応PEPvIII Dynabeadsで標準に合わせた。ワクチン投与の前に、EGFRvIIIに対する検出可能な体液性応答は無かった。ワクチン接種後、平均蛍光強度(MFI)13となる、EGFRvIIIに対するIgG応答の有意の増加があり、そして、テモゾロミド投与にも拘らず、この体液性応答は維持されていた。
PEPvIIIに対してCD8+細胞障害性応答が誘導されたかどうかを決定するために、各白血球搬出からの患者の末梢血単核細胞(PBMC)及び月々のPBMCを、破傷風毒素(QYIKANSKFIGITE)(SEQ ID NO:5)(10μg/ml)(陽性コントロール)、PEP-1(HDTVYCVKGNKELE)(SEQ ID NO:4)(10μg/mL)(陰性コントロール)、PEPvIII(10μg/mL)(ワクチン成分)、またはKLH(10μg/ml)(ワクチン成分)のいずれかで刺激した。1つの陰性コントロールは未刺激細胞を含んでいた。各条件について、γ-インターフェロン(IFN)分泌を含む、対応するアイソタイプコントロールを使用した。全てのウェルを37℃で6時間、細胞内輸送工程を阻止するタンパク質輸送阻害剤であるGolgiplug(商標)(Pharmingen, SanDiego, CA)とインキュベートした。インキュベーション後、細胞を洗浄し、そして精製された抗CD16抗体(Pharmingen)及びウサギ血清(Pharmingen)を用いて、非特異的結合を阻止した。細胞を表面マーカー(CD3、CD4、CD8)について、適当なフルオレセインイソチオシアネート、及びアロフィコシアニン標識蛍光標識一次抗体またはアイソタイプコントロール(Pharmingen)とインキュベートすることにより染色した。その後、細胞はCytofix/Cytoperm(BD Biosciences, San Jose, CA)で固定し、そして、γ-IFNに対するフィコエリスリン標識抗体またはアイソタイプコントロールとインキュベートした。染色後、細胞を洗浄し、Cellquestソフトウェア(BD Immunocytometry systems, San Jose, CA)を用いて、FACSCaliburフローサイトメーター上のフローサイトメトリーにより、最低1×105個の生きた、出入の制御された(gated)事象を評価した。ワクチンを受ける前、患者は未刺激コントロール及びPEP-1陰性コントロールに対し最小の応答であった。ワクチンを受けた後、及びテモゾロミド投与の間、PEPvIII特異的γ-IFN産生CD8+T細胞が増加した。
テモゾロミド(5/21スケジュール)及び同時投与ワクチン(この例では19日目)のサイクルの間の種々のT細胞集団の反応を特徴付けるため、本発明者らは、0、3、5、12、19、23、25及び26日目に末梢血を得た。フロー分析サイトメトリー(flow analysis cytometry)により、免疫化学療法サイクルの間の、CD8+T細胞及びCD4+CD25+FoxP3+制御T細胞サブセットの割合を調べた。FoxP3のFITC標識モノクローナル抗体(mAb)がeBioscienceにより作成されたのを除いて、全ての蛍光結合mAb(PerCP-Cy5.5-CD3、FITC-CD8、APC-CD4及びPE-CD25)を、BD Biosciencesから購入した。末梢血細胞の表面及び細胞内染色を、製造者により提供された標準的な手順に従って行った。結果をFACSCaliburフローサイトメーターで、CellquestProソフトウェア(BD Biosciences)を用いて分析した。CD8+T細胞のサブセットの減退とは対照的に、Treg集団は、3日間のテモゾロミド投与後に増加し始め、12日目に頂点(全CD4+T細胞の内の0.9%)に達した。CD8+T細胞数が回復し始めたのに対し、Tregsは、その後、降下し始め、23日目まで降下し続けた。過程の最後においては、CD8+T細胞及びTreg集団の両方が前処置レベルまで回復した。ワクチン接種は、相対的に減少したTregsの期間中のCD8+細胞障害性T細胞のブーストに結びついた。
過去15ヶ月に亘って、患者は、2ヶ月の間隔をおいて、完全な身体検査及び脳MR画像法を受けた。彼の検査は安定なままで、MR画像法は、再発の事実を示さなかった。彼は障害なく常勤で働いており、そして、100%のカルノフスキー活動尺度(KPS)及び30/30のミニメンタルステータス試験値を示す。彼の神経学的試験は完全に正常である。
Claims (22)
- 対象における腫瘍を処置するための医薬組成物であって、治療上有効な量のEGFRvIIIペプチド、及び治療上有効な量のテモゾロミドまたはその薬学的に許容される塩を含み、EGFRvIIIペプチドがEGFRvIIIタンパク質の10〜30アミノ酸を含み、EGFRvIIIタンパク質の変異したスプライス連結部をつなぐ、医薬組成物。
- EGFRvIIIペプチドがキーホールリンペットヘモシアニン(KLH)に結合されている、請求項1記載の医薬組成物。
- 前記EGFRvIIIペプチドと同時に投与するための有効な量のGM-CSFをアジュバントとしてさらに含む、請求項1記載の医薬組成物。
- EGFRvIIIペプチドが、配列
H-LEEKKGNYVVTDHS-OH (SEQ ID NO: 1)を有する、請求項1記載の医薬組成物。 - EGFRvIIIペプチドが、配列
LEU-GLU-GLU-LYS-LYS-GLY-ASN-TYR-VAL-VAL-THR-ASP-HIS (SEQ ID NO: 2)
を有する、請求項1記載の医薬組成物。 - 腫瘍が悪性グリオーマである、請求項1記載の医薬組成物。
- 腫瘍が星状細胞腫である、請求項1記載の医薬組成物。
- 腫瘍が肺腫瘍である、請求項1記載の医薬組成物。
- 腫瘍が胸部腫瘍である、請求項1記載の医薬組成物。
- 腫瘍が頭部癌及び頚部癌である、請求項1記載の医薬組成物。
- 対象における腫瘍を処置するための医薬組成物であって、治療上有効な量のKLHに結合されたEGFRvIIIペプチド、前記EGFRvIIIペプチドと同時に投与するためのアジュバントとしての有効な量のGM-CSF、及び治療上有効な量のテモゾロミドまたはその薬学的に許容される塩を含み、EGFRvIIIペプチドがEGFRvIIIタンパク質の10〜30アミノ酸を含み、EGFRvIIIタンパク質の変異したスプライス連結部をつなぐ、医薬組成物。
- 腫瘍が悪性グリオーマである、請求項11記載の医薬組成物。
- 腫瘍が星状細胞腫である、請求項11記載の医薬組成物。
- 腫瘍が肺腫瘍である、請求項11記載の医薬組成物。
- 腫瘍が胸部腫瘍である、請求項11記載の医薬組成物。
- 腫瘍が頭部癌及び頚部癌である、請求項11記載の医薬組成物。
- 治療上有効な量のEGFRvIIIペプチドを含む組成物、及び治療上有効な量のテモゾロミドまたはその薬学的に許容される塩を含む組成物を含む、対象における腫瘍を処置するためのキットであって、EGFRvIIIペプチドがEGFRvIIIタンパク質の10〜30アミノ酸を含み、EGFRvIIIタンパク質の変異したスプライス連結部をつなぐ、キット。
- 治療上有効な量のEGFRvIIIペプチドを含む組成物が、前記EGFRvIIIペプチドと同時に投与するための有効な量のGM-CSFをアジュバントとしてさらに含む、請求項17記載のキット。
- 治療上有効な量のKLHに結合されたEGFRvIIIペプチドおよび前記EGFRvIIIペプチドと同時に投与するためのアジュバントとしての有効な量のGM-CSFを含む組成物、及び治療上有効な量のテモゾロミドまたはその薬学的に許容される塩を含む組成物を含む、対象における腫瘍を処置するためのキットであって、EGFRvIIIペプチドがEGFRvIIIタンパク質の10〜30アミノ酸を含み、EGFRvIIIタンパク質の変異したスプライス連結部をつなぐ、キット。
- 治療上有効な量のEGFRvIIIペプチドを含む、対象における腫瘍を処置するための医薬組成物であって、テモゾロミドまたはその薬学的に許容される塩の治療上有効な量とともに対象に投与されることを特徴とし、EGFRvIIIペプチドがEGFRvIIIタンパク質の10〜30アミノ酸を含み、EGFRvIIIタンパク質の変異したスプライス連結部をつなぐ、医薬組成物。
- さらにアジュバントとしての、有効な量のGM-CSFとともに対象に投与されることを特徴とする、請求項20記載の医薬組成物。
- KLHに結合されたEGFRvIIIペプチドの治療上有効な量を含む、対象における腫瘍を処置するための医薬組成物であって、アジュバントとしての有効な量のGM-CSF、及び治療上有効な量のテモゾロミドまたはその薬学的に許容される塩とともに対象に投与されることを特徴とし、EGFRvIIIペプチドがEGFRvIIIタンパク質の10〜30アミノ酸を含み、EGFRvIIIタンパク質の変異したスプライス連結部をつなぐ、医薬組成物。
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US8900816B2 (en) * | 2007-07-19 | 2014-12-02 | Duke University | Assay for anti-EGFRvIII antibodies |
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US9529689B2 (en) | 2009-11-30 | 2016-12-27 | Red Hat, Inc. | Monitoring cloud computing environments |
SE535982C2 (sv) * | 2009-12-15 | 2013-03-19 | Theravac Pharmaceuticals Ab | Ett nytt vaccin som angriper tumörkärl som ett effektivt redskap i tumörterapi |
SG10201408505SA (en) * | 2009-12-22 | 2015-02-27 | Celldex Therapeutics Inc | Vaccine compositions |
CN102309757B (zh) * | 2010-07-09 | 2014-09-17 | 中国科学院上海巴斯德研究所 | Foxp3及调节性t细胞的调节因子及其应用 |
CN103415620B (zh) * | 2010-11-17 | 2016-10-12 | 艾杜罗生物科技公司 | 诱导针对EGFRvIII的免疫应答的方法和组合物 |
TWI386203B (zh) | 2011-01-07 | 2013-02-21 | Univ China Medical | 治療腦癌或用以降低腦癌細胞對替莫唑胺之抗藥性之醫藥組合物及其應用 |
US9757424B2 (en) | 2011-09-27 | 2017-09-12 | Biomed Valley Discoveries, Inc. | Compositions and methods of treating gliomas |
WO2013112881A1 (en) | 2012-01-27 | 2013-08-01 | Thomas Jefferson University | Mct protein inhibitor-related prognostic and therapeutic methods |
CA2919907A1 (en) | 2012-08-02 | 2014-02-06 | The Board Of Trustees Of The Leland Stanford Junior University | Peptide vaccines based on the egfrviii sequence for the treatment of tumors |
US10022372B2 (en) | 2013-04-19 | 2018-07-17 | Thomas Jefferson University | Caveolin-1 related methods for treating glioblastoma with temozolomide |
RU2725135C1 (ru) * | 2019-11-19 | 2020-06-30 | Федеральное государственное бюджетное научное учреждение "Томский национальный исследовательский медицинский центр Российской академии наук" (Томский НИМЦ) | Гемопротекторное средство |
EP4069253A4 (en) * | 2019-12-02 | 2024-01-10 | Phoenix Biotechnology, Inc. | METHOD AND COMPOSITIONS FOR TREATING GLIOBLASTOMA |
JP2023550148A (ja) | 2020-11-20 | 2023-11-30 | シンシア・イノベーション・インコーポレイテッド | がん免疫治療に用いられる武装二重car-t組成物及び方法 |
WO2023235132A1 (en) * | 2022-06-03 | 2023-12-07 | Bluerock Therapeutics Lp | Cell delivery vehicle and methods of using the same |
CN115887450B (zh) * | 2022-12-09 | 2024-06-25 | 杭州师范大学 | 角鲨烯化替莫唑胺的合成及其自组装纳米粒的制备和应用 |
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CA2261433A1 (en) | 1993-12-09 | 1995-06-10 | Belinda Sanchez Ramirez | Composition comprising autologous epidermal growth factor |
WO1996016988A1 (en) * | 1994-11-28 | 1996-06-06 | Thomas Jefferson University | Reagents and processes for targeting mutant epidermal growth factor receptors |
US6503503B1 (en) | 1997-05-13 | 2003-01-07 | Duke University | Allogeneic cellular vaccine |
US5891432A (en) * | 1997-07-29 | 1999-04-06 | The Immune Response Corporation | Membrane-bound cytokine compositions comprising GM=CSF and methods of modulating an immune response using same |
US6645503B1 (en) * | 1998-03-10 | 2003-11-11 | Wyeth Holdings Corporation | Antigenic conjugates of conserved lipopolysaccharides of gram negative bacteria |
DE19842415A1 (de) * | 1998-09-16 | 2000-03-23 | Merck Patent Gmbh | Pharmazeutische Zubereitung |
US6251886B1 (en) * | 1998-12-07 | 2001-06-26 | Schering Corporation | Methods of using temozolomide in the treatment of cancers |
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US20040147428A1 (en) * | 2002-11-15 | 2004-07-29 | Pluenneke John D. | Methods of treatment using an inhibitor of epidermal growth factor receptor |
WO2005043155A1 (en) | 2003-10-21 | 2005-05-12 | Cedars-Sinai Medical Center | System and method for the treatment of cancer, including cancers of the central nervous system |
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WO2005086922A2 (en) * | 2004-03-10 | 2005-09-22 | Board Of Regents, University Of Texas System | Oncolytic adenovirus armed with therapeutic genes |
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US20150118181A1 (en) | 2015-04-30 |
ZA200803759B (en) | 2009-10-28 |
EP1940461A4 (en) | 2009-12-09 |
EP1940461B1 (en) | 2014-01-08 |
RU2008120665A (ru) | 2009-11-27 |
WO2007056061A2 (en) | 2007-05-18 |
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CA2628282C (en) | 2015-04-07 |
CA2628282A1 (en) | 2007-05-18 |
WO2007056061A3 (en) | 2009-05-07 |
KR20080091427A (ko) | 2008-10-13 |
EP1940461A2 (en) | 2008-07-09 |
ES2454990T3 (es) | 2014-04-14 |
DK1940461T3 (da) | 2014-03-31 |
MX2008005640A (es) | 2008-12-09 |
JP2009518287A (ja) | 2009-05-07 |
CN101594877A (zh) | 2009-12-02 |
CN103463630A (zh) | 2013-12-25 |
CN104857500A (zh) | 2015-08-26 |
US9399662B2 (en) | 2016-07-26 |
AU2006312013A8 (en) | 2008-06-19 |
JP2013126994A (ja) | 2013-06-27 |
BRPI0618050A2 (pt) | 2011-08-16 |
US20090220551A1 (en) | 2009-09-03 |
AU2006312013A1 (en) | 2007-05-18 |
NZ567837A (en) | 2011-11-25 |
JP5674273B2 (ja) | 2015-02-25 |
AU2006312013B2 (en) | 2012-10-04 |
US20180215789A1 (en) | 2018-08-02 |
RU2473560C2 (ru) | 2013-01-27 |
IL191158A (en) | 2015-08-31 |
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