JP2010504079A5 - - Google Patents
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- JP2010504079A5 JP2010504079A5 JP2009516634A JP2009516634A JP2010504079A5 JP 2010504079 A5 JP2010504079 A5 JP 2010504079A5 JP 2009516634 A JP2009516634 A JP 2009516634A JP 2009516634 A JP2009516634 A JP 2009516634A JP 2010504079 A5 JP2010504079 A5 JP 2010504079A5
- Authority
- JP
- Japan
- Prior art keywords
- breast cancer
- administration
- subject
- neu
- her2
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 206010006187 Breast cancer Diseases 0.000 claims description 17
- 208000026310 Breast neoplasm Diseases 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 8
- 108090000623 proteins and genes Proteins 0.000 claims description 6
- 230000002950 deficient Effects 0.000 claims description 3
- 230000001105 regulatory effect Effects 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 4
- MDOJTZQKHMAPBK-UHFFFAOYSA-N 4-iodo-3-nitrobenzamide Chemical compound NC(=O)C1=CC=C(I)C([N+]([O-])=O)=C1 MDOJTZQKHMAPBK-UHFFFAOYSA-N 0.000 claims 2
- 101500025419 Homo sapiens Epidermal growth factor Proteins 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 239000002246 antineoplastic agent Substances 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 238000002512 chemotherapy Methods 0.000 claims 2
- 229940127089 cytotoxic agent Drugs 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 102000015694 estrogen receptors Human genes 0.000 claims 2
- 108010038795 estrogen receptors Proteins 0.000 claims 2
- 229940116978 human epidermal growth factor Drugs 0.000 claims 2
- 238000007918 intramuscular administration Methods 0.000 claims 2
- 238000001990 intravenous administration Methods 0.000 claims 2
- GVUGOAYIVIDWIO-UFWWTJHBSA-N nepidermin Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CS)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O)C(C)C)[C@@H](C)CC)C(C)C)C(C)C)C1=CC=C(O)C=C1 GVUGOAYIVIDWIO-UFWWTJHBSA-N 0.000 claims 2
- 238000007911 parenteral administration Methods 0.000 claims 2
- 102000003998 progesterone receptors Human genes 0.000 claims 2
- 108090000468 progesterone receptors Proteins 0.000 claims 2
- 238000001959 radiotherapy Methods 0.000 claims 2
- 238000007920 subcutaneous administration Methods 0.000 claims 2
- 238000001356 surgical procedure Methods 0.000 claims 2
- 238000011282 treatment Methods 0.000 claims 2
- NZBUMQONDVMPDO-UHFFFAOYSA-N 2-iodo-3-nitrobenzamide Chemical compound NC(=O)C1=CC=CC([N+]([O-])=O)=C1I NZBUMQONDVMPDO-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 101710179684 Poly [ADP-ribose] polymerase Proteins 0.000 description 7
- 102100023712 Poly [ADP-ribose] polymerase 1 Human genes 0.000 description 7
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 5
- 239000012661 PARP inhibitor Substances 0.000 description 3
- 229940121906 Poly ADP ribose polymerase inhibitor Drugs 0.000 description 3
- 239000005557 antagonist Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 108700020463 BRCA1 Proteins 0.000 description 1
- 102000036365 BRCA1 Human genes 0.000 description 1
- 101150072950 BRCA1 gene Proteins 0.000 description 1
- 108700020462 BRCA2 Proteins 0.000 description 1
- 102000052609 BRCA2 Human genes 0.000 description 1
- 101150008921 Brca2 gene Proteins 0.000 description 1
- OTAFHZMPRISVEM-UHFFFAOYSA-N chromone Chemical compound C1=CC=C2C(=O)C=COC2=C1 OTAFHZMPRISVEM-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80456306P | 2006-06-12 | 2006-06-12 | |
| US86660206P | 2006-11-20 | 2006-11-20 | |
| PCT/US2007/071053 WO2008147418A1 (en) | 2006-06-12 | 2007-06-12 | Method of treating diseases with parp inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010504079A JP2010504079A (ja) | 2010-02-12 |
| JP2010504079A5 true JP2010504079A5 (enExample) | 2012-04-19 |
Family
ID=40075416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009516634A Pending JP2010504079A (ja) | 2006-06-12 | 2007-06-12 | Parp阻害剤を用いる疾病の治療方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20070292883A1 (enExample) |
| EP (1) | EP2038654A4 (enExample) |
| JP (1) | JP2010504079A (enExample) |
| AU (1) | AU2007354301A1 (enExample) |
| CA (1) | CA2655257A1 (enExample) |
| IL (1) | IL195768A0 (enExample) |
| WO (1) | WO2008147418A1 (enExample) |
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| AU2007292306A1 (en) | 2006-09-05 | 2008-03-13 | Bipar Sciences, Inc. | Inhibition of fatty acid synthesis by PARP inhibitors and methods of treatment thereof |
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| JP6758195B2 (ja) | 2014-01-14 | 2020-09-23 | ネクター セラピューティクス | 併用ベースの治療方法 |
| AU2018275800A1 (en) | 2017-06-02 | 2019-12-19 | The Johns Hopkins University | Detection of PAR in the CSF of patients with Parkinson's disease |
| EP3631448A4 (en) * | 2017-06-02 | 2021-03-03 | The Johns Hopkins University | DETECTION OF PAR IN THE CSF OF PATIENTS WITH PARKINSON'S DISEASE |
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| HRP20120960T1 (hr) * | 2007-01-16 | 2012-12-31 | Bipar Sciences, Inc. | Formulacije za lijeäśenje raka |
| EP2211854A4 (en) * | 2007-10-19 | 2011-01-12 | Bipar Sciences Inc | METHODS AND COMPOSITIONS FOR THE TREATMENT OF CANCER USING BENZOPYRONE-TYPE PARP INHIBITORS |
| KR20100102609A (ko) * | 2007-11-12 | 2010-09-24 | 바이파 사이언스 인코포레이티드 | Parp 억제제를 단독으로 사용하거나 항종양제와 병용하여 유방암을 치료하는 방법 |
| NZ586123A (en) * | 2007-11-12 | 2012-12-21 | Bipar Sciences Inc | Treatment of ovarian cancer with 4-iodo-3-nitrobenzamide in combination with topoisomerase inhibitors |
| CA2708157A1 (en) * | 2007-12-07 | 2009-06-11 | Bipar Sciences, Inc. | Treatment of cancer with combinations of topoisomerase inhibitors and parp inhibitors |
-
2007
- 2007-06-12 EP EP07875034A patent/EP2038654A4/en not_active Withdrawn
- 2007-06-12 US US11/818,210 patent/US20070292883A1/en not_active Abandoned
- 2007-06-12 CA CA002655257A patent/CA2655257A1/en not_active Abandoned
- 2007-06-12 JP JP2009516634A patent/JP2010504079A/ja active Pending
- 2007-06-12 AU AU2007354301A patent/AU2007354301A1/en not_active Withdrawn
- 2007-06-12 WO PCT/US2007/071053 patent/WO2008147418A1/en not_active Ceased
-
2008
- 2008-12-07 IL IL195768A patent/IL195768A0/en unknown
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