JP2018531936A5 - - Google Patents
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- JP2018531936A5 JP2018531936A5 JP2018516772A JP2018516772A JP2018531936A5 JP 2018531936 A5 JP2018531936 A5 JP 2018531936A5 JP 2018516772 A JP2018516772 A JP 2018516772A JP 2018516772 A JP2018516772 A JP 2018516772A JP 2018531936 A5 JP2018531936 A5 JP 2018531936A5
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- reg3α
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- 238000000034 method Methods 0.000 claims description 415
- 108091034117 Oligonucleotide Proteins 0.000 claims description 188
- 101700026522 SMAD7 Proteins 0.000 claims description 181
- 102000049873 Smad7 Human genes 0.000 claims description 181
- 239000000074 antisense oligonucleotide Substances 0.000 claims description 181
- 238000012230 antisense oligonucleotides Methods 0.000 claims description 181
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 128
- 230000007423 decrease Effects 0.000 claims description 116
- 108010002616 Interleukin-5 Proteins 0.000 claims description 84
- 102000003816 Interleukin-13 Human genes 0.000 claims description 83
- 108090000176 Interleukin-13 Proteins 0.000 claims description 83
- 102100024484 Codanin-1 Human genes 0.000 claims description 33
- 101000980888 Homo sapiens Codanin-1 Proteins 0.000 claims description 33
- 208000004998 Abdominal Pain Diseases 0.000 claims description 28
- 239000007788 liquid Substances 0.000 claims description 28
- 239000002773 nucleotide Substances 0.000 claims description 25
- 125000003729 nucleotide group Chemical group 0.000 claims description 25
- 206010012735 Diarrhoea Diseases 0.000 claims description 20
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 18
- 208000011231 Crohn disease Diseases 0.000 claims description 16
- 231100000682 maximum tolerated dose Toxicity 0.000 claims description 14
- LUCHPKXVUGJYGU-XLPZGREQSA-N 5-methyl-2'-deoxycytidine Chemical compound O=C1N=C(N)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 LUCHPKXVUGJYGU-XLPZGREQSA-N 0.000 claims description 10
- 206010009900 Colitis ulcerative Diseases 0.000 claims description 10
- 238000002965 ELISA Methods 0.000 claims description 10
- 101000652166 Homo sapiens Mothers against decapentaplegic homolog 7 Proteins 0.000 claims description 10
- 108090001007 Interleukin-8 Proteins 0.000 claims description 10
- 108060008682 Tumor Necrosis Factor Proteins 0.000 claims description 10
- 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 claims description 10
- 201000006704 Ulcerative Colitis Diseases 0.000 claims description 10
- 238000004458 analytical method Methods 0.000 claims description 10
- 102000044356 human SMAD7 Human genes 0.000 claims description 10
- 239000003246 corticosteroid Substances 0.000 claims description 9
- 210000004369 blood Anatomy 0.000 claims description 5
- 239000008280 blood Substances 0.000 claims description 5
- 238000012544 monitoring process Methods 0.000 claims description 5
- 210000002966 serum Anatomy 0.000 claims description 5
- 229960001334 corticosteroids Drugs 0.000 claims description 3
- 230000003247 decreasing effect Effects 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims 58
- 102100036848 C-C motif chemokine 20 Human genes 0.000 claims 2
- 101000713099 Homo sapiens C-C motif chemokine 20 Proteins 0.000 claims 2
- 101000853002 Homo sapiens Interleukin-25 Proteins 0.000 claims 2
- 101001128431 Homo sapiens Myeloid-derived growth factor Proteins 0.000 claims 2
- 108020000948 Antisense Oligonucleotides Proteins 0.000 claims 1
- 108091058543 REG3 Proteins 0.000 claims 1
- 102100027336 Regenerating islet-derived protein 3-alpha Human genes 0.000 claims 1
- 102000000743 Interleukin-5 Human genes 0.000 description 82
- 229940100602 interleukin-5 Drugs 0.000 description 82
- 102000013691 Interleukin-17 Human genes 0.000 description 81
- 108050003558 Interleukin-17 Proteins 0.000 description 81
- 108010074051 C-Reactive Protein Proteins 0.000 description 9
- 102100032752 C-reactive protein Human genes 0.000 description 9
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 8
- 102000004890 Interleukin-8 Human genes 0.000 description 8
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 4
- 229960004909 aminosalicylic acid Drugs 0.000 description 4
- 239000003018 immunosuppressive agent Substances 0.000 description 4
- 229940124624 oral corticosteroid Drugs 0.000 description 4
- 229960005489 paracetamol Drugs 0.000 description 4
- 210000002381 plasma Anatomy 0.000 description 4
- 229960003444 immunosuppressant agent Drugs 0.000 description 3
- 230000001861 immunosuppressant effect Effects 0.000 description 3
- 102000019034 Chemokines Human genes 0.000 description 1
- 108010012236 Chemokines Proteins 0.000 description 1
- 102000003814 Interleukin-10 Human genes 0.000 description 1
- 108090000174 Interleukin-10 Proteins 0.000 description 1
- 102000001109 Leukocyte L1 Antigen Complex Human genes 0.000 description 1
- 108010069316 Leukocyte L1 Antigen Complex Proteins 0.000 description 1
- 102000008080 Pancreatitis-Associated Proteins Human genes 0.000 description 1
- 108010074467 Pancreatitis-Associated Proteins Proteins 0.000 description 1
- 230000002550 fecal effect Effects 0.000 description 1
- 229940125721 immunosuppressive agent Drugs 0.000 description 1
- 229940096397 interleukin-8 Drugs 0.000 description 1
- XKTZWUACRZHVAN-VADRZIEHSA-N interleukin-8 Chemical compound C([C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@@H](NC(C)=O)CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CCSC)C(=O)N1[C@H](CCC1)C(=O)N1[C@H](CCC1)C(=O)N[C@@H](C)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC=1C=CC(O)=CC=1)C(=O)N[C@H](CO)C(=O)N1[C@H](CCC1)C(N)=O)C1=CC=CC=C1 XKTZWUACRZHVAN-VADRZIEHSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562235556P | 2015-09-30 | 2015-09-30 | |
| US62/235,556 | 2015-09-30 | ||
| PCT/EP2016/073518 WO2017055611A2 (en) | 2015-09-30 | 2016-09-30 | Methods of using smad7 antisense oligonucleotides based on biomarker expression |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018531936A JP2018531936A (ja) | 2018-11-01 |
| JP2018531936A5 true JP2018531936A5 (https=) | 2019-11-07 |
Family
ID=57113318
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018516772A Pending JP2018531936A (ja) | 2015-09-30 | 2016-09-30 | バイオマーカー発現に基づいてｓｍａｄ７アンチセンスオリゴヌクレオチドを使用する方法 |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP3355896A2 (https=) |
| JP (1) | JP2018531936A (https=) |
| CA (1) | CA3000569A1 (https=) |
| WO (1) | WO2017055611A2 (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITRM20030149A1 (it) | 2003-04-02 | 2004-10-03 | Giuliani Spa | Oligonucleotidi (odn) antisenso per smad7 e loro usi in campo medico |
| RU2593939C2 (ru) | 2008-11-13 | 2016-08-10 | Ногра Фарма Лимитед | Антисмысловые композиции и способы их получения и применения |
| JP6389122B2 (ja) | 2011-09-15 | 2018-09-12 | ノグラ ファーマ リミテッド | 抗ｓｍａｄ７治療に対する応答性をモニターするための方法 |
| CN107252492A (zh) | 2012-04-18 | 2017-10-17 | 诺格尔制药有限公司 | 治疗糖尿病和/或促进胰岛移植后存活的方法 |
| US10006029B2 (en) | 2013-03-15 | 2018-06-26 | Nogra Pharma Limited | Methods of treating colorectal cancer |
| AU2015257589A1 (en) | 2014-05-09 | 2016-11-24 | Nogra Pharma Limited | Methods for treating inflammatory bowel disease |
| EP3207136A1 (en) | 2014-10-17 | 2017-08-23 | Nogra Pharma Limited | Methods and compositions for treating a subject with a smad7 antisense oligonucleotide |
| EP3420082A4 (en) | 2016-02-23 | 2019-10-16 | Celgene Alpine Investment Company II, LLC | METHOD FOR THE TREATMENT OF DARM FIBROSIS USING SMAD7 INHIBITION |
| JP2020528910A (ja) * | 2017-07-28 | 2020-10-01 | セルジーン コーポレイション | オリゴヌクレオチド化合物の調製方法 |
| US20220267428A1 (en) * | 2018-10-10 | 2022-08-25 | The Board Of Trustees Of The Leland Stanford Junior University | BLOCKADE OF RGMb FOR TREATING INFLAMMATORY BOWEL DISEASE AND COLITIS |
| CN118649163A (zh) * | 2018-11-30 | 2024-09-17 | 艾尼纳制药公司 | 治疗与s1p1受体有关的病况的方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060135610A1 (en) * | 2004-12-22 | 2006-06-22 | Bortz Jonathan D | Cardiovascular compositions |
| FI20075968A0 (fi) * | 2007-12-28 | 2007-12-28 | Licentia Oy | Menetelmä immunomodulaattorihoitojen tehokkuuden tarkkailemiseksi |
| JP2012507723A (ja) * | 2008-11-03 | 2012-03-29 | シェーリング コーポレイション | 炎症性腸疾患生物マーカーおよび関連治療方法 |
| RU2593939C2 (ru) * | 2008-11-13 | 2016-08-10 | Ногра Фарма Лимитед | Антисмысловые композиции и способы их получения и применения |
| CN103619880A (zh) * | 2011-04-29 | 2014-03-05 | 百时美施贵宝公司 | Ip-10抗体剂量递增方法 |
| JP6389122B2 (ja) * | 2011-09-15 | 2018-09-12 | ノグラ ファーマ リミテッド | 抗ｓｍａｄ７治療に対する応答性をモニターするための方法 |
-
2016
- 2016-09-30 CA CA3000569A patent/CA3000569A1/en not_active Abandoned
- 2016-09-30 EP EP16778306.7A patent/EP3355896A2/en not_active Withdrawn
- 2016-09-30 WO PCT/EP2016/073518 patent/WO2017055611A2/en not_active Ceased
- 2016-09-30 JP JP2018516772A patent/JP2018531936A/ja active Pending
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