ES2385251A1 - Adenovirus oncolíticos para el tratamiento del cáncer. - Google Patents
Adenovirus oncolíticos para el tratamiento del cáncer. Download PDFInfo
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- ES2385251A1 ES2385251A1 ES200901201A ES200901201A ES2385251A1 ES 2385251 A1 ES2385251 A1 ES 2385251A1 ES 200901201 A ES200901201 A ES 200901201A ES 200901201 A ES200901201 A ES 200901201A ES 2385251 A1 ES2385251 A1 ES 2385251A1
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- C12N9/2474—Hyaluronoglucosaminidase (3.2.1.35), i.e. hyaluronidase
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- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10341—Use of virus, viral particle or viral elements as a vector
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- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10371—Demonstrated in vivo effect
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Abstract
Adenovirus oncolíticos para el tratamiento del cáncer.La invención se refiere a un adenovirus oncolítico que comprende una secuencia que codifica una enzima hialuronidasa insertada en su genoma. Este adenovirus se distribuye más eficientemente por la masa tumoral y por consiguiente se aumenta el efecto oncolítico. Inyectando el adenovirus oncolítico de la invención endovenosamente se obtienen regresiones del volumen tumoral. Por lo tanto el adenovirus oncolítico de la presente invención es útil para el tratamiento del cáncer o de un estado pre-maligno del mismo.
Claims (2)
- REIVINDICACIONES1OFICINA ES ANOLA DE ATENTES Y MARCASN.° solicitud:ES ANAFecha de presentaci6n de la solicitud: 6. .3 Fecha de prioridad:INFORME SOBRE EL ESTADO DE LA TECNICAInt. Cl. : C12N151861 ( 6. ) A61K48100 ( 6. )DOCUMENTOS RELEVANTES
- Categoria
- ® Documentos citados Reivindicaciones afectadas
- Y Y Y Y Y GANESH S. et al.: "Relaxin� espressing fiber chimeric oncolytic adenovirus prolongs survival of tumor�bearingmice', CANCER RES, ( 7), vol. 67, no. , 7, paginas 43 �44 7, todo el documento. KIM JO O�HANG et al .: "Relaxin e xpression f rom t umor�targeting ade noviruses and its intratumoral spread, apoptosis induction, and efficacy", JOURNAL OF THE NATIONAL CANCER INSTITUTE, OXFORD UNIVERSITY RESS, GB, ( 6), vol 8, n° , pag. 48 � 4 3, todo el documento. GANESH S.: "Intratumoral coadministration of hyaluronidase enzyme and oncolytic adenoviruses enhances virus potency in metastatic tumor models", ( 8), CLINICAL CANCER RESEARCH, THE AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 4, n° , pag. 3 33� 3 4 , todo el documento. JIN CHENG et al.: "Human Matrix Metalloproteinase 8 Gene Delivery increases the Oncolytic Activityof a Replicating Adenovirus", ( 7), MOLECULAR THERA Y, vol. �, n° , pag. 8 � , todo el documento. TOOLE B et al.: "Hyaluronan; A constitutive regulator of chemoresistance and malignancyin cancer cells", SEMINARS IN CANCER BIOLOGY, SAUNDERS SCIENTIFIC UBLICATIONS, HILADEL HIA, A, US, ( 8), vol. 8, n° 4, pag. 44� � , todo el documento.
- Categoria de los documentos citados X: de particular relevancia Y: de particular relevancia combinado con otro/s de la misma categoria A: refleja el estado de la tecnica O: referido a divulgaci6n no escrita : publicado entre la fecha de prioridad yla de presentaci6n de la solicitud E: documento anterior, pero publicado despues de la fecha de presentaci6n de la solicitud
- El presente informe ha sido realizado � para todas las reivindicaciones � para las reivindicaciones n°:
- Fecha de realizaci6n del informe 3. 7. Examinador M. Hernandez Cuellar Pagina /4
INFORME DEL ESTADO DE LA TECNICAN° de solicitud:Documentaci6n minima buscada (sistema de clasificaci6n seguido de los simbolos de clasificaci6n) C N, A6 K Bases de datos electr6nicas consultadas durante la busqueda (nombre de la base de datos y, si es posible, terminos debusqueda utilizados) E ODOC, W I, MEDLINE, EMBASE, BIOSIS, CA LUSInforme del Estado de la Tecnica agina /4OPINION ESCRITAN° de solicitud:Fecha de Realizaci6n de la Opini6n Escrita: 3. 7.Declaraci6nNovedad (Art. .1 LP 11/198 ) Reivindicaciones SI Reivindicaciones NOActividad inventiva (Art. 8.1 LP11/198 ) Reivindicaciones SI Reivindicaciones NOSe considera que la solicitud cumple con el requisito de aplicaci6n industrial. Este requisito fue evaluado durante la fase de examen formal y tecnico de la solicitud (Articulo 3 . Ley / 86).Base de la Opini6n.-La presente opini6n se ha realizado sobre la base de la solicitud de patente tal y como se publica.Informe del Estado de la Tecnica agina 3/4OPINION ESCRITAN° de solicitud:1. Documentos considerados.-A continuaci6n se relacionan los documentos pertenecientes al estado de la tecnica tomados en consideraci6n para la realizaci6n de esta opini6n.- Documento
- Numero Publicaci6n o Identificaci6n Fecha Publicaci6n
- D
- GANESH S. et al.: "Relaxin� espressing fiber chimeric oncolytic adenovirus prolongs survival of tumor �bearing mice', CANCER RES, ( 7), vol. 67, n o. , 7, paginas 43 �44 7, todo el documento.
- D
- KIM JOO�HANG et al.: "Relaxin expression from tumor�targeting adenoviruses and i ts intratumoral sp read, apoptosis induction, and ef ficacy", JO URNAL O F THE NATIONAL CA NCER INSTITUTE, OXFORD UNIVERSITY RESS, GB, ( 6), vol 8, n° , pag. 48 � 4 3, todo el documento.
- D 3
- GANESH S.: "Intratumoral coadministration of hyaluronidase enzyme an d oncolytic adenoviruses enhances virus potency i n metastatic tumor m odels", ( 8), C LINICAL CANCER RESEARCH, THE AMERICAN ASSOCIATION FOR CANCER RESEARCH, US, vol. 4, n° , pag. 3 33� 3 4 , todo el documento.
- D 4
- JIN CHE NG et al .: "H uman Ma trix Metalloproteinase�8 Gene Delivery i ncreases the O ncolytic Activity of a R eplicating Adenovirus", ( 7), MO LECULAR T HERA Y, vol. �, n° , pag. 8 � , todo el documento.
- D �
- TOOLE B et al.: "Hyaluronan; A constitutive regulator of chemoresistance and malignancy in cancer cells", SEMINARS IN CANCER BIOLOGY, SAUNDERS SCIENTIFIC UBLICATIONS, HILADEL HIA, A, US, ( 8), vol. 8, n° 4, pag. 44�� , todo el documento.
- 2. Declaraci6n motivada segun los articulos 29. y 29.7 del Reglamento de ejecuci6n de la Ley 11/198 , de 20 de marzo, de Patentes sobre la novedad y la actividad inventiva; citas y explicaciones en apoyo de esta declaraci6nLa presente invenci6n se refiere a adenovirus oncoliticos que tienen una secuencia que codifica una hialuronidasa insertada en su genoma, asi como a composiciones farmaceuticas que comprenden el citado adenovirus y su uso para la fabricaci6n de un medicamento para el tratamiento del cancer..� NOVEDAD Ninguno de los documentos citados describe adenovirus oncoliticos que tienen una secuencia que codifica una hialuronidasa insertada e n s u ge noma. E n co nsecuencia l as reivindicaciones cumplen e l r equisito de nov edad establecido en el Art. 6. L / 86..�ACTIVIDAD INVENTIVA Cualquiera de los documentos D y D se puede considerar representativo del estado de la tecnica mas cercano a la invenci6n. Ambos documentos describen un adenovirus oncolitico que comprende una secuencia que codifica relaxina insertada en su genoma. La diferencia entre la informaci6n aportada en ambos documentos y la reivindicaci6n es la elecci6n de la hialuronidasa como el gen expresado por el adenovirus oncolitico. El efecto de esta diferencia es el mismoque el mostrado en ambos documentos, es decir, la degradaci6n de la matriz extracelular de las celulas tumorales para facilitar la diseminaci6n del adenovirus y mejorar su eficacia. El problema subyacente de la reivindicaci6n se puede plantear como la provisi6n de un adenovirus oncolitico alternativo con el mismo prop6sito. La soluci6n que proporciona la reivindicaci6n es un adenovirus oncolitico que tienen una secuencia que codifica una hialuronidasa insertada en su genoma. El documento D � describe la capacidad de la hialuronidasa para degradar la matriz extracelular de las celulas tumorales y permitir una diseminaci6n eficiente de los adenovirus oncoliticos que mejora la actividad anti tumoral, tal y como se describe en D 3. En este sentido se considera que la capacidad de degradar la matriz extracelular asi como su posible uso para mejorar la diseminaci6n y eficacia de un adenovirus oncolitico era informaci6n accesible para un experto en la materia con anterioridad la presentaci6n de la solicitud de patente. A la vista de la mejora proporcionada por la expresi6n de una enzima que degrada la matriz extracelular por el adenovirus oncolitico en vez de la coadministraci6n de la hialuronidasa con el adenovirus oncolitico, el experto en la materia habria conseguido el objeto de la reivindicaci6n sin esfuerzo inventivo. Las reivindicaciones dependientes tambien carecen de actividad inventiva ya que corresponden a realizaciones que se consideran rutinarias en el estado de la tecnica. Finalmente, losadenovirus oncoliticos descritos en el estado de la tecnica se usan para el tratamiento del cancer. En este sentido, los usos terapeuticos de las reivindicaciones y tambien carecen de actividad inventiva. En consecuencia, las reivindicaciones no cumplen el requisito establecido en el Art. 8. L / 86.Informe del Estado de la Tecnica agina 4/4
Priority Applications (20)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES200901201A ES2385251B1 (es) | 2009-05-06 | 2009-05-06 | Adenovirus oncolíticos para el tratamiento del cáncer. |
| RU2011149458/10A RU2536931C2 (ru) | 2009-05-06 | 2010-05-05 | Онколитический аденовирус для лечения рака, его применение и фармацевтическая композиция, содержащая его |
| US13/318,876 US10316065B2 (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
| PCT/ES2010/000196 WO2010128182A1 (es) | 2009-05-06 | 2010-05-05 | Adenovirus oncolíticos para el tratamiento del cáncer |
| PL10772050.0T PL2428229T5 (pl) | 2009-05-06 | 2010-05-05 | Onkolityczne adenowirusy do leczenia raka |
| JP2012509064A JP2012525833A (ja) | 2009-05-06 | 2010-05-05 | 癌治療のための腫瘍溶解アデノウイルス |
| EP10772050.0A EP2428229B2 (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
| MX2011011818A MX2011011818A (es) | 2009-05-06 | 2010-05-05 | Adenovirus oncoliticos para el tratamiento del cancer. |
| CN201710271203.8A CN107252438A (zh) | 2009-05-06 | 2010-05-05 | 用于治疗癌症的溶瘤腺病毒 |
| CN201080028895XA CN102548584A (zh) | 2009-05-06 | 2010-05-05 | 用于治疗癌症的溶瘤腺病毒 |
| CA2761183A CA2761183C (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
| KR1020117029097A KR101878274B1 (ko) | 2009-05-06 | 2010-05-05 | 암 치료용 암 용해성 아데노바이러스 |
| BRPI1011445A BRPI1011445B8 (pt) | 2009-05-06 | 2010-05-05 | Adenovírus oncolíticos para o tratamento de câncer |
| AU2010244348A AU2010244348B2 (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
| HK12108533.3A HK1167818B (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
| ES10772050T ES2600955T5 (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
| FIEP10772050.0T FI2428229T4 (fi) | 2009-05-06 | 2010-05-05 | Onkolyyttisiä adenoviruksia syövän hoitoon |
| HK18104062.5A HK1244679A1 (zh) | 2009-05-06 | 2018-03-23 | 用於治疗癌症的溶瘤腺病毒 |
| US16/405,285 US12129280B2 (en) | 2009-05-06 | 2019-05-07 | Oncolytic adenoviruses for treating cancer |
| US18/774,209 US20250011373A1 (en) | 2009-05-06 | 2024-07-16 | Oncolytic adenoviruses for treating cancer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES200901201A ES2385251B1 (es) | 2009-05-06 | 2009-05-06 | Adenovirus oncolíticos para el tratamiento del cáncer. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2385251A1 true ES2385251A1 (es) | 2012-07-20 |
| ES2385251B1 ES2385251B1 (es) | 2013-05-06 |
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES200901201A Expired - Fee Related ES2385251B1 (es) | 2009-05-06 | 2009-05-06 | Adenovirus oncolíticos para el tratamiento del cáncer. |
| ES10772050T Active ES2600955T5 (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES10772050T Active ES2600955T5 (en) | 2009-05-06 | 2010-05-05 | Oncolytic adenoviruses for treating cancer |
Country Status (15)
| Country | Link |
|---|---|
| US (3) | US10316065B2 (es) |
| EP (1) | EP2428229B2 (es) |
| JP (1) | JP2012525833A (es) |
| KR (1) | KR101878274B1 (es) |
| CN (2) | CN102548584A (es) |
| AU (1) | AU2010244348B2 (es) |
| BR (1) | BRPI1011445B8 (es) |
| CA (1) | CA2761183C (es) |
| ES (2) | ES2385251B1 (es) |
| FI (1) | FI2428229T4 (es) |
| HK (1) | HK1244679A1 (es) |
| MX (1) | MX2011011818A (es) |
| PL (1) | PL2428229T5 (es) |
| RU (1) | RU2536931C2 (es) |
| WO (1) | WO2010128182A1 (es) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ542873A (en) | 2003-03-05 | 2008-07-31 | Halozyme Inc | Soluble, neutral-active hyaluronidase activity glycoprotein (sHASEGP) that is produced with high yield in a mammalian expression system by introducing nucleic acids that lack a narrow region encoding amino acids in the carboxy terminus of the human PH20 cDNA |
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| WO2010128182A1 (es) | 2010-11-11 |
| BRPI1011445A2 (pt) | 2020-09-15 |
| CA2761183C (en) | 2019-03-26 |
| CN102548584A (zh) | 2012-07-04 |
| EP2428229B2 (en) | 2025-05-21 |
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| JP2012525833A (ja) | 2012-10-25 |
| ES2385251B1 (es) | 2013-05-06 |
| US20250011373A1 (en) | 2025-01-09 |
| AU2010244348B2 (en) | 2016-08-11 |
| BRPI1011445B8 (pt) | 2022-10-25 |
| PL2428229T3 (pl) | 2017-02-28 |
| PL2428229T5 (pl) | 2025-08-18 |
| KR101878274B1 (ko) | 2018-07-13 |
| CA2761183A1 (en) | 2010-11-11 |
| US20190345204A1 (en) | 2019-11-14 |
| RU2011149458A (ru) | 2013-06-27 |
| FI2428229T4 (fi) | 2025-07-29 |
| HK1167818A1 (en) | 2012-12-14 |
| EP2428229A1 (en) | 2012-03-14 |
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| RU2536931C2 (ru) | 2014-12-27 |
| US20120148535A1 (en) | 2012-06-14 |
| BRPI1011445B1 (pt) | 2022-10-04 |
| HK1244679A1 (zh) | 2018-08-17 |
| CN107252438A (zh) | 2017-10-17 |
| MX2011011818A (es) | 2012-06-19 |
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