Literature DB >> 11892945

ONYX-015. Onyx Pharmaceuticals.

E E Cohen1, C M Rudin.   

Abstract

ONYX-015 (CI-1042), an adenovirus modified selectively to replicate in and kill cells that harbor p53 mutations, is under development by Onyx Pharmaceuticals for the potential treatment of various solid tumors, including head and neck, gastrointestinal and pancreatic tumors. It is a recombinant adenovirus that carries a loss-of-function mutation at the E1B locus, the product of which is a 55 kDa protein that binds to and inactivates the p53 tumor suppressor protein. Wild-type adenoviruses must disable this gene before viral replication can occur. This, the ONYX-015 adenovirus will leave normal cells unaffected. Mutations in the p53 tumor suppressor gene are the most common type of genetic abnormality in cancer, occurring in more than half of all major cancer types. Thus, these cells are susceptible to the virus, which will readily replicate and cause cell death. ONYX-015 is in ongoing phase III trials for the treatment of recurrent head and neck cancer, phase II trials for colorectal, ovary, pancreas and mouth tumors, and phase I trials for digestive disease, esophagus and liver tumors. Onyx Pharmaceuticals was granted US-05677178 covering methods for the treatment of p53-related cancers in October 1997. The patent specifically covers the use of modified adenoviruses and other DNA viruses, which lack viral proteins that bind to p53, for the treatment of cancer patients whose tumors lack p53 function. The USPTO awarded Onyx Pharmaceuticals US-05846945 in December 1998, covering methods for treating cancer using replicating adenoviral therapy in combination with chemotherapy. In April 1999, the company also received EP-094910177.8 covering the technology in Europe.

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Year:  2001        PMID: 11892945

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  7 in total

Review 1.  Evolving lessons on nanomaterial-coated viral vectors for local and systemic gene therapy.

Authors:  Dayananda Kasala; A-Rum Yoon; Jinwoo Hong; Sung Wan Kim; Chae-Ok Yun
Journal:  Nanomedicine (Lond)       Date:  2016-06-27       Impact factor: 5.307

2.  An attenuated adenovirus, ONYX-015, as mouthwash therapy for premalignant oral dysplasia.

Authors:  Charles M Rudin; Ezra E W Cohen; Vassiliki A Papadimitrakopoulou; Sol Silverman; Wendy Recant; Adel K El-Naggar; Kirsten Stenson; Scott M Lippman; Waun Ki Hong; Everett E Vokes
Journal:  J Clin Oncol       Date:  2003-11-03       Impact factor: 44.544

3.  ONYX-411, a conditionally replicative oncolytic adenovirus, induces cell death in anaplastic thyroid carcinoma cell lines and suppresses the growth of xenograft tumors in nude mice.

Authors:  H V Reddi; P Madde; A J Reichert-Eberhardt; E C Galanis; J A Copland; B McIver; S K G Grebe; N L Eberhardt
Journal:  Cancer Gene Ther       Date:  2008-06-27       Impact factor: 5.987

Review 4.  Novel therapeutic strategies in prostate cancer management using gene therapy in combination with radiation therapy.

Authors:  Spencer J Collis; Kevin Khater; Theodore L DeWeese
Journal:  World J Urol       Date:  2003-08-13       Impact factor: 3.661

Review 5.  Immuno- and gene-therapeutic strategies targeted against cancer (mainly focusing on pancreatic cancer).

Authors:  Kiyoshi Yoshimura; Kelly Olino; Barish H Edil; Richard D Schulick; Masaaki Oka
Journal:  Surg Today       Date:  2010-04-28       Impact factor: 2.540

6.  Heat shock protein 72 expression allows permissive replication of oncolytic adenovirus dl1520 (ONYX-015) in rat glioblastoma cells.

Authors:  Jonathan Madara; James A Krewet; Maulik Shah
Journal:  Mol Cancer       Date:  2005-03-11       Impact factor: 27.401

Review 7.  Chemoprevention of Head and Neck Cancers: Does It Have Only One Face?

Authors:  Krzysztof Siemianowicz; Wirginia Likus; Mariola Dorecka; Renata Wilk; Włodzimierz Dziubdziela; Jarosław Markowski
Journal:  Biomed Res Int       Date:  2018-09-25       Impact factor: 3.411

  7 in total

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