Posts Tagged ‘Cancer treatment’

ASX Company News: Bionomics Granted Cancer Treatment US Patent

Thursday, August 16th, 2012

Bionomics Limited (BNO) has been granted its key patent (US 8,198,466) relating to its vascular disrupting agent BNC105 by the United States Patent and Trademark Office. This patent is at the centre of the BNC105 patent portfolio. The patent is valid for 20 years to February 2027. BNC105 patents have been filed in each of the major pharmaceutical markets. Granting of this patent has already occurred in Australia and New Zealand.

CEO and Managing Director of Bionomics Dr Deborah Rathjen said the granting of this patent in the US is a milestone in Bionomics’ patent strategy for the BNC105 program. “This solidifies our intellectual property protection for Bionomics’ lead oncology clinical stage asset. The granted patent provides a substantial value-add for the BNC105 program and strengthens our partnering data package.” Bionomics has also filed a patent application for the manufacture of BNC105. Bionomics owns additional patents and has applications covering vascular disrupting agents related to BNC105, together with methods of treatment of cancer both as monotherapy and in combination with selected therapies.

Bionomics (BNO) is a leading international biotechnology company which discovers and develops innovative therapeutics for cancer and diseases of the central nervous system. Bionomics has small molecule product development programs in the areas of cancer, anxiety, Alzheimer’s disease, epilepsy and multiple sclerosis.BNC105, which is undergoing clinical development for the treatment of cancer, is based upon the identification of a novel compound that potently and selectively restricts blood flow within tumours. Bionomics’ discovery and development activities are driven by its three technology platforms: Angene®, a drug discovery platform which incorporates a variety of genomics tools to identify and validate novel angiogenesis targets (involved in the formation of new blood vessels). MultiCore® is Bionomics’ proprietary, diversity orientated chemistry platform for the discovery of small molecule drugs. ionX® is a set of novel technologies for the identification of drugs targeting ion channels for diseases of the central nervous system.

www.bionomics.com.au

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ASX Company News: Novogen Acquires S*BIO’s HDAC Inhibitor

Friday, August 10th, 2012

Novogen’s (NRT) subsidiary, MEI Pharma, Inc., an oncology company focused on the clinical development of novel therapies for the treatment of cancer, announced that it has entered into a definitive asset purchase agreement with S*BIO Pte Ltd, a privately held biotechnology company, pursuant to which MEI Pharma will acquire S*BIO’s exclusive worldwide rights to Pracinostat, an investigational, potential best-in-class, oral histone deacetylase (HDAC) inhibitor.

“We are excited to seize this opportunity to bolster our pipeline with a potential best-in-class, late-stage compound with activity against a validated target, under favourable terms,” said Daniel P Gold, PhD, President and Chief Executive Officer of MEI Pharma. “The acquisition of Pracinostat broadens our potential addressable market in oncology with applications in both hematologic disorders and solid tumours. We believe that the addition of this targeted small molecule to our existing portfolio of novel isoflavone-based drug candidates, ME-143 and ME-344, will significantly enhance shareholder value.”

Pracinostat is a selective inhibitor of a group of enzymes called histone deacetylases (HDAC).  HDACs belong to a larger set of proteins collectively known as epigenetic regulators that can alter gene expression by chemically modifying DNA or its associated chromosomal proteins. Abnormal activity of these regulators is believed to play an important role in cancer and other diseases.

There are currently two HDAC inhibitors approved by the U.S. Food and Drug Administration (FDA) for the treatment of cutaneous T-cell lymphoma, one of which is also approved for the treatment of peripheral T-cell lymphoma. Pracinostat has been generally well tolerated in clinical testing of more than 150 patients, with readily manageable side effects often associated with drugs of this class. The most common adverse event (all grades) is fatigue. Data from a Phase II clinical trial of oral Pracinostat showed evidence of single-agent activity in heavily pre-treated patients with intermediate or high-risk myelofibrosis, with two patients showing a clinical improvement. These results are scheduled for publication in the September, 2012 issue of Leukemia Research.

www.novogen.com

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ASX Company News: Viralytics Japanese Patent Granted

Friday, August 10th, 2012

Viralytics Limited (VLA) is pleased to announce that it has received notice of a decision to grant a patent in Japan involving the use of Coxsackie A viruses including CAVATAKTM in the treatment of multiple myeloma. Japan is the world’s third largest pharmaceutical market behind the US and Europe, and multiple myeloma is an important blood cancer for which the patient prognosis is exceptionally poor, so the medical need is large. Specifically the patent covers the use of a pharmaceutical composition of any of the Coxsackieviruses A13, A15, A18, A20 and A21 in treating multiple myeloma. CAVATAKTM is Coxsackievirus A21.

Viralytics is listed on the Australian Stock Exchange (VLA), Viralytics’ principal asset is the intellectual property relating to CAVATAKTM, an Oncolytic Virus technology. CAVATAKTM is the trade name for Viralytics’ proprietary formulation of the Coxsackievirus Type A21 (CVA21). EVATAKTM is the trade name for Viralytics’ proprietary formulation of the Echovirus Type 1 (EV1). CVA21 and EV1 are viruses that occur naturally in the community. CVA21 and EV1 attach to the outside of  cells, using a specific ‘receptor’ on the cell’s surface (like a key fitting a lock). CVA21 uses the receptors, intercellular adhesion

www.viralytics.com

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ASX Company News: Viralytics Granted Cancer Virus Patent

Friday, August 3rd, 2012

Viralytics Limited (VLA) is pleased to announce the granting of a notice of allowance by the United States Patent and Trademark Office (USPTO) of a patent around CAVATAKTM, Viralytics’ Phase II cancer drug based on Coxsackievirus A21. The USPTO has advised Viralytics that the patent will grant on August 7, 2012 being identified as US Patent No. 8,236,298. Specifically, the claims in the notice of allowance cover the use of Picornaviruses (a large family of viruses including Coxsackievirus A21) to destroy cancerous blood cells in stem cell grafts prior to transplantation.

Dr Darren Shafren, Viralytics Chief Scientific Officer said “the use of Picornaviruses, including CAVATAKTM to target and destroy cancerous cells in stem cell transplants used in treatment of blood cancer is a new and exciting application of Viralytics’ oncolytic viruses. Our current clinical strategy for CAVATAKTM is to focus on both intratumoural (injecting directly into the tumour) and intravenous (via the bloodstream) routes of delivery.

Viralytics is listed on the Australian Stock Exchange (VLA), Viralytics ADR trades under VRACY on the OTC market in the USA. Viralytics’ principal asset is the intellectual property relating to CAVATAKTM, an Oncolytic Virus technology.

www.viralytics.com

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ASX Company News: Novogen Subsidiary Granted US Patent

Friday, April 27th, 2012

Novogen (NRT) subsidiary, Marshall Edwards, Inc.,  an oncology company focused on the clinical development of novel therapeutics targeting cancer metabolism, announced that the US Patent and Trademark Office has issued Patent No. 8,163,795 covering the company’s lead drug candidate ME-143 for use in treating cancer. The patent is expected to provide protection until September 2025. The company also announced that it has received notices of allowance from the Japanese Patent Office for two patents that cover the ME-143 and ME-344 compositions of matter, respectively, and their use in treating cancer.

“This key US patent for ME-143 follows on the heels of a related patent for ME-344 as well as a composition patent for both compounds, solidifying the intellectual property position surrounding our two lead oncology drug candidates,” said Daniel P Gold PhD, President and Chief Executive Officer of Marshall Edwards. “As we prepare for our upcoming Phase II clinical trials, we believe our strong patent estate will help to facilitate our partnering efforts both in the US and in high growth markets abroad.”

Marshall Edwards owns exclusive worldwide rights to all of its drug candidates, including ME-143 and ME-344. The company’s intellectual property portfolio now includes 15 issued US patents, at least 12 additional US patent applications, and more than 70 issued foreign patents and 50 foreign patent applications. Marshall Edwards, Inc. is a San Diego-based oncology company focused on the clinical development of novel therapeutics targeting cancer metabolism. Novogen Limited (NRT) is an Australian biotechnology company based in Sydney, Australia. Novogen conducts research and development on oncology therapeutics through its subsidiary, Marshall Edwards, Inc., and is developing glucan technology through its subsidiary, Glycotex, Inc.

www.novogen.com

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ASX Company News: Prima BioMed Granted Ovarian Cancer Patent

Thursday, April 12th, 2012

Australian cancer treatment development company Prima BioMed Ltd (PRR) is pleased to announce that it has received Notification of Grant by the Canadian Patent Office for its ovarian cancer vaccine, CvacTM. Patent number 2304952 is titled, “Mannose receptor bearing cell line and antigen composition” and expires on 29 September 2018. The patent has also been granted in Australia, Europe, and Japan. The granted patent claims are method of composition and protect the formulation of Prima’s autologous dendritic cell vaccine CVacTM. CVacTM is composed of a patients’ own dendritic cells pulsed with the cancer antigen Mucin-1, conjugated to oxidised mannan fusion protein. The pulsed dendritic cells are then reinjected into the patient to stimulate an immune response to the Mucin-1 cancer antigen.

CVacTM is Prima BioMed’s lead development product. It is a vaccine therapy treatment for ovarian cancer sufferers that is administered post-surgery and post-chemotherapy to attempt to delay the relapse and control metastases. There is a large un-met medical need for new treatments for ovarian cancer which has a very high morbidity rate. There are currently no maintenance-based therapy products commercially available for this disease.

Prima BioMed is an ASX listed Australian health care company. The Company is focused on technologies in the fields of cancer immunotherapy and immunology. Prima’s lead product is CVacTM ovarian cancer therapy treatment.

www.primabiomed.com.au

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ASX Company News: Viralytics Granted Chinese Blood Cancer Patent

Friday, March 30th, 2012

Viralytics Limited (VLA) is pleased to announce the receipt of a notice to grant a patent in China involving the use of a panel of Coxsackie A viruses including CAVATAKTM in the treatment of the blood cancer, multiple myeloma. The scope of this application covers the use of Coxsackieviruses A13, A15, A18 and A21 (CAVATAKTM) in the manufacture of a medication for treating multiple myeloma. Furthermore, the application covers the use of the above listed Coxsackie A viruses in the laboratory removal of malignant multiple myeloma cells within auto grafts prior to autologous stem cell transplantation. Multiple myeloma is a type of cancer that begins in white blood cells that produce antibodies. Approximately 22,000 new cases and 11,000 deaths are expected from multiple myeloma within the US in 2012. CAVATAKTM is currently being evaluated in a US Phase II clinical trial in late stage melanoma patients, under an Investigational New Drug application allowed by the US Food and Drug Administration.

Viralytics’ (VLA), principal asset is the intellectual property relating to CAVATAKTM, an Oncolytic Virus technology. CAVATAKTM is the trade name for Viralytics’ proprietary formulation of the Coxsackievirus Type A21 (CVA21). EVATAKTM is the trade name for Viralytics’ proprietary formulation of the Echovirus Type 1 (EV1). CVA21 and EV1 are viruses that occur naturally in the community. CVA21 and EV1 attach to the outside of cells, using a specific ‘receptor’ on the cell’s surface (like a key fitting a lock). CVA21 uses the receptors, intercellular adhesion molecule-1 (ICAM-1) and/or decay accelerating factor (DAF) to bind and infect target cells. Both of these receptor proteins have been demonstrated to be highly expressed on multiple cancer types, including: melanoma, prostate cancer, breast cancer, multiple myeloma and others. EV1 uses the receptor, integrin α2β1 (alpha 2 beta 1) receptorto bind and infect target cells.

www.viralytics.com

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ASX Company News: Viralytics Granted Cancer Virus Patent

Thursday, February 16th, 2012

Viralytics Limited (VLA) is pleased to announce the granting of a patent by the United States Patent and Trademark Office covering a Coxsackie A virus capable of infecting cancer cells substantially in the absence of intercellular adhesion molecule-1 (ICAM-1).

Dr Darren Shafren, Viralytics Chief Scientific Officer said “CAVATAKTM targets and destroys cancerous cells following binding to surface expressed ICAM-1. The generation of this novel Coxsackie A virus, that can infect cancer cells in the absence of ICAM-1 expands the range of cancers that Viralytics panel of oncolytic viruses can potentially target”.

The scope of the allowed claims of Patent No. 8,114,416 covers a bio- selected form of Coxsackievirus A21 which was generated following passage in cells not expressing ICAM-1 but expressing decay accelerating factor  (DAF). Decay accelerating factor expression is up-regulated on the surface of many cancerous cells including ovarian, colorectal and gastric cancers,

making it a target for the newly bio-selected Coxsackievirus A21. Claims of the patent also cover specific changes induced on the surface of the Coxsackievirus A21 during the bio-selection process on DAF-expressing cancer cells that are believed to confer the extended scope of cancer cell targeting.

Viralytics’ principal asset is the intellectual property relating to CAVATAKTM, an Oncolytic Virus technology. CAVATAKTM is the trade name for Viralytics’ proprietary formulation of the Coxsackievirus Type A21 (CVA21). EVATAKTM is the trade name for Viralytics’ proprietary formulation of the Echovirus Type 1 (EV1). CVA21 and EV1 are viruses that occur naturally in the community. CVA21 and EV1 attach to the outside of cells, using a specific ‘receptor’ on the cell’s surface (like a key fitting a lock). CVA21 uses the receptors, intercellular adhesion molecule-1 (ICAM-1) and/or decay accelerating factor (DAF) to bind and infect target cells. Both of these receptor proteins have been demonstrated to be highly expressed on multiple cancer types, including: melanoma, prostate cancer, breast cancer, multiple myeloma and others. EV1 uses the receptor, integrin α2β1 to bind and infect target cells. Integrin α2β1 has been demonstrated to be highly expressed on multiple cancer types, including: prostate cancer, ovarian cancer and others.

www.viralytics.com

http://www.traderdealer.com.au/fundamentals/vla

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ASX Company News: Novogen Secures Cancer Treatment Patent

Thursday, December 22nd, 2011

Novogen (NRT) subsidiary, Marshall Edwards, Inc., an oncology company focused on the clinical development of novel therapeutics targeting cancer metabolism, announced today that the US Patent and Trademark Office has issued a new patent covering a number of the company’s isoflavone-based compounds, including lead oncology drug candidates ME-143 and ME-344, and their pharmaceutical compositions. The patent is estimated to provide protection until March 2027.

“This patent represents another important milestone in our efforts to develop our lead drug candidates into valuable treatment options for patients with cancer” said Daniel P Gold, PhD, President and Chief Executive Officer of Marshall Edwards. “Furthermore, this demonstrates our commitment to further strengthening the intellectual property portfolio we acquired earlier this year, which will be essential for partnering any of our drug candidates and enhancing shareholder value.”

Marshall Edwards completed the acquisition of its isoflavone-based intellectual property portfolio, including worldwide rights to lead oncology drug candidates ME-143 and ME-344, from Novogen Limited in May 2011. The portfolio now includes 11 issued US patents, at least 14 US patent applications, at least 40 issued foreign patents and at least 80 foreign patent applications. Marshall Edwards, Inc. is a San Diego-based oncology company focused on the clinical development of novel anti-cancer therapeutics. The company’s lead programs focus on two families of small molecules that result in the inhibition of tumour cell metabolism. Novogen Limited (NRT) is an Australian biotechnology company based in Sydney, Australia. Novogen conducts research and development on oncology therapeutics through its subsidiary, Marshall Edwards, Inc., and is developing glucan technology through its subsidiary, Glycotex, Inc.

www.novogen.com

http://www.traderdealer.com.au/Fundamentals/nrt

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ASX Company News: Viralytics Granted US Cancer Treatment Patent

Monday, November 28th, 2011

Viralytics Ltd (VLA) is pleased to announce the granting of a notice of allowance by the United States Patent and Trademark Office for issuance of a patent covering a Coxsackie A virus capable of infecting cancer cells substantially in the absence of intercellular adhesion molecule-1 (ICAM-1).  Dr Darren Shafren, Viralytics Chief Scientific Officer said “CAVATAK  targets and destroys cancerous cells following binding to surface expressed ICAM-1. The generation of this novel Coxsackie A virus, that can infect cancer cells in the absence of ICAM-1 expands the range of cancers that Viralytics panel of oncolytic viruses can potentially target”.

The scope of the allowed claims of US 10/592,395 covers a bio-selected form of Coxsackievirus A21 which was generated following passage in cells not expressing ICAM-1 but expressing decay accelerating factor (DAF). Decay accelerating factor expression is up-regulated on the surface of many cancerous cells including ovarian, colo-rectal and gastric cancers, making it a target for the newly bio-selected Coxsackievirus A21. The allowed claims also cover specific changes induced on the surface of the Coxsackievirus A21 during the bio-selection process on DAF-expressing cancer cells that are believed to confer the extended scope of cancer cell targeting.

www.viralytics.com

http://www.traderdealer.com.au/fundamentals/vla

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