Propanc Biopharma Receives Certificate of Grant for “Proenzymes Composition” Patent from Japanese Patent Office
Propanc Biopharma, a biopharmaceutical company, announced receiving a Certificate of Grant for its “proenzymes composition” patent from the Japanese Patent Office, marking its fourth Japanese patent. This patent covers dosing regimen claims for PRP, the company's lead asset, advancing to clinical development. Additionally, the Intellectual Property of Malaysia granted a patent for a cancer treatment using trypsinogen and chymotrypsinogen, the company's third patent in Malaysia. Propanc's intellectual property portfolio now includes 93 patents worldwide for using PRP against solid tumors. Japan's pharmaceutical market, projected to reach $46.36 billion in 2024, is a key market for Propanc. The company aims to advance PRP into a Phase 1b clinical study, targeting and eradicating cancer stem cells without severe side effects.
- Received Certificate of Grant for “proenzymes composition” patent from Japanese Patent Office.
- Received a Certificate of Grant from Intellectual Property of Malaysia for a cancer treatment patent.
- Expanded intellectual property portfolio to 93 patents worldwide.
- Japan's pharmaceutical market is projected to reach $46.36 billion in 2024, with a significant oncology sector.
- Plans to advance PRP into a Phase 1b clinical study.
- None.
Certificate of Grant Received for “Cancer Treatment” Patent from IP Corporation of
The proenzymes composition patent is an important part of the IP portfolio as it covers possible future clinical dosage ranges for PRP as the Company advances into early-stage clinical development.
The cancer treatment patent describes a method to target and eradicate cancer stem cells (CSCs) using PRP which minimizes the progression of cancer in a patient. Currently, progression, or spread of cancer, called metastatic cancer, is the main cause of patient death for sufferers.
“We are building an extensive and mature intellectual property portfolio around the use of proenzymes as a novel treatment for advanced solid tumors,” said Mr. James Nathanielsz, Propanc’s Chief Executive Officer. “We plan to grow our intellectual property portfolio by filing additional provisional patent applications, as we progress PRP into the clinic. Intellectual property protection is a cornerstone of our drug development strategy, as we seek to protect the tremendous value in our promising lead product candidate, PRP. We look forward to executing our plans to advance PRP into a Phase 1b clinical study in advanced cancer patients, as a novel therapy for the treatment and prevention of metastatic cancer from solid tumors by targeting and eradicating CSCs, but without the side effects normally associated with standard treatment approaches.”
About PRP:
PRP is a mixture of two proenzymes, trypsinogen and chymotrypsinogen from bovine pancreas, administered by intravenous injection. A synergistic ratio of 1:6 inhibits growth of most tumor cells. Examples include pancreatic, ovarian, kidney, breast, brain, prostate, colorectal, lung, liver, uterine, and skin cancers. Orphan Drug Designation status of PRP has been granted from the US Food and Drug Administration (FDA) for treatment of pancreatic cancer.
To view the Company’s “Mechanism of Action” video on the Company’s lead asset, PRP, please click on the following link: http://www.propanc.com/news-media/video.
About Propanc Biopharma, Inc.
Propanc Biopharma, Inc. (the “Company”) is developing a novel approach to prevent recurrence and metastasis of solid tumors by using pancreatic proenzymes that target and eradicate cancer stem cells in patients suffering from pancreatic, ovarian, and colorectal cancers. For more information, please visit www.propanc.com.
The Company’s novel proenzyme therapy is based on the science that enzymes stimulate biological reactions in the body, especially enzymes secreted by the pancreas. These pancreatic enzymes could represent the body’s primary defense against cancer.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements reflect management’s current expectations, as of the date of this press release, and involve certain risks and uncertainties. Forward-looking statements include statements herein with respect to the planned studies and market projections described above and the successful execution of the Company’s business strategy. The Company’s actual results could differ materially from those anticipated in these forward-looking statements because of various factors. Such risks and uncertainties include, among other things, our ability to establish and maintain the proprietary nature of our technology through the patent process; the availability of financing; the Company’s ability to implement its long range business plan for various applications of its technology; the Company’s ability to enter into agreements with any necessary business partners; the impact of competition; the obtaining and maintenance of any necessary regulatory clearances applicable to applications of the Company’s technology; and management of growth and other risks and uncertainties that may be detailed from time to time in the Company’s reports filed with the SEC.
View source version on businesswire.com: https://www.businesswire.com/news/home/20240625873108/en/
Investor Relations and Media Contacts:
James Nathanielsz
Propanc Biopharma, Inc.
irteam@propanc.com
+61-3-9882-0780
Source: Propanc Biopharma, Inc.
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