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Propanc Biopharma Receives Certificate of Grant for “Composition of Proenzymes for Cancer Treatment” Patent from European Patent Office

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Propanc Biopharma receives a certificate of grant for the 'Composition of Proenzymes for Cancer Treatment' patent from the European Patent Office. The patent covers lower dosage ratios of the two proenzymes in the PRP formulation, expanding the Company's IP portfolio to 94 patents filed globally. This development is important as the Company progresses into early-stage clinical trials, aiming to establish itself as a leader in cancer treatment innovation.
Positive
  • Propanc Biopharma receives a certificate of grant for the 'Composition of Proenzymes for Cancer Treatment' patent from the European Patent Office.
  • The patent covers lower dosage ratios of the two proenzymes in the PRP formulation.
  • The Company's IP portfolio will grow to 94 patents filed in major global jurisdictions.
  • The patent is essential for future clinical dosage ranges for PRP as the Company advances into early-stage clinical development.
  • Europe, where the patent is granted, accounted for 23.4% of global pharmaceutical sales in 2021.
  • The worldwide pharmaceutical market was valued at approximately $1.48 trillion in 2022.
  • The Company aims to protect its novel invention and create future value for shareholders with the growing IP portfolio.
  • Propanc Biopharma plans to advance PRP into the clinic, positioning itself as a pioneer in cancer treatment.
Negative
  • None.

MELBOURNE, Australia--(BUSINESS WIRE)-- Propanc Biopharma, Inc. (OTC Pink: PPCB) (“Propanc” or the “Company”), a biopharmaceutical company developing novel cancer treatments for patients suffering from recurring and metastatic cancer, today announced that a certificate of grant for the Company’s “composition of proenzymes for cancer treatment,” patent was received from the European Patent Office. The patent covers lower dosage ratios of the two proenzymes (trypsinogen and chymotrypsinogen) contained in the PRP formulation. This is the fourth European patent granted and after validation in selected countries across Europe, will result in the Company’s IP portfolio growing to 94 patents filed in major global jurisdictions.

This PRP dosing 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. Furthermore, Europe is considered a major global region which accounted for 23.4% of global pharmaceutical sales in 2021, according to the European Federation of Pharmaceutical Industries and Associations (EFPIA). This is a significant percentage when you consider that in 2022, the worldwide pharmaceutical market was valued at approximately $1.48 trillion by Statista.com.

“The PRP dosing patent at lower dosage ratios is an important part of our growing IP portfolio, as we seek to protect our novel invention and create future value for our shareholders,” said Mr. James Nathanielsz, Propanc’s Chief Executive Officer. “We look forward to advancing PRP into the clinic, and together with our growing IP portfolio, establishing the Company as a pioneer in the way we treat this killer disease.”

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.

Investor Relations and Media Contacts: 

James Nathanielsz

Propanc Biopharma, Inc.

irteam@propanc.com

+61-3-9882-0780

Source: Propanc Biopharma, Inc.

FAQ

What patent did Propanc Biopharma receive from the European Patent Office?

Propanc Biopharma received a certificate of grant for the 'Composition of Proenzymes for Cancer Treatment' patent from the European Patent Office.

What does the patent cover?

The patent covers lower dosage ratios of the two proenzymes (trypsinogen and chymotrypsinogen) contained in the PRP formulation.

How many patents will be in Propanc Biopharma's IP portfolio after this grant?

The Company's IP portfolio will grow to 94 patents filed in major global jurisdictions.

Why is the PRP dosing patent important for the Company?

The PRP dosing patent is important for future clinical dosage ranges for PRP as the Company advances into early-stage clinical development.

What percentage of global pharmaceutical sales did Europe account for in 2021?

Europe accounted for 23.4% of global pharmaceutical sales in 2021.

What was the value of the worldwide pharmaceutical market in 2022?

The worldwide pharmaceutical market was valued at approximately $1.48 trillion in 2022.

Who is the Chief Executive Officer of Propanc Biopharma?

Mr. James Nathanielsz is the Chief Executive Officer of Propanc Biopharma.

Propanc Biopharma, Inc.

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About PPCB

propanc biopharma, inc., a development-stage healthcare company, focuses on the development of cancer treatments for patients with pancreatic, ovarian, and colorectal cancer in australia. its lead product is prp, a formulation that is in preclinical phase of development designed to enhance the anti-cancer effects of multiple enzymes acting synergistically. the company has a research collaboration with university of jaã©n to commence the pop1 joint drug discovery program. the company was formerly known as propanc health group corporation and changed its name to propanc biopharma, inc. in april 2017. propanc biopharma, inc. was founded in 2007 and is based in camberwell, australia.