Propanc Biopharma’s Joint Researcher Presents at the 43rd Meeting of the European Organization of Research & Treatment of Cancer (EORTC)
Propanc Biopharma, Inc. (OTC Pink: PPCB) announced significant developments in cancer treatment at the 43rd EORTC PAMM meeting, where Mrs. Belén Toledo Cutillas presented novel strategies to disrupt tumor support systems. This approach aims to enhance drug efficacy against chemoresistant tumors. CEO James Nathanielsz emphasized PRP's prospective application as an adjunct therapy, targeting cancer stem cells. The global metastatic cancer market is forecasted at $111 Billion by 2027, highlighting the potential for Propanc's innovative research initiatives with Spanish universities.
- Successful presentation at EORTC conference indicating recognition within the scientific community.
- Highlighting PRP's potential to improve efficacy of current cancer treatments.
- Collaboration with Spanish universities enhances research capabilities and credibility.
- Forecast for the metastatic cancer market at $111 Billion by 2027 suggests significant market opportunity.
- None.
“Participation at the EORTC-PAMM meeting provided an opportunity to present our latest findings to scientific experts and clinical researchers looking for cutting-edge opportunities in cancer drug development. Our research highlights future potential clinical applications of our lead product candidate, PRP, as a pre-treatment with current standard treatment approaches and existing innovative cancer therapies,” said Mr.
The EORTC’s mission is to increase people’s survival and quality of life by testing new therapeutic strategies based on existing drugs, surgery and radiotherapy. The EORTC also helps develop new drugs and approaches in partnership with the pharmaceutical industry and in patients’ best interests. The EORTC research network consists of over 5,500 collaborators from all disciplines involved in cancer treatment and research in more than 930 institutions in 27 countries. Its research spans the entire spectrum from translational and pre-clinical research to large, prospective, multi-center, phase III clinical trials that evaluate new cancer therapies.
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 kidney, ovarian, breast, brain, prostate, colorectal, lung, liver, uterine, and skin cancers.
About
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.
To view the Company’s “Mechanism of Action” video on its anti-cancer lead product candidate, PRP, please click on the following link: http://www.propanc.com/news-media/video.
Forward-Looking Statements
All statements other than statements of historical facts contained in this press release are “forward-looking statements,” which may often, but not always, be identified by the use of such words as “may,” “might,” “will,” “will likely result,” “would,” “should,” “estimate,” “plan,” “project,” “forecast,” “intend,” “expect,” “anticipate,” “believe,” “seek,” “continue,” “target,” or the negative of such terms or other similar expressions. These statements involve known and unknown risks, uncertainties, and other factors, that may cause actual results, performance, or achievements to differ materially from those expressed or implied by such statements. These factors include uncertainties as to the Company’s ability to continue as a going concern absent new debt or equity financings; the Company’s current reliance on substantial debt financing that, as of the date of this press release, it would have substantial difficulty repaying in cash; the Company’s ability successfully to remediate material weaknesses in its internal controls; the Company’s ability to reach research and development milestones as planned and within proposed budgets; the Company’s ability to control costs; the Company’s ability to obtain adequate new financing on reasonable terms on an as-needed basis; the Company’s ability successfully to initiate and complete clinical trials and to develop PRP, its lead product candidate; the Company’s ability to obtain and maintain patent protection; the Company’s ability to recruit employees and directors with accounting and finance expertise; the Company’s dependence on third parties for services; the Company’s dependence on key executives; the impact of government regulations, including FDA regulations; the impact of any future litigation; the availability of capital; changes in economic conditions; competition; and other risks, including, but not limited to, those described in the Company’s periodic reports that are filed with the
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