Propanc Biopharma’s CEO Expresses Concern Over Disruption to Cancer Care During Global Pandemic
Propanc Biopharma (OTCQB: PPCB) highlights the disruptions in cancer care due to the global pandemic, emphasizing the increased risk of infection for patients. The company aims to advance its lead product candidate, PRP, which targets metastatic cancer without severe side effects or immune suppression. A study indicates that 42% of cancer patients faced treatment disruptions during COVID-19. Propanc is committed to developing effective therapies that enhance patient quality of life amidst these challenges.
- Company's lead product candidate PRP shows limited side effects and does not suppress immune function.
- PRP is designed to improve treatment outcomes without causing prolonged hospitalization.
- Disruptions in cancer care during the pandemic have affected patient access to treatments and clinical trials.
- Healthcare workers reported a 50% reduction in patient access to research and clinical trials.
Patients Experiencing Delays to Diagnoses and Treatment, to Halting Clinical Trials, and at High Risk of Infection During Treatment
A recent study in
In addition, people with cancer and their families experience greater uncertainty about their future, which may be further exacerbated by concerns about contracting the virus. For immune suppressed patients this is potentially life threatening. Sadly, infectious diseases remain a major cause of morbidity and mortality among cancer patients. Cancer can affect the immune system, increasing the risk of infection. In addition to cancer, infection can also be a primary cause of death in patients where cytotoxic chemotherapy produces severe and long-term neutropenia (too few neutrophils, an important type of white blood cell to fight infection), which may require hospitalization and lead to fatal infection. A research article published in the Biomed Central journal (BMC) by Elhadi, Khaled and Msherghi, 2021, focusing on infectious diseases as a cause of death among cancer patients in the US, concluded that timely intervention may help mitigate negative consequences on patients’ quality of life and prognosis.
“The global pandemic has highlighted a pressing need to provide better access to timely healthcare with effective, yet less toxic treatments that can improve quality of life for cancer patients,” said
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, which 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 it is unable to repay in cash; the Company’s ability to successfully 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; the Company’s ability to successfully initiate and complete clinical trials and its ability to successful 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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