Propanc Biopharma Announces No Immediate Plans for Reverse Stock Split
Propanc Biopharma, Inc. filed a Definitive Information Statement under Section 14C of the Exchange Act on June 9, 2022, to increase authorized shares and allow for a potential reverse stock split at the board's discretion. CEO James Nathanielsz noted that this move is essential due to recent volatile market conditions impacting microcap companies. The company is committed to advancing its lead product candidate, PRP, which is designed to target various cancers, and is actively pursuing strategic partnerships for clinical development.
- Filed for an increase in authorized shares to adapt to market conditions.
- Continues to work on the development of PRP, a cancer treatment.
- Exploring strategic partnerships for advancing clinical research.
- The company is currently dependent on substantial debt financing that it cannot repay in cash.
- Uncertainties regarding the ability to complete clinical trials and develop PRP.
Company Filed a Definitive Information Statement Under Section 14C of the Exchange Act
“Volatile market conditions as a result of recent global events have meant that CEO’s of publicly listed Companies are navigating through unchartered waters.
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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