PharmaCyte Biotech to Present at H.C. Wainwright BioConnect Conference
PharmaCyte Biotech (NASDAQ: PMCB) announced its participation as a presenting company at the virtual H.C. Wainwright BioConnect Conference from January 10-13, 2022. CEO Kenneth L. Waggoner will discuss the company's business and product pipeline during the presentation, available on-demand starting January 10, 2022. Additionally, PharmaCyte plans to release an update on its clinical hold by the FDA for its Phase 2b trial targeting locally advanced pancreatic cancer. More information is available on their website.
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During the presentation, the Chief Executive Officer of
Over 500 corporate presentations and panels are available on-demand from
PharmaCyte’s presentation will also be available at https://journey.ct.events/view/e3f318a9-38db-4326-8ec0-682398bf4a50.
Additionally, PharmaCyte will be publishing a press release in the coming weeks to update its shareholders on the progress PharmaCyte has made to lift the clinical hold the
To learn more about PharmaCyte’s pancreatic cancer treatment and how it works inside the body to treat locally advanced, inoperable pancreatic cancer, we encourage you to watch PharmaCyte’s documentary video complete with medical animations at https://www.PharmaCyte.com/Cancer.
About
PharmaCyte’s therapy for cancer involves encapsulating genetically engineered human cells that convert an inactive chemotherapy drug into its active or “cancer-killing” form. For pancreatic cancer, these encapsulated cells are implanted in the blood supply to the patient’s tumor as close as possible to the site of the tumor. Once implanted, a chemotherapy drug that is normally activated in the liver (ifosfamide) is given intravenously at one-third the normal dose. The ifosfamide is carried by the circulatory system to where the encapsulated cells have been implanted. When the ifosfamide flows through pores in the capsules, the live cells inside act as a “bio-artificial liver” and activate the chemotherapy drug at the site of the cancer. This “targeted chemotherapy” has proven effective and safe to use in past clinical trials and we believe results in little to no treatment related side effects.
PharmaCyte’s therapy for Type 1 diabetes and insulin-dependent Type 2 diabetes involves encapsulating a human cell line that has been genetically engineered to produce and release insulin in response to the levels of blood sugar in the human body. The encapsulation of the cell line will be done using the Cell-in-a-Box technology. Once the encapsulated cells are implanted in a diabetic patient, we anticipate that they will function as a “bio-artificial pancreas” for purposes of insulin production.
Safe Harbor
This press release may contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that express the current beliefs and expectations of the management of PharmaCyte. Any statements contained herein that do not describe historical facts are forward-looking statements that are subject to risks and uncertainties that could cause actual results, performance, and achievements to differ materially from those discussed in such forward-looking statements. Factors that could affect our actual results include our ability to raise the necessary capital to fund our operations and to find partners to supplement our capabilities and resources, our ability to satisfactorily address the issues raised by the FDA in order to have the clinical hold on our IND removed, as well as such other factors that are included in the periodic reports on Form 10-K and Form 10-Q that we file with the
More information about
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Investor Relations:
Dr.
Telephone: 917.595.2856
Email: InvestorRelations@PharmaCyte.com
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