RenovoRx Announces Presentation at the 2022 SPECTRUM Conference Highlighting Its Innovative RenovoTAMP™ Therapy for Targeted Treatment of Cancer
RenovoRx, Inc. (Nasdaq: RNXT) presented its RenovoTAMP™ therapy platform at the 2022 SPECTRUM Conference in Miami. Dr. Ripal Gandhi, a Principal Investigator for the Phase 3 TIGeR-PaC clinical trial, highlighted data suggesting that RenovoTAMP, combined with radiation therapy, can significantly reduce systemic chemotherapy exposure and its associated side effects. The therapy aims to improve survival rates and quality of life for locally advanced pancreatic cancer patients. The company continues to enroll patients for the TIGeR-PaC study and anticipates releasing interim data soon.
- RenovoTAMP therapy platform shows potential to minimize chemotherapy side effects.
- Preliminary data indicates a two-thirds reduction in systemic gemcitabine levels, suggesting improved targeting.
- Ongoing enrollment in Phase 3 TIGeR-PaC clinical trial may suggest strong investor confidence.
- None.
Presentation Featured RenovoTAMP™ (RenovoRx Trans-Arterial Micro-Perfusion) and the Phase 3 TIGeR-PaC Clinical Trial
Since 2018,
Dr. Gandhi’s presentation at the 2022
“We appreciate
View Dr. Gandhi’s presentation, titled “Trans-arterial Treatment Option in Pancreas Cancer,” at https://renovorx.com.
About the 2022
The SPECTRUM conference offers attendees a comprehensive review of a variety of oncological diseases, combined with the latest developments in medical, interventional and surgical therapeutic options across multiple disciplines. SPECTRUM is both didactic and interactive with panel discussions, instructive case presentations and hands-on workshops focused on hepatocellular carcinoma, lung cancer, metastatic colorectal cancer, cholangiocarcinoma and liver metastases, renal and prostate cancer, pancreatic cancer, neuroendocrine and musculoskeletal tumors.
About
RenovoRx’s patent portfolio includes seven
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Forward-Looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, and Section 21E of the Securities Exchange Act of 1934, including but not limited to statements regarding our Phase 1 (RR1) and Observational Registry (RR2) studies, statements regarding the potential of RenovoTAMPTM, RenovoCath® or RenovoGemTM or regarding our ongoing TIGeR-PaC Phase 3 clinical trial in LAPC, and statements regarding the potential for our product candidates to treat or provide clinically meaningful outcomes for certain medical conditions or diseases. Statements that are not purely historical are forward-looking statements. The forward-looking statements contained herein are based upon our current expectations and beliefs regarding future events, many of which, by their nature, are inherently uncertain, outside of our control and involve assumptions that may never materialize or may prove to be incorrect. These may include estimates, projections and statements relating to our research and development plans, clinical trials, therapy platform, business plans, objectives and expected operating results, which are based on current expectations and assumptions that are subject to known and unknown risks and uncertainties that may cause actual results to differ materially from those expressed or implied by these forward-looking statements. These statements may be identified using words such as “may,” “expects,” “plans,” “aims,” “anticipates,” “believes,” “forecasts,” “estimates,” “intends,” and “potential,” or the negative of these terms or other comparable terminology regarding RenovoRx’s expectations strategy, plans or intentions, although not all forward-looking statements contain these words. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, that could cause actual events to differ materially from those projected or indicated by such statements, including, among other things: the timing of the initiation, progress and potential results of our preclinical studies, clinical trials and our research programs; our ability to use and expand our therapy platform to build a pipeline of product candidates; our ability to advance product candidates into, and successfully complete, clinical trials; the timing or likelihood of regulatory filings and approvals; our estimates of the number of patients who suffer from the diseases we are targeting and the number of patients that may enroll in our clinical trials; the commercialization potential of our product candidates, if approved; our ability and the potential to successfully manufacture and supply our product candidates for clinical trials and for commercial use, if approved; future strategic arrangements and/or collaborations and the potential benefits of such arrangements; our estimates regarding expenses, future revenue, capital requirements and needs for additional financing and our ability to obtain additional capital; the sufficiency of our existing cash and cash equivalents to fund our future operating expenses and capital expenditure requirements; our ability to retain the continued service of our key personnel and to identify, hire and retain additional qualified personnel; the implementation of our strategic plans for our business and product candidates; the scope of protection we are able to establish and maintain for intellectual property rights, including our therapy platform, product candidates and research programs; our ability to contract with third-party suppliers and manufacturers and their ability to perform adequately; the pricing, coverage and reimbursement of our product candidates, if approved; developments relating to our competitors and our industry, including competing product candidates and therapies; negative impacts of the COVID-19 pandemic on our operations; and other risks.
Information regarding the foregoing and additional risks may be found in the section entitled “Risk Factors” in documents that we file from time to time with the
Forward-looking statements included herein are made as of the date hereof, and
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FAQ
What is RenovoRx's RenovoTAMP therapy and how does it work?
What were the results of the Phase 3 TIGeR-PaC clinical trial presentation at the 2022 SPECTRUM Conference?
When is the interim data readout for the TIGeR-PaC clinical trial expected?
How does RenovoTAMP improve patient outcomes for those with locally advanced pancreatic cancer?